Name: rs33924202
Published: September 21, 2022
License: Open Access

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.

rs33924202

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:44379731-44379751 (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: del(T)₁₃ / del(T)₁₂ / del(T)₈ / de…
del(T)₁₃ / del(T)₁₂ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₆
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₃=0.000008 (2/264690, TOPMED)
delTT=0.1034 (803/7766, ALFA)
(T)₂₁=0.3115 (1560/5008, 1000G)

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	7766	TTTTTTTTTTTTTTTTTTTTT=0.8217	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.1034, TTTTTTTTTTTTTTTTTTTT=0.0734, TTTTTTTTTTTTTTTTTTTTTT=0.0015, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.823757	0.022923	0.153319	32
European	Sub	6878	TTTTTTTTTTTTTTTTTTTTT=0.7988	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.1167, TTTTTTTTTTTTTTTTTTTT=0.0827, TTTTTTTTTTTTTTTTTTTTTT=0.0017, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.796982	0.026406	0.176612	27
African	Sub	636	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	22	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	614	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	8	TTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	6	TTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	2	TTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	36	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	82	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	12	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	114	TTTTTTTTTTTTTTTTTTTTT=0.991	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.009, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A

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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(T)₂₁=0.999992	del(T)₁₃=0.000008
Allele Frequency Aggregator	Total	Global	7766	(T)₂₁=0.8217	del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, delTTT=0.0000, delTT=0.1034, delT=0.0734, dupT=0.0015, dupTT=0.0000
Allele Frequency Aggregator	European	Sub	6878	(T)₂₁=0.7988	del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, delTTT=0.0000, delTT=0.1167, delT=0.0827, dupT=0.0017, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	636	(T)₂₁=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	114	(T)₂₁=0.991	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.009, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	82	(T)₂₁=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	36	(T)₂₁=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	12	(T)₂₁=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Asian	Sub	8	(T)₂₁=1.0	del(T)₁₃=0.0, del(T)₁₂=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0
1000Genomes	Global	Study-wide	5008	(T)₂₁=0.3115	delTT=0.6885
1000Genomes	African	Sub	1322	(T)₂₁=0.2315	delTT=0.7685
1000Genomes	East Asian	Sub	1008	(T)₂₁=0.2222	delTT=0.7778
1000Genomes	Europe	Sub	1006	(T)₂₁=0.5338	delTT=0.4662
1000Genomes	South Asian	Sub	978	(T)₂₁=0.287	delTT=0.713
1000Genomes	American	Sub	694	(T)₂₁=0.305	delTT=0.695

