Name: rs1199768843
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.

rs1199768843

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:35310645-35310668 (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(A)₁₁ / del(A)₁₀ / del(A)₇ / de…
del(A)₁₁ / del(A)₁₀ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₉
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₁=0.0000 (0/4400, ALFA)
del(A)₁₀=0.0000 (0/4400, ALFA)
del(A)₇=0.0000 (0/4400, ALFA) (+ 13 more)
del(A)₆=0.0000 (0/4400, ALFA)
del(A)₅=0.0000 (0/4400, ALFA)
del(A)₄=0.0000 (0/4400, ALFA)
delAAA=0.0000 (0/4400, ALFA)
delAA=0.0000 (0/4400, ALFA)
delA=0.0000 (0/4400, ALFA)
dupA=0.0000 (0/4400, ALFA)
dupAA=0.0000 (0/4400, ALFA)
dupAAA=0.0000 (0/4400, ALFA)
dup(A)₄=0.0000 (0/4400, ALFA)
dup(A)₅=0.0000 (0/4400, ALFA)
dup(A)₆=0.0000 (0/4400, ALFA)
dup(A)₉=0.0000 (0/4400, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: UQCC1 : 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	HWEP
Total	Global	4400	AAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	3200	AAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	562	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	16	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	546	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	58	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	48	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	10	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	48	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	330	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	22	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	180	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	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
Allele Frequency Aggregator	Total	Global	4400	(A)₂₄=1.0000	del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0000, dup(A)₉=0.0000
Allele Frequency Aggregator	European	Sub	3200	(A)₂₄=1.0000	del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0000, dup(A)₉=0.0000
Allele Frequency Aggregator	African	Sub	562	(A)₂₄=1.000	del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000, dup(A)₉=0.000
Allele Frequency Aggregator	Latin American 2	Sub	330	(A)₂₄=1.000	del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000, dup(A)₉=0.000
Allele Frequency Aggregator	Other	Sub	180	(A)₂₄=1.000	del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000, dup(A)₉=0.000
Allele Frequency Aggregator	Asian	Sub	58	(A)₂₄=1.00	del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₉=0.00
Allele Frequency Aggregator	Latin American 1	Sub	48	(A)₂₄=1.00	del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₉=0.00
Allele Frequency Aggregator	South Asian	Sub	22	(A)₂₄=1.00	del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₉=0.00

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.35310658_35310668del
