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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs1491454694

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr20:44385058 (GRCh38.p14) Help

The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.

Alleles
insA(T)6 / insA(T)13 / insA(T)16 /…

insA(T)6 / insA(T)13 / insA(T)16 / insG(T)16 / insG(T)33 / dupT / insTT / insTTT / ins(T)4 / ins(T)5 / ins(T)6 / ins(T)7 / ins(T)8 / ins(T)9 / ins(T)10 / ins(T)11 / ins(T)12 / ins(T)13 / ins(T)14 / ins(T)15 / ins(T)16 / ins(T)17 / ins(T)18 / ins(T)20 / ins(T)21 / ins(T)22 / ins(T)23 / ins(T)24 / ins(T)25 / ins(T)27 / ins(T)28 / ins(T)30 / ins(T)31

Variation Type
Indel Insertion and Deletion
Frequency
ins(T)5=0.00005 (1/18456, ALFA)
ins(T)11=0.0006 (1/1736, Korea1K)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
HNF4A : Intron Variant
HNF4A-AS1 : Intron Variant
Publications
0 citations
Genomic View
See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315
Population Group Sample Size Ref Allele Alt Allele Ref HMOZ Alt HMOZ HTRZ HWEP
Total Global 18456 T=0.99995 TT=0.00000, TTT=0.00000, TTTT=0.00000, TTTTT=0.00000, TTTTTT=0.00005 0.999892 0.0 0.000108 0
European Sub 14088 T=0.99993 TT=0.00000, TTT=0.00000, TTTT=0.00000, TTTTT=0.00000, TTTTTT=0.00007 0.999858 0.0 0.000142 0
African Sub 2898 T=1.0000 TT=0.0000, TTT=0.0000, TTTT=0.0000, TTTTT=0.0000, TTTTTT=0.0000 1.0 0.0 0.0 N/A
African Others Sub 114 T=1.000 TT=0.000, TTT=0.000, TTTT=0.000, TTTTT=0.000, TTTTTT=0.000 1.0 0.0 0.0 N/A
African American Sub 2784 T=1.0000 TT=0.0000, TTT=0.0000, TTTT=0.0000, TTTTT=0.0000, TTTTTT=0.0000 1.0 0.0 0.0 N/A
Asian Sub 112 T=1.000 TT=0.000, TTT=0.000, TTTT=0.000, TTTTT=0.000, TTTTTT=0.000 1.0 0.0 0.0 N/A
East Asian Sub 86 T=1.00 TT=0.00, TTT=0.00, TTTT=0.00, TTTTT=0.00, TTTTTT=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 26 T=1.00 TT=0.00, TTT=0.00, TTTT=0.00, TTTTT=0.00, TTTTTT=0.00 1.0 0.0 0.0 N/A
Latin American 1 Sub 146 T=1.000 TT=0.000, TTT=0.000, TTTT=0.000, TTTTT=0.000, TTTTTT=0.000 1.0 0.0 0.0 N/A
Latin American 2 Sub 610 T=1.000 TT=0.000, TTT=0.000, TTTT=0.000, TTTTT=0.000, TTTTTT=0.000 1.0 0.0 0.0 N/A
South Asian Sub 98 T=1.00 TT=0.00, TTT=0.00, TTTT=0.00, TTTTT=0.00, TTTTTT=0.00 1.0 0.0 0.0 N/A
Other Sub 504 T=1.000 TT=0.000, TTT=0.000, TTTT=0.000, TTTTT=0.000, TTTTTT=0.000 1.0 0.0 0.0 N/A