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.44379739_44379751del
GRCh38.p14 chr 20	NC_000020.11:g.44379740_44379751del
GRCh38.p14 chr 20	NC_000020.11:g.44379744_44379751del
GRCh38.p14 chr 20	NC_000020.11:g.44379745_44379751del
GRCh38.p14 chr 20	NC_000020.11:g.44379746_44379751del
GRCh38.p14 chr 20	NC_000020.11:g.44379747_44379751del
GRCh38.p14 chr 20	NC_000020.11:g.44379748_44379751del
GRCh38.p14 chr 20	NC_000020.11:g.44379749_44379751del
GRCh38.p14 chr 20	NC_000020.11:g.44379750_44379751del
GRCh38.p14 chr 20	NC_000020.11:g.44379751del
GRCh38.p14 chr 20	NC_000020.11:g.44379751dup
GRCh38.p14 chr 20	NC_000020.11:g.44379750_44379751dup
GRCh38.p14 chr 20	NC_000020.11:g.44379749_44379751dup
GRCh38.p14 chr 20	NC_000020.11:g.44379748_44379751dup
GRCh38.p14 chr 20	NC_000020.11:g.44379746_44379751dup
GRCh37.p13 chr 20	NC_000020.10:g.43008379_43008391del
GRCh37.p13 chr 20	NC_000020.10:g.43008380_43008391del
GRCh37.p13 chr 20	NC_000020.10:g.43008384_43008391del
GRCh37.p13 chr 20	NC_000020.10:g.43008385_43008391del
GRCh37.p13 chr 20	NC_000020.10:g.43008386_43008391del
GRCh37.p13 chr 20	NC_000020.10:g.43008387_43008391del
GRCh37.p13 chr 20	NC_000020.10:g.43008388_43008391del
GRCh37.p13 chr 20	NC_000020.10:g.43008389_43008391del
GRCh37.p13 chr 20	NC_000020.10:g.43008390_43008391del
GRCh37.p13 chr 20	NC_000020.10:g.43008391del
GRCh37.p13 chr 20	NC_000020.10:g.43008391dup
GRCh37.p13 chr 20	NC_000020.10:g.43008390_43008391dup
GRCh37.p13 chr 20	NC_000020.10:g.43008389_43008391dup
GRCh37.p13 chr 20	NC_000020.10:g.43008388_43008391dup
GRCh37.p13 chr 20	NC_000020.10:g.43008386_43008391dup
HNF4A RefSeqGene (LRG_483)	NG_009818.1:g.28939_28951del
HNF4A RefSeqGene (LRG_483)	NG_009818.1:g.28940_28951del
HNF4A RefSeqGene (LRG_483)	NG_009818.1:g.28944_28951del
HNF4A RefSeqGene (LRG_483)	NG_009818.1:g.28945_28951del
HNF4A RefSeqGene (LRG_483)	NG_009818.1:g.28946_28951del
HNF4A RefSeqGene (LRG_483)	NG_009818.1:g.28947_28951del
HNF4A RefSeqGene (LRG_483)	NG_009818.1:g.28948_28951del
HNF4A RefSeqGene (LRG_483)	NG_009818.1:g.28949_28951del
HNF4A RefSeqGene (LRG_483)	NG_009818.1:g.28950_28951del
HNF4A RefSeqGene (LRG_483)	NG_009818.1:g.28951del
HNF4A RefSeqGene (LRG_483)	NG_009818.1:g.28951dup
HNF4A RefSeqGene (LRG_483)	NG_009818.1:g.28950_28951dup
HNF4A RefSeqGene (LRG_483)	NG_009818.1:g.28949_28951dup
HNF4A RefSeqGene (LRG_483)	NG_009818.1:g.28948_28951dup
HNF4A RefSeqGene (LRG_483)	NG_009818.1:g.28946_28951dup

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.49+23886… NM_001030003.3:c.49+23886_49+23898del	N/A	Intron Variant
HNF4A transcript variant 6	NM_001030004.3:c.49+23886… NM_001030004.3:c.49+23886_49+23898del	N/A	Intron Variant
HNF4A transcript variant 8	NM_001287182.2:c.-182-107… NM_001287182.2:c.-182-10719_-182-10707del	N/A	Intron Variant
HNF4A transcript variant 9	NM_001287183.2:c.-182-107… NM_001287183.2:c.-182-10719_-182-10707del	N/A	Intron Variant
HNF4A transcript variant 10	NM_001287184.2:c.-182-107… NM_001287184.2:c.-182-10719_-182-10707del	N/A	Intron Variant
HNF4A transcript variant 5	NM_175914.5:c.49+23886_49… NM_175914.5:c.49+23886_49+23898del	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.-1326-20… XM_047440135.1:c.-1326-20141_-1326-20129del	N/A	Intron Variant
HNF4A transcript variant X2	XM_047440136.1:c.-1102-20… XM_047440136.1:c.-1102-20141_-1102-20129del	N/A	Intron Variant
HNF4A transcript variant X3	XM_047440137.1:c.-922-207… XM_047440137.1:c.-922-20712_-922-20700del	N/A	Intron Variant
HNF4A transcript variant X4	XM_047440138.1:c.-1493-20… XM_047440138.1:c.-1493-20141_-1493-20129del	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