GRCh38.p14 chr 20	NC_000020.11:g.35310659_35310668del
GRCh38.p14 chr 20	NC_000020.11:g.35310662_35310668del
GRCh38.p14 chr 20	NC_000020.11:g.35310663_35310668del
GRCh38.p14 chr 20	NC_000020.11:g.35310664_35310668del
GRCh38.p14 chr 20	NC_000020.11:g.35310665_35310668del
GRCh38.p14 chr 20	NC_000020.11:g.35310666_35310668del
GRCh38.p14 chr 20	NC_000020.11:g.35310667_35310668del
GRCh38.p14 chr 20	NC_000020.11:g.35310668del
GRCh38.p14 chr 20	NC_000020.11:g.35310668dup
GRCh38.p14 chr 20	NC_000020.11:g.35310667_35310668dup
GRCh38.p14 chr 20	NC_000020.11:g.35310666_35310668dup
GRCh38.p14 chr 20	NC_000020.11:g.35310665_35310668dup
GRCh38.p14 chr 20	NC_000020.11:g.35310664_35310668dup
GRCh38.p14 chr 20	NC_000020.11:g.35310663_35310668dup
GRCh38.p14 chr 20	NC_000020.11:g.35310662_35310668dup
GRCh38.p14 chr 20	NC_000020.11:g.35310660_35310668dup
GRCh37.p13 chr 20	NC_000020.10:g.33898461_33898471del
GRCh37.p13 chr 20	NC_000020.10:g.33898462_33898471del
GRCh37.p13 chr 20	NC_000020.10:g.33898465_33898471del
GRCh37.p13 chr 20	NC_000020.10:g.33898466_33898471del
GRCh37.p13 chr 20	NC_000020.10:g.33898467_33898471del
GRCh37.p13 chr 20	NC_000020.10:g.33898468_33898471del
GRCh37.p13 chr 20	NC_000020.10:g.33898469_33898471del
GRCh37.p13 chr 20	NC_000020.10:g.33898470_33898471del
GRCh37.p13 chr 20	NC_000020.10:g.33898471del
GRCh37.p13 chr 20	NC_000020.10:g.33898471dup
GRCh37.p13 chr 20	NC_000020.10:g.33898470_33898471dup
GRCh37.p13 chr 20	NC_000020.10:g.33898469_33898471dup
GRCh37.p13 chr 20	NC_000020.10:g.33898468_33898471dup
GRCh37.p13 chr 20	NC_000020.10:g.33898467_33898471dup
GRCh37.p13 chr 20	NC_000020.10:g.33898466_33898471dup
GRCh37.p13 chr 20	NC_000020.10:g.33898465_33898471dup
GRCh37.p13 chr 20	NC_000020.10:g.33898463_33898471dup
UQCC1 RefSeqGene	NG_021421.1:g.106488_106498del
UQCC1 RefSeqGene	NG_021421.1:g.106489_106498del
UQCC1 RefSeqGene	NG_021421.1:g.106492_106498del
UQCC1 RefSeqGene	NG_021421.1:g.106493_106498del
UQCC1 RefSeqGene	NG_021421.1:g.106494_106498del
UQCC1 RefSeqGene	NG_021421.1:g.106495_106498del
UQCC1 RefSeqGene	NG_021421.1:g.106496_106498del
UQCC1 RefSeqGene	NG_021421.1:g.106497_106498del
UQCC1 RefSeqGene	NG_021421.1:g.106498del
UQCC1 RefSeqGene	NG_021421.1:g.106498dup
UQCC1 RefSeqGene	NG_021421.1:g.106497_106498dup
UQCC1 RefSeqGene	NG_021421.1:g.106496_106498dup
UQCC1 RefSeqGene	NG_021421.1:g.106495_106498dup
UQCC1 RefSeqGene	NG_021421.1:g.106494_106498dup
UQCC1 RefSeqGene	NG_021421.1:g.106493_106498dup
UQCC1 RefSeqGene	NG_021421.1:g.106492_106498dup
UQCC1 RefSeqGene	NG_021421.1:g.106490_106498dup

Gene: UQCC1, ubiquinol-cytochrome c reductase complex assembly factor 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
UQCC1 transcript variant 3	NM_001184977.2:c.448-3876… NM_001184977.2:c.448-3876_448-3866del	N/A	Intron Variant
UQCC1 transcript variant 1	NM_018244.5:c.652-3876_65… NM_018244.5:c.652-3876_652-3866del	N/A	Intron Variant