Help

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download
Study Population Group Sample Size Ref Allele Alt Allele
Allele Frequency Aggregator Total Global 18456 T=0.99995 dupT=0.00000, insTT=0.00000, insTTT=0.00000, ins(T)4=0.00000, ins(T)5=0.00005
Allele Frequency Aggregator European Sub 14088 T=0.99993 dupT=0.00000, insTT=0.00000, insTTT=0.00000, ins(T)4=0.00000, ins(T)5=0.00007
Allele Frequency Aggregator African Sub 2898 T=1.0000 dupT=0.0000, insTT=0.0000, insTTT=0.0000, ins(T)4=0.0000, ins(T)5=0.0000
Allele Frequency Aggregator Latin American 2 Sub 610 T=1.000 dupT=0.000, insTT=0.000, insTTT=0.000, ins(T)4=0.000, ins(T)5=0.000
Allele Frequency Aggregator Other Sub 504 T=1.000 dupT=0.000, insTT=0.000, insTTT=0.000, ins(T)4=0.000, ins(T)5=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 T=1.000 dupT=0.000, insTT=0.000, insTTT=0.000, ins(T)4=0.000, ins(T)5=0.000
Allele Frequency Aggregator Asian Sub 112 T=1.000 dupT=0.000, insTT=0.000, insTTT=0.000, ins(T)4=0.000, ins(T)5=0.000
Allele Frequency Aggregator South Asian Sub 98 T=1.00 dupT=0.00, insTT=0.00, insTTT=0.00, ins(T)4=0.00, ins(T)5=0.00
Korean Genome Project KOREAN Study-wide 1736 -

No frequency provided

 ins(T)11=0.0006
Help

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements
Sequence name Change
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insATTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insATTTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insATTTTTTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insGTTTTTTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058dup
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 20 NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insATTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insATTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insATTTTTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insGTTTTTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698dup
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insATTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insATTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insATTTTTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insGTTTTTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258dup
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene: HNF4A, hepatocyte nuclear factor 4 alpha (plus strand)
Molecule type Change Amino acid[Codon] SO Term
HNF4A transcript variant 4 NM_001030003.3:c.50-21000…

NM_001030003.3:c.50-21000_50-20999insATTTTTT

 		N/A Intron Variant
HNF4A transcript variant 6 NM_001030004.3:c.50-21000…

NM_001030004.3:c.50-21000_50-20999insATTTTTT

 		N/A Intron Variant
HNF4A transcript variant 8 NM_001287182.2:c.-182-540…

NM_001287182.2:c.-182-5400_-182-5399insATTTTTT

 		N/A Intron Variant
HNF4A transcript variant 9 NM_001287183.2:c.-182-540…

NM_001287183.2:c.-182-5400_-182-5399insATTTTTT

 		N/A Intron Variant
HNF4A transcript variant 10 NM_001287184.2:c.-182-540…

NM_001287184.2:c.-182-5400_-182-5399insATTTTTT

 		N/A Intron Variant
HNF4A transcript variant 5 NM_175914.5:c.50-21000_50…

NM_175914.5:c.50-21000_50-20999insATTTTTT

 		N/A Intron Variant
HNF4A transcript variant 2 NM_000457.6:c. N/A Genic Upstream Transcript Variant
HNF4A transcript variant 7 NM_001258355.2:c. N/A Genic Upstream Transcript Variant
HNF4A transcript variant 1 NM_178849.3:c. N/A Genic Upstream Transcript Variant
HNF4A transcript variant 3 NM_178850.3:c. N/A Genic Upstream Transcript Variant
HNF4A transcript variant X1 XM_047440135.1:c.-1326-14…

XM_047440135.1:c.-1326-14822_-1326-14821insATTTTTT

 		N/A Intron Variant
HNF4A transcript variant X2 XM_047440136.1:c.-1102-14…

XM_047440136.1:c.-1102-14822_-1102-14821insATTTTTT

 		N/A Intron Variant
HNF4A transcript variant X3 XM_047440137.1:c.-922-153…

XM_047440137.1:c.-922-15393_-922-15392insATTTTTT

 		N/A Intron Variant
HNF4A transcript variant X4 XM_047440138.1:c.-1493-14…

XM_047440138.1:c.-1493-14822_-1493-14821insATTTTTT

 		N/A Intron Variant
Gene: HNF4A-AS1, HNF4A antisense RNA 1 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
HNF4A-AS1 transcript variant 1 NR_109949.1:n. N/A Intron Variant
HNF4A-AS1 transcript variant 2 NR_172878.1:n. N/A Intron Variant
HNF4A-AS1 transcript variant 3 NR_172879.1:n. N/A Intron Variant
Help