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

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)₂₁=	del(T)₁₃	del(T)₁₂	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₆
GRCh38.p14 chr 20	NC_000020.11:g.44379731_44379751=	NC_000020.11:g.44379739_44379751del	NC_000020.11:g.44379740_44379751del	NC_000020.11:g.44379744_44379751del	NC_000020.11:g.44379745_44379751del	NC_000020.11:g.44379746_44379751del	NC_000020.11:g.44379747_44379751del	NC_000020.11:g.44379748_44379751del	NC_000020.11:g.44379749_44379751del	NC_000020.11:g.44379750_44379751del	NC_000020.11:g.44379751del	NC_000020.11:g.44379751dup	NC_000020.11:g.44379750_44379751dup	NC_000020.11:g.44379749_44379751dup	NC_000020.11:g.44379748_44379751dup	NC_000020.11:g.44379746_44379751dup
GRCh37.p13 chr 20	NC_000020.10:g.43008371_43008391=	NC_000020.10:g.43008379_43008391del	NC_000020.10:g.43008380_43008391del	NC_000020.10:g.43008384_43008391del	NC_000020.10:g.43008385_43008391del	NC_000020.10:g.43008386_43008391del	NC_000020.10:g.43008387_43008391del	NC_000020.10:g.43008388_43008391del	NC_000020.10:g.43008389_43008391del	NC_000020.10:g.43008390_43008391del	NC_000020.10:g.43008391del	NC_000020.10:g.43008391dup	NC_000020.10:g.43008390_43008391dup	NC_000020.10:g.43008389_43008391dup	NC_000020.10:g.43008388_43008391dup	NC_000020.10:g.43008386_43008391dup
HNF4A RefSeqGene (LRG_483)	NG_009818.1:g.28931_28951=	NG_009818.1:g.28939_28951del	NG_009818.1:g.28940_28951del	NG_009818.1:g.28944_28951del	NG_009818.1:g.28945_28951del	NG_009818.1:g.28946_28951del	NG_009818.1:g.28947_28951del	NG_009818.1:g.28948_28951del	NG_009818.1:g.28949_28951del	NG_009818.1:g.28950_28951del	NG_009818.1:g.28951del	NG_009818.1:g.28951dup	NG_009818.1:g.28950_28951dup	NG_009818.1:g.28949_28951dup	NG_009818.1:g.28948_28951dup	NG_009818.1:g.28946_28951dup
HNF4A transcript variant 4	NM_001030003.2:c.49+23878=	NM_001030003.2:c.49+23886_49+23898del	NM_001030003.2:c.49+23887_49+23898del	NM_001030003.2:c.49+23891_49+23898del	NM_001030003.2:c.49+23892_49+23898del	NM_001030003.2:c.49+23893_49+23898del	NM_001030003.2:c.49+23894_49+23898del	NM_001030003.2:c.49+23895_49+23898del	NM_001030003.2:c.49+23896_49+23898del	NM_001030003.2:c.49+23897_49+23898del	NM_001030003.2:c.49+23898del	NM_001030003.2:c.49+23898dup	NM_001030003.2:c.49+23897_49+23898dup	NM_001030003.2:c.49+23896_49+23898dup	NM_001030003.2:c.49+23895_49+23898dup	NM_001030003.2:c.49+23893_49+23898dup
HNF4A transcript variant 4	NM_001030003.3:c.49+23878=	NM_001030003.3:c.49+23886_49+23898del	NM_001030003.3:c.49+23887_49+23898del	NM_001030003.3:c.49+23891_49+23898del	NM_001030003.3:c.49+23892_49+23898del	NM_001030003.3:c.49+23893_49+23898del	NM_001030003.3:c.49+23894_49+23898del	NM_001030003.3:c.49+23895_49+23898del	NM_001030003.3:c.49+23896_49+23898del	NM_001030003.3:c.49+23897_49+23898del	NM_001030003.3:c.49+23898del	NM_001030003.3:c.49+23898dup	NM_001030003.3:c.49+23897_49+23898dup	NM_001030003.3:c.49+23896_49+23898dup	NM_001030003.3:c.49+23895_49+23898dup	NM_001030003.3:c.49+23893_49+23898dup
HNF4A transcript variant 6	NM_001030004.2:c.49+23878=	NM_001030004.2:c.49+23886_49+23898del	NM_001030004.2:c.49+23887_49+23898del	NM_001030004.2:c.49+23891_49+23898del	NM_001030004.2:c.49+23892_49+23898del	NM_001030004.2:c.49+23893_49+23898del	NM_001030004.2:c.49+23894_49+23898del	NM_001030004.2:c.49+23895_49+23898del	NM_001030004.2:c.49+23896_49+23898del	NM_001030004.2:c.49+23897_49+23898del	NM_001030004.2:c.49+23898del	NM_001030004.2:c.49+23898dup	NM_001030004.2:c.49+23897_49+23898dup	NM_001030004.2:c.49+23896_49+23898dup	NM_001030004.2:c.49+23895_49+23898dup	NM_001030004.2:c.49+23893_49+23898dup