UQCC1 transcript variant 2	NM_199487.3:c.574-3876_57… NM_199487.3:c.574-3876_574-3866del	N/A	Intron Variant
UQCC1 transcript variant X1	XM_011528877.2:c.694-3876… XM_011528877.2:c.694-3876_694-3866del	N/A	Intron Variant
UQCC1 transcript variant X2	XM_011528878.3:c.556-3876… XM_011528878.3:c.556-3876_556-3866del	N/A	Intron Variant
UQCC1 transcript variant X4	XM_011528879.2:c.514-3876… XM_011528879.2:c.514-3876_514-3866del	N/A	Intron Variant
UQCC1 transcript variant X3	XM_011528880.3:c.514-3876… XM_011528880.3:c.514-3876_514-3866del	N/A	Intron Variant
UQCC1 transcript variant X5	XM_011528881.4:c.355-3876… XM_011528881.4:c.355-3876_355-3866del	N/A	Intron Variant
UQCC1 transcript variant X6	XM_047440254.1:c.250-3876… XM_047440254.1:c.250-3876_250-3866del	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	(A)₂₄=	del(A)₁₁	del(A)₁₀	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₉
GRCh38.p14 chr 20	NC_000020.11:g.35310645_35310668=	NC_000020.11:g.35310658_35310668del	NC_000020.11:g.35310659_35310668del	NC_000020.11:g.35310662_35310668del	NC_000020.11:g.35310663_35310668del	NC_000020.11:g.35310664_35310668del	NC_000020.11:g.35310665_35310668del	NC_000020.11:g.35310666_35310668del	NC_000020.11:g.35310667_35310668del	NC_000020.11:g.35310668del	NC_000020.11:g.35310668dup	NC_000020.11:g.35310667_35310668dup	NC_000020.11:g.35310666_35310668dup	NC_000020.11:g.35310665_35310668dup	NC_000020.11:g.35310664_35310668dup	NC_000020.11:g.35310663_35310668dup	NC_000020.11:g.35310662_35310668dup	NC_000020.11:g.35310660_35310668dup
GRCh37.p13 chr 20	NC_000020.10:g.33898448_33898471=	NC_000020.10:g.33898461_33898471del	NC_000020.10:g.33898462_33898471del	NC_000020.10:g.33898465_33898471del	NC_000020.10:g.33898466_33898471del	NC_000020.10:g.33898467_33898471del	NC_000020.10:g.33898468_33898471del	NC_000020.10:g.33898469_33898471del	NC_000020.10:g.33898470_33898471del	NC_000020.10:g.33898471del	NC_000020.10:g.33898471dup	NC_000020.10:g.33898470_33898471dup	NC_000020.10:g.33898469_33898471dup	NC_000020.10:g.33898468_33898471dup	NC_000020.10:g.33898467_33898471dup	NC_000020.10:g.33898466_33898471dup	NC_000020.10:g.33898465_33898471dup	NC_000020.10:g.33898463_33898471dup
UQCC1 RefSeqGene	NG_021421.1:g.106475_106498=	NG_021421.1:g.106488_106498del	NG_021421.1:g.106489_106498del	NG_021421.1:g.106492_106498del	NG_021421.1:g.106493_106498del	NG_021421.1:g.106494_106498del	NG_021421.1:g.106495_106498del	NG_021421.1:g.106496_106498del	NG_021421.1:g.106497_106498del	NG_021421.1:g.106498del	NG_021421.1:g.106498dup	NG_021421.1:g.106497_106498dup	NG_021421.1:g.106496_106498dup	NG_021421.1:g.106495_106498dup	NG_021421.1:g.106494_106498dup	NG_021421.1:g.106493_106498dup	NG_021421.1:g.106492_106498dup	NG_021421.1:g.106490_106498dup