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar
Help

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement T= insA(T)6 insA(T)13 insA(T)16 insG(T)16 insG(T)33 dupT insTT insTTT ins(T)4 ins(T)5 ins(T)6 ins(T)7 ins(T)8 ins(T)9 ins(T)10 ins(T)11 ins(T)12 ins(T)13 ins(T)14 ins(T)15 ins(T)16 ins(T)17 ins(T)18 ins(T)20 ins(T)21 ins(T)22 ins(T)23 ins(T)24 ins(T)25 ins(T)27 ins(T)28 ins(T)30 ins(T)31
GRCh38.p14 chr 20 NC_000020.11:g.44385058= NC_000020.11:g.44385058_44385059insATTTTTT NC_000020.11:g.44385058_44385059insATTTTTTTTTTTTT NC_000020.11:g.44385058_44385059insATTTTTTTTTTTTTTTT NC_000020.11:g.44385058_44385059insGTTTTTTTTTTTTTTTT NC_000020.11:g.44385058_44385059insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000020.11:g.44385058dup NC_000020.11:g.44385058_44385059insTT NC_000020.11:g.44385058_44385059insTTT NC_000020.11:g.44385058_44385059insTTTT NC_000020.11:g.44385058_44385059insTTTTT NC_000020.11:g.44385058_44385059insTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTTTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000020.11:g.44385058_44385059insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 20 NC_000020.10:g.43013698= NC_000020.10:g.43013698_43013699insATTTTTT NC_000020.10:g.43013698_43013699insATTTTTTTTTTTTT NC_000020.10:g.43013698_43013699insATTTTTTTTTTTTTTTT NC_000020.10:g.43013698_43013699insGTTTTTTTTTTTTTTTT NC_000020.10:g.43013698_43013699insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000020.10:g.43013698dup NC_000020.10:g.43013698_43013699insTT NC_000020.10:g.43013698_43013699insTTT NC_000020.10:g.43013698_43013699insTTTT NC_000020.10:g.43013698_43013699insTTTTT NC_000020.10:g.43013698_43013699insTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTTTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000020.10:g.43013698_43013699insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.34258= NG_009818.1:g.34258_34259insATTTTTT NG_009818.1:g.34258_34259insATTTTTTTTTTTTT NG_009818.1:g.34258_34259insATTTTTTTTTTTTTTTT NG_009818.1:g.34258_34259insGTTTTTTTTTTTTTTTT NG_009818.1:g.34258_34259insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NG_009818.1:g.34258dup NG_009818.1:g.34258_34259insTT NG_009818.1:g.34258_34259insTTT NG_009818.1:g.34258_34259insTTTT NG_009818.1:g.34258_34259insTTTTT NG_009818.1:g.34258_34259insTTTTTT NG_009818.1:g.34258_34259insTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTTTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTTTTTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NG_009818.1:g.34258_34259insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A transcript variant 4 NM_001030003.2:c.50-21000= NM_001030003.2:c.50-21000_50-20999insATTTTTT NM_001030003.2:c.50-21000_50-20999insATTTTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insATTTTTTTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insGTTTTTTTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001030003.2:c.50-21000dup NM_001030003.2:c.50-21000_50-20999insTT NM_001030003.2:c.50-21000_50-20999insTTT NM_001030003.2:c.50-21000_50-20999insTTTT NM_001030003.2:c.50-21000_50-20999insTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001030003.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A transcript variant 4 NM_001030003.3:c.50-21000= NM_001030003.3:c.50-21000_50-20999insATTTTTT NM_001030003.3:c.50-21000_50-20999insATTTTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insATTTTTTTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insGTTTTTTTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001030003.3:c.50-21000dup NM_001030003.3:c.50-21000_50-20999insTT NM_001030003.3:c.50-21000_50-20999insTTT NM_001030003.3:c.50-21000_50-20999insTTTT NM_001030003.3:c.50-21000_50-20999insTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001030003.