HNF4A transcript variant 6	NM_001030004.3:c.49+23878=	NM_001030004.3:c.49+23886_49+23898del	NM_001030004.3:c.49+23887_49+23898del	NM_001030004.3:c.49+23891_49+23898del	NM_001030004.3:c.49+23892_49+23898del	NM_001030004.3:c.49+23893_49+23898del	NM_001030004.3:c.49+23894_49+23898del	NM_001030004.3:c.49+23895_49+23898del	NM_001030004.3:c.49+23896_49+23898del	NM_001030004.3:c.49+23897_49+23898del	NM_001030004.3:c.49+23898del	NM_001030004.3:c.49+23898dup	NM_001030004.3:c.49+23897_49+23898dup	NM_001030004.3:c.49+23896_49+23898dup	NM_001030004.3:c.49+23895_49+23898dup	NM_001030004.3:c.49+23893_49+23898dup
HNF4A transcript variant 8	NM_001287182.2:c.-182-10727=	NM_001287182.2:c.-182-10719_-182-10707del	NM_001287182.2:c.-182-10718_-182-10707del	NM_001287182.2:c.-182-10714_-182-10707del	NM_001287182.2:c.-182-10713_-182-10707del	NM_001287182.2:c.-182-10712_-182-10707del	NM_001287182.2:c.-182-10711_-182-10707del	NM_001287182.2:c.-182-10710_-182-10707del	NM_001287182.2:c.-182-10709_-182-10707del	NM_001287182.2:c.-182-10708_-182-10707del	NM_001287182.2:c.-182-10707del	NM_001287182.2:c.-182-10707dup	NM_001287182.2:c.-182-10708_-182-10707dup	NM_001287182.2:c.-182-10709_-182-10707dup	NM_001287182.2:c.-182-10710_-182-10707dup	NM_001287182.2:c.-182-10712_-182-10707dup
HNF4A transcript variant 9	NM_001287183.2:c.-182-10727=	NM_001287183.2:c.-182-10719_-182-10707del	NM_001287183.2:c.-182-10718_-182-10707del	NM_001287183.2:c.-182-10714_-182-10707del	NM_001287183.2:c.-182-10713_-182-10707del	NM_001287183.2:c.-182-10712_-182-10707del	NM_001287183.2:c.-182-10711_-182-10707del	NM_001287183.2:c.-182-10710_-182-10707del	NM_001287183.2:c.-182-10709_-182-10707del	NM_001287183.2:c.-182-10708_-182-10707del	NM_001287183.2:c.-182-10707del	NM_001287183.2:c.-182-10707dup	NM_001287183.2:c.-182-10708_-182-10707dup	NM_001287183.2:c.-182-10709_-182-10707dup	NM_001287183.2:c.-182-10710_-182-10707dup	NM_001287183.2:c.-182-10712_-182-10707dup
HNF4A transcript variant 10	NM_001287184.2:c.-182-10727=	NM_001287184.2:c.-182-10719_-182-10707del	NM_001287184.2:c.-182-10718_-182-10707del	NM_001287184.2:c.-182-10714_-182-10707del	NM_001287184.2:c.-182-10713_-182-10707del	NM_001287184.2:c.-182-10712_-182-10707del	NM_001287184.2:c.-182-10711_-182-10707del	NM_001287184.2:c.-182-10710_-182-10707del	NM_001287184.2:c.-182-10709_-182-10707del	NM_001287184.2:c.-182-10708_-182-10707del	NM_001287184.2:c.-182-10707del	NM_001287184.2:c.-182-10707dup	NM_001287184.2:c.-182-10708_-182-10707dup	NM_001287184.2:c.-182-10709_-182-10707dup	NM_001287184.2:c.-182-10710_-182-10707dup	NM_001287184.2:c.-182-10712_-182-10707dup
HNF4A transcript variant 5	NM_175914.4:c.49+23878=	NM_175914.4:c.49+23886_49+23898del	NM_175914.4:c.49+23887_49+23898del	NM_175914.4:c.49+23891_49+23898del	NM_175914.4:c.49+23892_49+23898del	NM_175914.4:c.49+23893_49+23898del	NM_175914.4:c.49+23894_49+23898del	NM_175914.4:c.49+23895_49+23898del	NM_175914.4:c.49+23896_49+23898del	NM_175914.4:c.49+23897_49+23898del	NM_175914.4:c.49+23898del	NM_175914.4:c.49+23898dup	NM_175914.4:c.49+23897_49+23898dup	NM_175914.4:c.49+23896_49+23898dup	NM_175914.4:c.49+23895_49+23898dup	NM_175914.4:c.49+23893_49+23898dup