UQCC1 transcript variant 3	NM_001184977.1:c.448-3866=	NM_001184977.1:c.448-3876_448-3866del	NM_001184977.1:c.448-3875_448-3866del	NM_001184977.1:c.448-3872_448-3866del	NM_001184977.1:c.448-3871_448-3866del	NM_001184977.1:c.448-3870_448-3866del	NM_001184977.1:c.448-3869_448-3866del	NM_001184977.1:c.448-3868_448-3866del	NM_001184977.1:c.448-3867_448-3866del	NM_001184977.1:c.448-3866del	NM_001184977.1:c.448-3866dup	NM_001184977.1:c.448-3867_448-3866dup	NM_001184977.1:c.448-3868_448-3866dup	NM_001184977.1:c.448-3869_448-3866dup	NM_001184977.1:c.448-3870_448-3866dup	NM_001184977.1:c.448-3871_448-3866dup	NM_001184977.1:c.448-3872_448-3866dup	NM_001184977.1:c.448-3874_448-3866dup
UQCC1 transcript variant 3	NM_001184977.2:c.448-3866=	NM_001184977.2:c.448-3876_448-3866del	NM_001184977.2:c.448-3875_448-3866del	NM_001184977.2:c.448-3872_448-3866del	NM_001184977.2:c.448-3871_448-3866del	NM_001184977.2:c.448-3870_448-3866del	NM_001184977.2:c.448-3869_448-3866del	NM_001184977.2:c.448-3868_448-3866del	NM_001184977.2:c.448-3867_448-3866del	NM_001184977.2:c.448-3866del	NM_001184977.2:c.448-3866dup	NM_001184977.2:c.448-3867_448-3866dup	NM_001184977.2:c.448-3868_448-3866dup	NM_001184977.2:c.448-3869_448-3866dup	NM_001184977.2:c.448-3870_448-3866dup	NM_001184977.2:c.448-3871_448-3866dup	NM_001184977.2:c.448-3872_448-3866dup	NM_001184977.2:c.448-3874_448-3866dup
UQCC1 transcript variant 1	NM_018244.4:c.652-3866=	NM_018244.4:c.652-3876_652-3866del	NM_018244.4:c.652-3875_652-3866del	NM_018244.4:c.652-3872_652-3866del	NM_018244.4:c.652-3871_652-3866del	NM_018244.4:c.652-3870_652-3866del	NM_018244.4:c.652-3869_652-3866del	NM_018244.4:c.652-3868_652-3866del	NM_018244.4:c.652-3867_652-3866del	NM_018244.4:c.652-3866del	NM_018244.4:c.652-3866dup	NM_018244.4:c.652-3867_652-3866dup	NM_018244.4:c.652-3868_652-3866dup	NM_018244.4:c.652-3869_652-3866dup	NM_018244.4:c.652-3870_652-3866dup	NM_018244.4:c.652-3871_652-3866dup	NM_018244.4:c.652-3872_652-3866dup	NM_018244.4:c.652-3874_652-3866dup
UQCC1 transcript variant 1	NM_018244.5:c.652-3866=	NM_018244.5:c.652-3876_652-3866del	NM_018244.5:c.652-3875_652-3866del	NM_018244.5:c.652-3872_652-3866del	NM_018244.5:c.652-3871_652-3866del	NM_018244.5:c.652-3870_652-3866del	NM_018244.5:c.652-3869_652-3866del	NM_018244.5:c.652-3868_652-3866del	NM_018244.5:c.652-3867_652-3866del	NM_018244.5:c.652-3866del	NM_018244.5:c.652-3866dup	NM_018244.5:c.652-3867_652-3866dup	NM_018244.5:c.652-3868_652-3866dup	NM_018244.5:c.652-3869_652-3866dup	NM_018244.5:c.652-3870_652-3866dup	NM_018244.5:c.652-3871_652-3866dup	NM_018244.5:c.652-3872_652-3866dup	NM_018244.5:c.652-3874_652-3866dup