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A transcript variant 6 NM_001030004.2:c.50-21000= NM_001030004.2:c.50-21000_50-20999insATTTTTT NM_001030004.2:c.50-21000_50-20999insATTTTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insATTTTTTTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insGTTTTTTTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001030004.2:c.50-21000dup NM_001030004.2:c.50-21000_50-20999insTT NM_001030004.2:c.50-21000_50-20999insTTT NM_001030004.2:c.50-21000_50-20999insTTTT NM_001030004.2:c.50-21000_50-20999insTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001030004.2:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A transcript variant 6 NM_001030004.3:c.50-21000= NM_001030004.3:c.50-21000_50-20999insATTTTTT NM_001030004.3:c.50-21000_50-20999insATTTTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insATTTTTTTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insGTTTTTTTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001030004.3:c.50-21000dup NM_001030004.3:c.50-21000_50-20999insTT NM_001030004.3:c.50-21000_50-20999insTTT NM_001030004.3:c.50-21000_50-20999insTTTT NM_001030004.3:c.50-21000_50-20999insTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001030004.3:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A transcript variant 8 NM_001287182.2:c.-182-5400= NM_001287182.2:c.-182-5400_-182-5399insATTTTTT NM_001287182.2:c.-182-5400_-182-5399insATTTTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insATTTTTTTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insGTTTTTTTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001287182.2:c.-182-5400dup NM_001287182.2:c.-182-5400_-182-5399insTT NM_001287182.2:c.-182-5400_-182-5399insTTT NM_001287182.2:c.-182-5400_-182-5399insTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001287182.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A transcript variant 9 NM_001287183.2:c.-182-5400= NM_001287183.2:c.-182-5400_-182-5399insATTTTTT NM_001287183.2:c.-182-5400_-182-5399insATTTTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insATTTTTTTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insGTTTTTTTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001287183.2:c.-182-5400dup NM_001287183.2:c.-182-5400_-182-5399insTT NM_001287183.2:c.-182-5400_-182-5399insTTT NM_001287183.2:c.-182-5400_-182-5399insTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001287183.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A transcript variant 10 NM_001287184.2:c.-182-5400= NM_001287184.2:c.-182-5400_-182-5399insATTTTTT NM_001287184.2:c.-182-5400_-182-5399insATTTTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insATTTTTTTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insGTTTTTTTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001287184.2:c.-182-5400dup NM_001287184.2:c.-182-5400_-182-5399insTT NM_001287184.2:c.-182-5400_-182-5399insTTT NM_001287184.2:c.-182-5400_-182-5399insTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_001287184.2:c.-182-5400_-182-5399insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A transcript variant 5 NM_175914.4:c.50-21000= NM_175914.4:c.50-21000_50-20999insATTTTTT NM_175914.4:c.50-21000_50-20999insATTTTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insATTTTTTTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insGTTTTTTTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_175914.4:c.50-21000dup NM_175914.4:c.50-21000_50-20999insTT NM_175914.4:c.50-21000_50-20999insTTT NM_175914.4:c.50-21000_50-20999insTTTT NM_175914.4:c.50-21000_50-20999insTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_175914.4:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A transcript variant 5 NM_175914.5:c.50-21000= NM_175914.5:c.50-21000_50-20999insATTTTTT NM_175914.5:c.50-21000_50-20999insATTTTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insATTTTTTTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insGTTTTTTTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_175914.5:c.50-21000dup NM_175914.5:c.50-21000_50-20999insTT NM_175914.5:c.50-21000_50-20999insTTT NM_175914.5:c.50-21000_50-20999insTTTT NM_175914.5:c.50-21000_50-20999insTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NM_175914.5:c.50-21000_50-20999insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A transcript variant X1 XM_047440135.1:c.-1326-14822= XM_047440135.1:c.-1326-14822_-1326-14821insATTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insATTTTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insATTTTTTTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insGTTTTTTTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XM_047440135.1:c.-1326-14822dup XM_047440135.1:c.-1326-14822_-1326-14821insTT XM_047440135.1:c.