HNF4A transcript variant 5	NM_175914.5:c.49+23878=	NM_175914.5:c.49+23886_49+23898del	NM_175914.5:c.49+23887_49+23898del	NM_175914.5:c.49+23891_49+23898del	NM_175914.5:c.49+23892_49+23898del	NM_175914.5:c.49+23893_49+23898del	NM_175914.5:c.49+23894_49+23898del	NM_175914.5:c.49+23895_49+23898del	NM_175914.5:c.49+23896_49+23898del	NM_175914.5:c.49+23897_49+23898del	NM_175914.5:c.49+23898del	NM_175914.5:c.49+23898dup	NM_175914.5:c.49+23897_49+23898dup	NM_175914.5:c.49+23896_49+23898dup	NM_175914.5:c.49+23895_49+23898dup	NM_175914.5:c.49+23893_49+23898dup
HNF4A transcript variant X1	XM_047440135.1:c.-1326-20149=	XM_047440135.1:c.-1326-20141_-1326-20129del	XM_047440135.1:c.-1326-20140_-1326-20129del	XM_047440135.1:c.-1326-20136_-1326-20129del	XM_047440135.1:c.-1326-20135_-1326-20129del	XM_047440135.1:c.-1326-20134_-1326-20129del	XM_047440135.1:c.-1326-20133_-1326-20129del	XM_047440135.1:c.-1326-20132_-1326-20129del	XM_047440135.1:c.-1326-20131_-1326-20129del	XM_047440135.1:c.-1326-20130_-1326-20129del	XM_047440135.1:c.-1326-20129del	XM_047440135.1:c.-1326-20129dup	XM_047440135.1:c.-1326-20130_-1326-20129dup	XM_047440135.1:c.-1326-20131_-1326-20129dup	XM_047440135.1:c.-1326-20132_-1326-20129dup	XM_047440135.1:c.-1326-20134_-1326-20129dup
HNF4A transcript variant X2	XM_047440136.1:c.-1102-20149=	XM_047440136.1:c.-1102-20141_-1102-20129del	XM_047440136.1:c.-1102-20140_-1102-20129del	XM_047440136.1:c.-1102-20136_-1102-20129del	XM_047440136.1:c.-1102-20135_-1102-20129del	XM_047440136.1:c.-1102-20134_-1102-20129del	XM_047440136.1:c.-1102-20133_-1102-20129del	XM_047440136.1:c.-1102-20132_-1102-20129del	XM_047440136.1:c.-1102-20131_-1102-20129del	XM_047440136.1:c.-1102-20130_-1102-20129del	XM_047440136.1:c.-1102-20129del	XM_047440136.1:c.-1102-20129dup	XM_047440136.1:c.-1102-20130_-1102-20129dup	XM_047440136.1:c.-1102-20131_-1102-20129dup	XM_047440136.1:c.-1102-20132_-1102-20129dup	XM_047440136.1:c.-1102-20134_-1102-20129dup
HNF4A transcript variant X3	XM_047440137.1:c.-922-20720=	XM_047440137.1:c.-922-20712_-922-20700del	XM_047440137.1:c.-922-20711_-922-20700del	XM_047440137.1:c.-922-20707_-922-20700del	XM_047440137.1:c.-922-20706_-922-20700del	XM_047440137.1:c.-922-20705_-922-20700del	XM_047440137.1:c.-922-20704_-922-20700del	XM_047440137.1:c.-922-20703_-922-20700del	XM_047440137.1:c.-922-20702_-922-20700del	XM_047440137.1:c.-922-20701_-922-20700del	XM_047440137.1:c.-922-20700del	XM_047440137.1:c.-922-20700dup	XM_047440137.1:c.-922-20701_-922-20700dup	XM_047440137.1:c.-922-20702_-922-20700dup	XM_047440137.1:c.-922-20703_-922-20700dup	XM_047440137.1:c.-922-20705_-922-20700dup
HNF4A transcript variant X4	XM_047440138.1:c.-1493-20149=	XM_047440138.1:c.-1493-20141_-1493-20129del	XM_047440138.1:c.-1493-20140_-1493-20129del	XM_047440138.1:c.-1493-20136_-1493-20129del	XM_047440138.1:c.-1493-20135_-1493-20129del	XM_047440138.1:c.-1493-20134_-1493-20129del	XM_047440138.1:c.-1493-20133_-1493-20129del	XM_047440138.1:c.-1493-20132_-1493-20129del	XM_047440138.1:c.-1493-20131_-1493-20129del	XM_047440138.1:c.-1493-20130_-1493-20129del	XM_047440138.1:c.-1493-20129del	XM_047440138.1:c.-1493-20129dup	XM_047440138.1:c.-1493-20130_-1493-20129dup	XM_047440138.1:c.-1493-20131_-1493-20129dup	XM_047440138.1:c.-1493-20132_-1493-20129dup	XM_047440138.1:c.-1493-20134_-1493-20129dup