UQCC1 transcript variant 2	NM_199487.2:c.574-3866=	NM_199487.2:c.574-3876_574-3866del	NM_199487.2:c.574-3875_574-3866del	NM_199487.2:c.574-3872_574-3866del	NM_199487.2:c.574-3871_574-3866del	NM_199487.2:c.574-3870_574-3866del	NM_199487.2:c.574-3869_574-3866del	NM_199487.2:c.574-3868_574-3866del	NM_199487.2:c.574-3867_574-3866del	NM_199487.2:c.574-3866del	NM_199487.2:c.574-3866dup	NM_199487.2:c.574-3867_574-3866dup	NM_199487.2:c.574-3868_574-3866dup	NM_199487.2:c.574-3869_574-3866dup	NM_199487.2:c.574-3870_574-3866dup	NM_199487.2:c.574-3871_574-3866dup	NM_199487.2:c.574-3872_574-3866dup	NM_199487.2:c.574-3874_574-3866dup
UQCC1 transcript variant 2	NM_199487.3:c.574-3866=	NM_199487.3:c.574-3876_574-3866del	NM_199487.3:c.574-3875_574-3866del	NM_199487.3:c.574-3872_574-3866del	NM_199487.3:c.574-3871_574-3866del	NM_199487.3:c.574-3870_574-3866del	NM_199487.3:c.574-3869_574-3866del	NM_199487.3:c.574-3868_574-3866del	NM_199487.3:c.574-3867_574-3866del	NM_199487.3:c.574-3866del	NM_199487.3:c.574-3866dup	NM_199487.3:c.574-3867_574-3866dup	NM_199487.3:c.574-3868_574-3866dup	NM_199487.3:c.574-3869_574-3866dup	NM_199487.3:c.574-3870_574-3866dup	NM_199487.3:c.574-3871_574-3866dup	NM_199487.3:c.574-3872_574-3866dup	NM_199487.3:c.574-3874_574-3866dup
UQCC transcript variant X1	XM_005260440.1:c.694-3866=	XM_005260440.1:c.694-3876_694-3866del	XM_005260440.1:c.694-3875_694-3866del	XM_005260440.1:c.694-3872_694-3866del	XM_005260440.1:c.694-3871_694-3866del	XM_005260440.1:c.694-3870_694-3866del	XM_005260440.1:c.694-3869_694-3866del	XM_005260440.1:c.694-3868_694-3866del	XM_005260440.1:c.694-3867_694-3866del	XM_005260440.1:c.694-3866del	XM_005260440.1:c.694-3866dup	XM_005260440.1:c.694-3867_694-3866dup	XM_005260440.1:c.694-3868_694-3866dup	XM_005260440.1:c.694-3869_694-3866dup	XM_005260440.1:c.694-3870_694-3866dup	XM_005260440.1:c.694-3871_694-3866dup	XM_005260440.1:c.694-3872_694-3866dup	XM_005260440.1:c.694-3874_694-3866dup
UQCC transcript variant X2	XM_005260441.1:c.556-3866=	XM_005260441.1:c.556-3876_556-3866del	XM_005260441.1:c.556-3875_556-3866del	XM_005260441.1:c.556-3872_556-3866del	XM_005260441.1:c.556-3871_556-3866del	XM_005260441.1:c.556-3870_556-3866del	XM_005260441.1:c.556-3869_556-3866del	XM_005260441.1:c.556-3868_556-3866del	XM_005260441.1:c.556-3867_556-3866del	XM_005260441.1:c.556-3866del	XM_005260441.1:c.556-3866dup	XM_005260441.1:c.556-3867_556-3866dup	XM_005260441.1:c.556-3868_556-3866dup	XM_005260441.1:c.556-3869_556-3866dup	XM_005260441.1:c.556-3870_556-3866dup	XM_005260441.1:c.556-3871_556-3866dup	XM_005260441.1:c.556-3872_556-3866dup	XM_005260441.1:c.556-3874_556-3866dup
UQCC transcript variant X3	XM_005260442.1:c.316-3866=	XM_005260442.1:c.316-3876_316-3866del	XM_005260442.1:c.316-3875_316-3866del	XM_005260442.1:c.316-3872_316-3866del	XM_005260442.1:c.316-3871_316-3866del	XM_005260442.1:c.316-3870_316-3866del	XM_005260442.1:c.316-3869_316-3866del	XM_005260442.1:c.316-3868_316-3866del	XM_005260442.1:c.316-3867_316-3866del	XM_005260442.1:c.316-3866del	XM_005260442.1:c.316-3866dup	XM_005260442.1:c.316-3867_316-3866dup	XM_005260442.1:c.316-3868_316-3866dup	XM_005260442.1:c.316-3869_316-3866dup	XM_005260442.1:c.316-3870_316-3866dup	XM_005260442.1:c.316-3871_316-3866dup	XM_005260442.1:c.316-3872_316-3866dup	XM_005260442.1:c.316-3874_316-3866dup