-1326-14822_-1326-14821insTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTTTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTTTTTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTTTTTTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTTTTTTTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTTTTTTTTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTTTTTTTTTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTTTTTTTTTTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTTTTTTTTTTTTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTTTTTTTTTTTTTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XM_047440135.1:c.-1326-14822_-1326-14821insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A transcript variant X2 XM_047440136.1:c.-1102-14822= XM_047440136.1:c.-1102-14822_-1102-14821insATTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insATTTTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insATTTTTTTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insGTTTTTTTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XM_047440136.1:c.-1102-14822dup XM_047440136.1:c.-1102-14822_-1102-14821insTT XM_047440136.1:c.-1102-14822_-1102-14821insTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTTTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTTTTTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTTTTTTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTTTTTTTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTTTTTTTTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTTTTTTTTTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTTTTTTTTTTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTTTTTTTTTTTTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTTTTTTTTTTTTTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XM_047440136.1:c.-1102-14822_-1102-14821insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A transcript variant X3 XM_047440137.1:c.-922-15393= XM_047440137.1:c.-922-15393_-922-15392insATTTTTT XM_047440137.1:c.-922-15393_-922-15392insATTTTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insATTTTTTTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insGTTTTTTTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XM_047440137.1:c.-922-15393dup XM_047440137.1:c.-922-15393_-922-15392insTT XM_047440137.1:c.-922-15393_-922-15392insTTT XM_047440137.1:c.-922-15393_-922-15392insTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTTTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTTTTTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTTTTTTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTTTTTTTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTTTTTTTTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTTTTTTTTTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTTTTTTTTTTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTTTTTTTTTTTTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTTTTTTTTTTTTTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XM_047440137.1:c.-922-15393_-922-15392insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
HNF4A transcript variant X4 XM_047440138.1:c.-1493-14822= XM_047440138.1:c.-1493-14822_-1493-14821insATTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insATTTTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insATTTTTTTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insGTTTTTTTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XM_047440138.1:c.-1493-14822dup XM_047440138.1:c.-1493-14822_-1493-14821insTT XM_047440138.1:c.-1493-14822_-1493-14821insTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTTTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTTTTTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTTTTTTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTTTTTTTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTTTTTTTTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTTTTTTTTTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTTTTTTTTTTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTTTTTTTTTTTTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTTTTTTTTTTTTTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XM_047440138.1:c.-1493-14822_-1493-14821insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Help