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#.

48 SubSNP, 26 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41359501	Dec 03, 2013 (142)
2	ABI	ss41399021	Dec 03, 2013 (142)
3	HGSV	ss80877344	Dec 15, 2007 (131)
4	HUMANGENOME_JCVI	ss95740832	Dec 05, 2013 (142)
5	HUMANGENOME_JCVI	ss96245739	Dec 05, 2013 (142)
6	PJP	ss295049676	Sep 08, 2015 (146)
7	PJP	ss295049677	May 09, 2011 (134)
8	1000GENOMES	ss1378510148	Aug 21, 2014 (142)
9	SWEGEN	ss3018235137	Nov 08, 2017 (151)
10	EVA_DECODE	ss3707010923	Jul 13, 2019 (153)
11	EVA_DECODE	ss3707010924	Jul 13, 2019 (153)
12	EVA_DECODE	ss3707010925	Jul 13, 2019 (153)
13	EVA_DECODE	ss3707010926	Jul 13, 2019 (153)
14	EVA_DECODE	ss3707010927	Jul 13, 2019 (153)
15	KHV_HUMAN_GENOMES	ss3821844681	Jul 13, 2019 (153)
16	EVA	ss3835687917	Apr 27, 2020 (154)
17	GNOMAD	ss4353983537	Apr 27, 2021 (155)
18	GNOMAD	ss4353983538	Apr 27, 2021 (155)
19	GNOMAD	ss4353983539	Apr 27, 2021 (155)
20	GNOMAD	ss4353983540	Apr 27, 2021 (155)
21	GNOMAD	ss4353983541	Apr 27, 2021 (155)
22	GNOMAD	ss4353983543	Apr 27, 2021 (155)
23	GNOMAD	ss4353983544	Apr 27, 2021 (155)
24	GNOMAD	ss4353983545	Apr 27, 2021 (155)
25	GNOMAD	ss4353983546	Apr 27, 2021 (155)
26	GNOMAD	ss4353983547	Apr 27, 2021 (155)
27	GNOMAD	ss4353983548	Apr 27, 2021 (155)
28	GNOMAD	ss4353983549	Apr 27, 2021 (155)
29	GNOMAD	ss4353983550	Apr 27, 2021 (155)
30	TOPMED	ss5089794708	Apr 27, 2021 (155)
31	TOMMO_GENOMICS	ss5229800009	Apr 27, 2021 (155)
32	TOMMO_GENOMICS	ss5229800010	Apr 27, 2021 (155)
33	TOMMO_GENOMICS	ss5229800011	Apr 27, 2021 (155)
34	TOMMO_GENOMICS	ss5229800012	Apr 27, 2021 (155)
35	1000G_HIGH_COVERAGE	ss5308915225	Oct 16, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5308915226	Oct 16, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5308915227	Oct 16, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5308915228	Oct 16, 2022 (156)
39	HUGCELL_USP	ss5501182225	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5501182226	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5501182227	Oct 16, 2022 (156)
42	HUGCELL_USP	ss5501182228	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5789646075	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5789646076	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5789646077	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5789646078	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5789646079	Oct 16, 2022 (156)
48	EVA	ss5981089130	Oct 16, 2022 (156)
49	1000Genomes	NC_000020.10 - 43008371	Oct 12, 2018 (152)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 552832200 (NC_000020.11:44379730::T 554/100612) Row 552832201 (NC_000020.11:44379730::TT 32/100610) Row 552832202 (NC_000020.11:44379730::TTT 8/100622)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 552832200 (NC_000020.11:44379730::T 554/100612) Row 552832201 (NC_000020.11:44379730::TT 32/100610) Row 552832202 (NC_000020.11:44379730::TTT 8/100622)...	-	Apr 27, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 552832200 (NC_000020.11:44379730::T 554/100612) Row 552832201 (NC_000020.11:44379730::TT 32/100610) Row 552832202 (NC_000020.11:44379730::TTT 8/100622)...	-	Apr 27, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 552832200 (NC_000020.11:44379730::T 554/100612) Row 552832201 (NC_000020.11:44379730::TT 32/100610) Row 552832202 (NC_000020.11:44379730::TTT 8/100622)...	