UQCC transcript variant X4	XM_005260443.1:c.250-3866=	XM_005260443.1:c.250-3876_250-3866del	XM_005260443.1:c.250-3875_250-3866del	XM_005260443.1:c.250-3872_250-3866del	XM_005260443.1:c.250-3871_250-3866del	XM_005260443.1:c.250-3870_250-3866del	XM_005260443.1:c.250-3869_250-3866del	XM_005260443.1:c.250-3868_250-3866del	XM_005260443.1:c.250-3867_250-3866del	XM_005260443.1:c.250-3866del	XM_005260443.1:c.250-3866dup	XM_005260443.1:c.250-3867_250-3866dup	XM_005260443.1:c.250-3868_250-3866dup	XM_005260443.1:c.250-3869_250-3866dup	XM_005260443.1:c.250-3870_250-3866dup	XM_005260443.1:c.250-3871_250-3866dup	XM_005260443.1:c.250-3872_250-3866dup	XM_005260443.1:c.250-3874_250-3866dup
UQCC transcript variant X5	XM_005260444.1:c.241-3866=	XM_005260444.1:c.241-3876_241-3866del	XM_005260444.1:c.241-3875_241-3866del	XM_005260444.1:c.241-3872_241-3866del	XM_005260444.1:c.241-3871_241-3866del	XM_005260444.1:c.241-3870_241-3866del	XM_005260444.1:c.241-3869_241-3866del	XM_005260444.1:c.241-3868_241-3866del	XM_005260444.1:c.241-3867_241-3866del	XM_005260444.1:c.241-3866del	XM_005260444.1:c.241-3866dup	XM_005260444.1:c.241-3867_241-3866dup	XM_005260444.1:c.241-3868_241-3866dup	XM_005260444.1:c.241-3869_241-3866dup	XM_005260444.1:c.241-3870_241-3866dup	XM_005260444.1:c.241-3871_241-3866dup	XM_005260444.1:c.241-3872_241-3866dup	XM_005260444.1:c.241-3874_241-3866dup
UQCC1 transcript variant X1	XM_011528877.2:c.694-3866=	XM_011528877.2:c.694-3876_694-3866del	XM_011528877.2:c.694-3875_694-3866del	XM_011528877.2:c.694-3872_694-3866del	XM_011528877.2:c.694-3871_694-3866del	XM_011528877.2:c.694-3870_694-3866del	XM_011528877.2:c.694-3869_694-3866del	XM_011528877.2:c.694-3868_694-3866del	XM_011528877.2:c.694-3867_694-3866del	XM_011528877.2:c.694-3866del	XM_011528877.2:c.694-3866dup	XM_011528877.2:c.694-3867_694-3866dup	XM_011528877.2:c.694-3868_694-3866dup	XM_011528877.2:c.694-3869_694-3866dup	XM_011528877.2:c.694-3870_694-3866dup	XM_011528877.2:c.694-3871_694-3866dup	XM_011528877.2:c.694-3872_694-3866dup	XM_011528877.2:c.694-3874_694-3866dup
UQCC1 transcript variant X2	XM_011528878.3:c.556-3866=	XM_011528878.3:c.556-3876_556-3866del	XM_011528878.3:c.556-3875_556-3866del	XM_011528878.3:c.556-3872_556-3866del	XM_011528878.3:c.556-3871_556-3866del	XM_011528878.3:c.556-3870_556-3866del	XM_011528878.3:c.556-3869_556-3866del	XM_011528878.3:c.556-3868_556-3866del	XM_011528878.3:c.556-3867_556-3866del	XM_011528878.3:c.556-3866del	XM_011528878.3:c.556-3866dup	XM_011528878.3:c.556-3867_556-3866dup	XM_011528878.3:c.556-3868_556-3866dup	XM_011528878.3:c.556-3869_556-3866dup	XM_011528878.3:c.556-3870_556-3866dup	XM_011528878.3:c.556-3871_556-3866dup	XM_011528878.3:c.556-3872_556-3866dup	XM_011528878.3:c.556-3874_556-3866dup