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

42 SubSNP, 41 Frequency submissions
No Submitter Submission ID Date (Build)
1 KOGIC ss3982346552 Apr 27, 2020 (154)
2 GNOMAD ss4353984182 Apr 27, 2021 (155)
3 GNOMAD ss4353984183 Apr 27, 2021 (155)
4 GNOMAD ss4353984184 Apr 27, 2021 (155)
5 GNOMAD ss4353984185 Apr 27, 2021 (155)
6 GNOMAD ss4353984186 Apr 27, 2021 (155)
7 GNOMAD ss4353984187 Apr 27, 2021 (155)
8 GNOMAD ss4353984188 Apr 27, 2021 (155)
9 GNOMAD ss4353984189 Apr 27, 2021 (155)
10 GNOMAD ss4353984190 Apr 27, 2021 (155)
11 GNOMAD ss4353984191 Apr 27, 2021 (155)
12 GNOMAD ss4353984192 Apr 27, 2021 (155)
13 GNOMAD ss4353984193 Apr 27, 2021 (155)
14 GNOMAD ss4353984194 Apr 27, 2021 (155)
15 GNOMAD ss4353984195 Apr 27, 2021 (155)
16 GNOMAD ss4353984196 Apr 27, 2021 (155)
17 GNOMAD ss4353984197 Apr 27, 2021 (155)
18 GNOMAD ss4353984198 Apr 27, 2021 (155)
19 GNOMAD ss4353984199 Apr 27, 2021 (155)
20 GNOMAD ss4353984200 Apr 27, 2021 (155)
21 GNOMAD ss4353984201 Apr 27, 2021 (155)
22 GNOMAD ss4353984202 Apr 27, 2021 (155)
23 GNOMAD ss4353984203 Apr 27, 2021 (155)
24 GNOMAD ss4353984204 Apr 27, 2021 (155)
25 GNOMAD ss4353984205 Apr 27, 2021 (155)
26 GNOMAD ss4353984206 Apr 27, 2021 (155)
27 GNOMAD ss4353984207 Apr 27, 2021 (155)
28 GNOMAD ss4353984208 Apr 27, 2021 (155)
29 GNOMAD ss4353984209 Apr 27, 2021 (155)
30 GNOMAD ss4353984210 Apr 27, 2021 (155)
31 GNOMAD ss4353984211 Apr 27, 2021 (155)
32 GNOMAD ss4353984212 Apr 27, 2021 (155)
33 TOMMO_GENOMICS ss5229800224 Apr 27, 2021 (155)
34 TOMMO_GENOMICS ss5229800225 Apr 27, 2021 (155)
35 TOMMO_GENOMICS ss5229800226 Apr 27, 2021 (155)
36 TOMMO_GENOMICS ss5229800227 Apr 27, 2021 (155)
37 HUGCELL_USP ss5501182364 Oct 16, 2022 (156)
38 TOMMO_GENOMICS ss5789646349 Oct 16, 2022 (156)
39 TOMMO_GENOMICS ss5789646351 Oct 16, 2022 (156)
40 TOMMO_GENOMICS ss5789646352 Oct 16, 2022 (156)
41 TOMMO_GENOMICS ss5789646353 Oct 16, 2022 (156)
42 YY_MCH ss5818071931 Oct 16, 2022 (156)
43 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
44 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
45 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
46 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
47 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
48 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
49 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
50 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
51 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
52 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
53 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
54 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
55 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
56 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
57 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
58 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
59 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
60 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
61 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
62 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
63 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
64 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
65 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
66 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
67 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
68 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
69 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
70 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
71 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
72 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
73 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 552833301 (NC_000020.11:44385057::T 19/28522)
Row 552833302 (NC_000020.11:44385057::TATTTTTTTTTTTT 1/28548)
Row 552833303 (NC_000020.11:44385057::TATTTTTTTTTTTTTTT 2/28548)...

- Apr 27, 2021 (155)
74 Korean Genome Project NC_000020.11 - 44385058 Apr 27, 2020 (154)
75 8.3KJPN

Submission ignored due to conflicting rows:
Row 87769531 (NC_000020.10:43013697::TTTTTTTTTTTTTT 2/16010)
Row 87769532 (NC_000020.10:43013697::TTTTTTTTTTTTTTTTTT 1/16010)
Row 87769533 (NC_000020.10:43013697::TTTTTTTTTTTTTTTTT 1/16010)...

- Apr 27, 2021 (155)
76 8.3KJPN

Submission ignored due to conflicting rows:
Row 87769531 (NC_000020.10:43013697::TTTTTTTTTTTTTT 2/16010)
Row 87769532 (NC_000020.10:43013697::TTTTTTTTTTTTTTTTTT 1/16010)
Row 87769533 (NC_000020.10:43013697::TTTTTTTTTTTTTTTTT 1/16010)...

- Apr 27, 2021 (155)
77 8.3KJPN

Submission ignored due to conflicting rows:
Row 87769531 (NC_000020.10:43013697::TTTTTTTTTTTTTT 2/16010)
Row 87769532 (NC_000020.10:43013697::TTTTTTTTTTTTTTTTTT 1/16010)
Row 87769533 (NC_000020.10:43013697::TTTTTTTTTTTTTTTTT 1/16010)...

- Apr 27, 2021 (155)
78 8.3KJPN

Submission ignored due to conflicting rows:
Row 87769531 (NC_000020.10:43013697::TTTTTTTTTTTTTT 2/16010)
Row 87769532 (NC_000020.10:43013697::TTTTTTTTTTTTTTTTTT 1/16010)
Row 87769533 (NC_000020.10:43013697::TTTTTTTTTTTTTTTTT 1/16010)...

- Apr 27, 2021 (155)
79 14KJPN

Submission ignored due to conflicting rows:
Row 123483453 (NC_000020.11:44385057::TTTTTTTTTTTTTT 2/25484)
Row 123483455 (NC_000020.11:44385057::TTTTTTTTTTTTTTTTT 1/25484)
Row 123483456 (NC_000020.11:44385057::TATTTTT 1/25484)...