-	Apr 27, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 552832200 (NC_000020.11:44379730::T 554/100612) Row 552832201 (NC_000020.11:44379730::TT 32/100610) Row 552832202 (NC_000020.11:44379730::TTT 8/100622)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 552832200 (NC_000020.11:44379730::T 554/100612) Row 552832201 (NC_000020.11:44379730::TT 32/100610) Row 552832202 (NC_000020.11:44379730::TTT 8/100622)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 552832200 (NC_000020.11:44379730::T 554/100612) Row 552832201 (NC_000020.11:44379730::TT 32/100610) Row 552832202 (NC_000020.11:44379730::TTT 8/100622)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 552832200 (NC_000020.11:44379730::T 554/100612) Row 552832201 (NC_000020.11:44379730::TT 32/100610) Row 552832202 (NC_000020.11:44379730::TTT 8/100622)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 552832200 (NC_000020.11:44379730::T 554/100612) Row 552832201 (NC_000020.11:44379730::TT 32/100610) Row 552832202 (NC_000020.11:44379730::TTT 8/100622)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 552832200 (NC_000020.11:44379730::T 554/100612) Row 552832201 (NC_000020.11:44379730::TT 32/100610) Row 552832202 (NC_000020.11:44379730::TTT 8/100622)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 552832200 (NC_000020.11:44379730::T 554/100612) Row 552832201 (NC_000020.11:44379730::TT 32/100610) Row 552832202 (NC_000020.11:44379730::TTT 8/100622)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 552832200 (NC_000020.11:44379730::T 554/100612) Row 552832201 (NC_000020.11:44379730::TT 32/100610) Row 552832202 (NC_000020.11:44379730::TTT 8/100622)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 552832200 (NC_000020.11:44379730::T 554/100612) Row 552832201 (NC_000020.11:44379730::TT 32/100610) Row 552832202 (NC_000020.11:44379730::TTT 8/100622)...	-	Apr 27, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 552832200 (NC_000020.11:44379730::T 554/100612) Row 552832201 (NC_000020.11:44379730::TT 32/100610) Row 552832202 (NC_000020.11:44379730::TTT 8/100622)...	-	Apr 27, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 87769316 (NC_000020.10:43008370:T: 5332/16554) Row 87769317 (NC_000020.10:43008370:TT: 2916/16554) Row 87769318 (NC_000020.10:43008370:TTTTTTTT: 7/16554)...	-	Apr 27, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 87769316 (NC_000020.10:43008370:T: 5332/16554) Row 87769317 (NC_000020.10:43008370:TT: 2916/16554) Row 87769318 (NC_000020.10:43008370:TTTTTTTT: 7/16554)...	-	Apr 27, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 87769316 (NC_000020.10:43008370:T: 5332/16554) Row 87769317 (NC_000020.10:43008370:TT: 2916/16554) Row 87769318 (NC_000020.10:43008370:TTTTTTTT: 7/16554)...	-	Apr 27, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 87769316 (NC_000020.10:43008370:T: 5332/16554) Row 87769317 (NC_000020.10:43008370:TT: 2916/16554) Row 87769318 (NC_000020.10:43008370:TTTTTTTT: 7/16554)...	-	Apr 27, 2021 (155)
68	14KJPN Submission ignored due to conflicting rows: Row 123483179 (NC_000020.11:44379730:TT: 4554/26324) Row 123483180 (NC_000020.11:44379730:T: 8351/26324) Row 123483181 (NC_000020.11:44379730:TTTTTTTT: 10/26324)...	-	Oct 16, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 123483179 (NC_000020.11:44379730:TT: 4554/26324) Row 123483180 (NC_000020.11:44379730:T: 8351/26324) Row 123483181 (NC_000020.11:44379730:TTTTTTTT: 10/26324)...	-	Oct 16, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 123483179 (NC_000020.11:44379730:TT: 4554/26324) Row 123483180 (NC_000020.11:44379730:T: 8351/26324) Row 123483181 (NC_000020.11:44379730:TTTTTTTT: 10/26324)...	-	Oct 16, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 123483179 (NC_000020.11:44379730:TT: 4554/26324) Row 123483180 (NC_000020.11:44379730:T: 8351/26324) Row 123483181 (NC_000020.11:44379730:TTTTTTTT: 10/26324)...	-	Oct 16, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 123483179 (NC_000020.11:44379730:TT: 4554/26324) Row 123483180 (NC_000020.11:44379730:T: 8351/26324) Row 123483181 (NC_000020.11:44379730:TTTTTTTT: 10/26324)...	-	Oct 16, 2022 (156)
73	TopMed	NC_000020.11 - 44379731	Apr 27, 2021 (155)
74	ALFA	NC_000020.11 - 44379731	Apr 27, 2021 (155)