UQCC1 transcript variant X4	XM_011528879.2:c.514-3866=	XM_011528879.2:c.514-3876_514-3866del	XM_011528879.2:c.514-3875_514-3866del	XM_011528879.2:c.514-3872_514-3866del	XM_011528879.2:c.514-3871_514-3866del	XM_011528879.2:c.514-3870_514-3866del	XM_011528879.2:c.514-3869_514-3866del	XM_011528879.2:c.514-3868_514-3866del	XM_011528879.2:c.514-3867_514-3866del	XM_011528879.2:c.514-3866del	XM_011528879.2:c.514-3866dup	XM_011528879.2:c.514-3867_514-3866dup	XM_011528879.2:c.514-3868_514-3866dup	XM_011528879.2:c.514-3869_514-3866dup	XM_011528879.2:c.514-3870_514-3866dup	XM_011528879.2:c.514-3871_514-3866dup	XM_011528879.2:c.514-3872_514-3866dup	XM_011528879.2:c.514-3874_514-3866dup
UQCC1 transcript variant X3	XM_011528880.3:c.514-3866=	XM_011528880.3:c.514-3876_514-3866del	XM_011528880.3:c.514-3875_514-3866del	XM_011528880.3:c.514-3872_514-3866del	XM_011528880.3:c.514-3871_514-3866del	XM_011528880.3:c.514-3870_514-3866del	XM_011528880.3:c.514-3869_514-3866del	XM_011528880.3:c.514-3868_514-3866del	XM_011528880.3:c.514-3867_514-3866del	XM_011528880.3:c.514-3866del	XM_011528880.3:c.514-3866dup	XM_011528880.3:c.514-3867_514-3866dup	XM_011528880.3:c.514-3868_514-3866dup	XM_011528880.3:c.514-3869_514-3866dup	XM_011528880.3:c.514-3870_514-3866dup	XM_011528880.3:c.514-3871_514-3866dup	XM_011528880.3:c.514-3872_514-3866dup	XM_011528880.3:c.514-3874_514-3866dup
UQCC1 transcript variant X5	XM_011528881.4:c.355-3866=	XM_011528881.4:c.355-3876_355-3866del	XM_011528881.4:c.355-3875_355-3866del	XM_011528881.4:c.355-3872_355-3866del	XM_011528881.4:c.355-3871_355-3866del	XM_011528881.4:c.355-3870_355-3866del	XM_011528881.4:c.355-3869_355-3866del	XM_011528881.4:c.355-3868_355-3866del	XM_011528881.4:c.355-3867_355-3866del	XM_011528881.4:c.355-3866del	XM_011528881.4:c.355-3866dup	XM_011528881.4:c.355-3867_355-3866dup	XM_011528881.4:c.355-3868_355-3866dup	XM_011528881.4:c.355-3869_355-3866dup	XM_011528881.4:c.355-3870_355-3866dup	XM_011528881.4:c.355-3871_355-3866dup	XM_011528881.4:c.355-3872_355-3866dup	XM_011528881.4:c.355-3874_355-3866dup
UQCC1 transcript variant X6	XM_047440254.1:c.250-3866=	XM_047440254.1:c.250-3876_250-3866del	XM_047440254.1:c.250-3875_250-3866del	XM_047440254.1:c.250-3872_250-3866del	XM_047440254.1:c.250-3871_250-3866del	XM_047440254.1:c.250-3870_250-3866del	XM_047440254.1:c.250-3869_250-3866del	XM_047440254.1:c.250-3868_250-3866del	XM_047440254.1:c.250-3867_250-3866del	XM_047440254.1:c.250-3866del	XM_047440254.1:c.250-3866dup	XM_047440254.1:c.250-3867_250-3866dup	XM_047440254.1:c.250-3868_250-3866dup	XM_047440254.1:c.250-3869_250-3866dup	XM_047440254.1:c.250-3870_250-3866dup	XM_047440254.1:c.250-3871_250-3866dup	XM_047440254.1:c.250-3872_250-3866dup	XM_047440254.1:c.250-3874_250-3866dup

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#.