- Oct 16, 2022 (156)
80 14KJPN

Submission ignored due to conflicting rows:
Row 123483453 (NC_000020.11:44385057::TTTTTTTTTTTTTT 2/25484)
Row 123483455 (NC_000020.11:44385057::TTTTTTTTTTTTTTTTT 1/25484)
Row 123483456 (NC_000020.11:44385057::TATTTTT 1/25484)...

- Oct 16, 2022 (156)
81 14KJPN

Submission ignored due to conflicting rows:
Row 123483453 (NC_000020.11:44385057::TTTTTTTTTTTTTT 2/25484)
Row 123483455 (NC_000020.11:44385057::TTTTTTTTTTTTTTTTT 1/25484)
Row 123483456 (NC_000020.11:44385057::TATTTTT 1/25484)...

- Oct 16, 2022 (156)
82 14KJPN

Submission ignored due to conflicting rows:
Row 123483453 (NC_000020.11:44385057::TTTTTTTTTTTTTT 2/25484)
Row 123483455 (NC_000020.11:44385057::TTTTTTTTTTTTTTTTT 1/25484)
Row 123483456 (NC_000020.11:44385057::TATTTTT 1/25484)...

- Oct 16, 2022 (156)
83 ALFA NC_000020.11 - 44385058 Apr 27, 2021 (155)
Help

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss5789646352 NC_000020.11:44385057::TATTTTT NC_000020.11:44385057:T:TATTTTTT
ss4353984183 NC_000020.11:44385057::TATTTTTTTTT…

NC_000020.11:44385057::TATTTTTTTTTTTT

 NC_000020.11:44385057:T:TATTTTTTTT…

NC_000020.11:44385057:T:TATTTTTTTTTTTTT

 (self)
ss4353984184 NC_000020.11:44385057::TATTTTTTTTT…

NC_000020.11:44385057::TATTTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TATTTTTTTT…

NC_000020.11:44385057:T:TATTTTTTTTTTTTTTTT

 (self)
ss4353984185 NC_000020.11:44385057::TGTTTTTTTTT…

NC_000020.11:44385057::TGTTTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TGTTTTTTTT…

NC_000020.11:44385057:T:TGTTTTTTTTTTTTTTTT

 (self)
ss4353984186 NC_000020.11:44385057::TGTTTTTTTTT…

NC_000020.11:44385057::TGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TGTTTTTTTT…

NC_000020.11:44385057:T:TGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

 (self)
ss4353984182 NC_000020.11:44385057::T NC_000020.11:44385057:T:TT (self)
11646885105 NC_000020.11:44385057:T:TT NC_000020.11:44385057:T:TT (self)
ss4353984187 NC_000020.11:44385057::TT NC_000020.11:44385057:T:TTT (self)
11646885105 NC_000020.11:44385057:T:TTT NC_000020.11:44385057:T:TTT (self)
ss4353984188 NC_000020.11:44385057::TTT NC_000020.11:44385057:T:TTTT (self)
11646885105 NC_000020.11:44385057:T:TTTT NC_000020.11:44385057:T:TTTT (self)
ss4353984189 NC_000020.11:44385057::TTTT NC_000020.11:44385057:T:TTTTT (self)
11646885105 NC_000020.11:44385057:T:TTTTT NC_000020.11:44385057:T:TTTTT (self)
ss4353984190 NC_000020.11:44385057::TTTTT NC_000020.11:44385057:T:TTTTTT (self)
11646885105 NC_000020.11:44385057:T:TTTTTT NC_000020.11:44385057:T:TTTTTT (self)
ss4353984191 NC_000020.11:44385057::TTTTTT NC_000020.11:44385057:T:TTTTTTT (self)
ss4353984192 NC_000020.11:44385057::TTTTTTT NC_000020.11:44385057:T:TTTTTTTT (self)
ss4353984193 NC_000020.11:44385057::TTTTTTTT NC_000020.11:44385057:T:TTTTTTTTT (self)
ss4353984194 NC_000020.11:44385057::TTTTTTTTT NC_000020.11:44385057:T:TTTTTTTTTT (self)
ss4353984195 NC_000020.11:44385057::TTTTTTTTTT NC_000020.11:44385057:T:TTTTTTTTTTT (self)
38724553, ss3982346552, ss4353984196, ss5818071931 NC_000020.11:44385057::TTTTTTTTTTT NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTT