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).

Associated ID	History Updated (Build)
rs397864443	Aug 21, 2014 (142)
rs58790053	Dec 02, 2009 (131)
rs397716136	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
364903653, ss5089794708	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTT:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
5043000744	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTT	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
ss4353983550	NC_000020.11:44379730:TTTTTTTTTTTT:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
5043000744	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss5229800011	NC_000020.10:43008370:TTTTTTTT:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4353983549, ss5789646077	NC_000020.11:44379730:TTTTTTTT:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
5043000744	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4353983548	NC_000020.11:44379730:TTTTTTT:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
5043000744	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4353983547	NC_000020.11:44379730:TTTTTT:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
5043000744	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4353983546	NC_000020.11:44379730:TTTTT:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
5043000744	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3707010923, ss4353983545	NC_000020.11:44379730:TTTT:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5229800012	NC_000020.10:43008370:TTT:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4353983544, ss5308915227, ss5501182228, ss5789646078	NC_000020.11:44379730:TTT:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
5043000744	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3707010924	NC_000020.11:44379731:TTT:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss295049676	NC_000020.9:42441803:TT:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
78372568, ss1378510148, ss3018235137, ss3835687917, ss5229800010, ss5981089130	NC_000020.10:43008370:TT:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3821844681, ss4353983543, ss5308915226, ss5501182225, ss5789646075	NC_000020.11:44379730:TT:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
5043000744	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3707010925	NC_000020.11:44379732:TT:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss41359501	NT_011362.10:13204481:TT:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss80877344, ss295049677	NC_000020.9:42441804:T:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5229800009	NC_000020.10:43008370:T:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5308915225, ss5501182227, ss5789646076	NC_000020.11:44379730:T:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
5043000744	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3707010926	NC_000020.11:44379733:T:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss41359501	NT_011362.10:13204481:TT:T	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss41399021, ss95740832, ss96245739	NT_011362.10:13204482:T:	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4353983537, ss5308915228, ss5501182226, ss5789646079	NC_000020.11:44379730::T	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
5043000744	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3707010927	NC_000020.11:44379734::T	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353983538	NC_000020.11:44379730::TT	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
5043000744	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353983539	NC_000020.11:44379730::TTT	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353983540	NC_000020.11:44379730::TTTT	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353983541	NC_000020.11:44379730::TTTTTT	NC_000020.11:44379730:TTTTTTTTTTTT… NC_000020.11:44379730:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

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

No publications for rs33924202

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs33924202