 (self)
ss5229800227 NC_000020.10:43013697::TTTTTTTTTTTT NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTT

 (self)
ss4353984197 NC_000020.11:44385057::TTTTTTTTTTTT NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTT

 (self)
ss4353984198 NC_000020.11:44385057::TTTTTTTTTTT…

NC_000020.11:44385057::TTTTTTTTTTTTT

 NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTTT

 (self)
ss5229800224 NC_000020.10:43013697::TTTTTTTTTTT…

NC_000020.10:43013697::TTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTTTT

 (self)
ss4353984199, ss5789646349 NC_000020.11:44385057::TTTTTTTTTTT…

NC_000020.11:44385057::TTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTTTT

 (self)
ss4353984200 NC_000020.11:44385057::TTTTTTTTTTT…

NC_000020.11:44385057::TTTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTTTTT

 (self)
ss4353984201 NC_000020.11:44385057::TTTTTTTTTTT…

NC_000020.11:44385057::TTTTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTTTTTT

 (self)
ss5229800226 NC_000020.10:43013697::TTTTTTTTTTT…

NC_000020.10:43013697::TTTTTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTTTTTTT

 (self)
ss4353984202, ss5789646351 NC_000020.11:44385057::TTTTTTTTTTT…

NC_000020.11:44385057::TTTTTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTTTTTTT

 (self)
ss5229800225 NC_000020.10:43013697::TTTTTTTTTTT…

NC_000020.10:43013697::TTTTTTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTTTTTTTT

 (self)
ss4353984203 NC_000020.11:44385057::TTTTTTTTTTT…

NC_000020.11:44385057::TTTTTTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTTTTTTTT

 (self)
ss4353984204 NC_000020.11:44385057::TTTTTTTTTTT…

NC_000020.11:44385057::TTTTTTTTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTTTTTTTTTT

 (self)
ss4353984205 NC_000020.11:44385057::TTTTTTTTTTT…

NC_000020.11:44385057::TTTTTTTTTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTTTTTTTTTTT

 (self)
ss4353984206 NC_000020.11:44385057::TTTTTTTTTTT…

NC_000020.11:44385057::TTTTTTTTTTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTTTTTTTTTTTT

 (self)
ss4353984207 NC_000020.11:44385057::TTTTTTTTTTT…

NC_000020.11:44385057::TTTTTTTTTTTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTTTTTTTTTTTTT

 (self)
ss5501182364, ss5789646353 NC_000020.11:44385057::TTTTTTTTTTT…

NC_000020.11:44385057::TTTTTTTTTTTTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTTTTTTTTTTTTTT
ss4353984208 NC_000020.11:44385057::TTTTTTTTTTT…

NC_000020.11:44385057::TTTTTTTTTTTTTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTTTTTTTTTTTTTTT

 (self)
ss4353984209 NC_000020.11:44385057::TTTTTTTTTTT…

NC_000020.11:44385057::TTTTTTTTTTTTTTTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTTTTTTTTTTTTTTTTT

 (self)
ss4353984210 NC_000020.11:44385057::TTTTTTTTTTT…

NC_000020.11:44385057::TTTTTTTTTTTTTTTTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT

 (self)
ss4353984211 NC_000020.11:44385057::TTTTTTTTTTT…

NC_000020.11:44385057::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

 (self)
ss4353984212 NC_000020.11:44385057::TTTTTTTTTTT…

NC_000020.11:44385057::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

 NC_000020.11:44385057:T:TTTTTTTTTT…

NC_000020.11:44385057:T:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

 (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs1491454694

Help

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:
Select flank length:

Genomic regions, transcripts, and products
Top▲ Help

NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 2.0.1.post820+afb47a3d