43 SubSNP, 32 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss3018137901	Nov 08, 2017 (151)
2	MCHAISSO	ss3064854609	Jan 10, 2018 (151)
3	EVA_DECODE	ss3706888172	Jul 13, 2019 (153)
4	EVA_DECODE	ss3706888173	Jul 13, 2019 (153)
5	EVA_DECODE	ss3706888174	Jul 13, 2019 (153)
6	EVA_DECODE	ss3706888175	Jul 13, 2019 (153)
7	EVA_DECODE	ss3706888176	Jul 13, 2019 (153)
8	EVA_DECODE	ss3706888177	Jul 13, 2019 (153)
9	PACBIO	ss3793534105	Jul 13, 2019 (153)
10	PACBIO	ss3793534106	Jul 13, 2019 (153)
11	PACBIO	ss3798421004	Jul 13, 2019 (153)
12	PACBIO	ss3798421005	Jul 13, 2019 (153)
13	EVA	ss3835658811	Apr 27, 2020 (154)
14	KOGIC	ss3982220164	Apr 27, 2020 (154)
15	KOGIC	ss3982220165	Apr 27, 2020 (154)
16	KOGIC	ss3982220166	Apr 27, 2020 (154)
17	KOGIC	ss3982220167	Apr 27, 2020 (154)
18	KOGIC	ss3982220168	Apr 27, 2020 (154)
19	GNOMAD	ss4352883231	Apr 27, 2021 (155)
20	GNOMAD	ss4352883232	Apr 27, 2021 (155)
21	GNOMAD	ss4352883233	Apr 27, 2021 (155)
22	GNOMAD	ss4352883234	Apr 27, 2021 (155)
23	GNOMAD	ss4352883235	Apr 27, 2021 (155)
24	GNOMAD	ss4352883236	Apr 27, 2021 (155)
25	GNOMAD	ss4352883237	Apr 27, 2021 (155)
26	GNOMAD	ss4352883238	Apr 27, 2021 (155)
27	GNOMAD	ss4352883239	Apr 27, 2021 (155)
28	GNOMAD	ss4352883240	Apr 27, 2021 (155)
29	GNOMAD	ss4352883241	Apr 27, 2021 (155)
30	GNOMAD	ss4352883242	Apr 27, 2021 (155)
31	GNOMAD	ss4352883243	Apr 27, 2021 (155)
32	GNOMAD	ss4352883244	Apr 27, 2021 (155)
33	GNOMAD	ss4352883245	Apr 27, 2021 (155)
34	TOMMO_GENOMICS	ss5229511024	Apr 27, 2021 (155)
35	TOMMO_GENOMICS	ss5229511025	Apr 27, 2021 (155)
36	TOMMO_GENOMICS	ss5229511026	Apr 27, 2021 (155)
37	TOMMO_GENOMICS	ss5229511027	Apr 27, 2021 (155)
38	TOMMO_GENOMICS	ss5229511028	Apr 27, 2021 (155)
39	TOMMO_GENOMICS	ss5789268555	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5789268556	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5789268557	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5789268558	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5789268559	Oct 16, 2022 (156)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 550995995 (NC_000020.11:35310644::A 1477/41278) Row 550995996 (NC_000020.11:35310644::AA 12467/42334) Row 550995997 (NC_000020.11:35310644::AAA 601/42062)...	-	Apr 27, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 550995995 (NC_000020.11:35310644::A 1477/41278) Row 550995996 (NC_000020.11:35310644::AA 12467/42334) Row 550995997 (NC_000020.11:35310644::AAA 601/42062)...	-	Apr 27, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 550995995 (NC_000020.11:35310644::A 1477/41278) Row 550995996 (NC_000020.11:35310644::AA 12467/42334) Row 550995997 (NC_000020.11:35310644::AAA 601/42062)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 550995995 (NC_000020.11:35310644::A 1477/41278) Row 550995996 (NC_000020.11:35310644::AA 12467/42334) Row 550995997 (NC_000020.11:35310644::AAA 601/42062)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 550995995 (NC_000020.11:35310644::A 1477/41278) Row 550995996 (NC_000020.11:35310644::AA 12467/42334) Row 550995997 (NC_000020.11:35310644::AAA 601/42062)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 550995995 (NC_000020.11:35310644::A 1477/41278) Row 550995996 (NC_000020.11:35310644::AA 12467/42334) Row 550995997 (NC_000020.11:35310644::AAA 601/42062)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 550995995 (NC_000020.11:35310644::A 1477/41278) Row 550995996 (NC_000020.11:35310644::AA 12467/42334) Row 550995997 (NC_000020.11:35310644::AAA 601/42062)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 550995995 (NC_000020.11:35310644::A 1477/41278) Row 550995996 (NC_000020.11:35310644::AA 12467/42334) Row 550995997 (NC_000020.11:35310644::AAA 601/42062)...	-	Apr 27, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 550995995 (NC_000020.11:35310644::A 1477/41278) Row 550995996 (NC_000020.11:35310644::AA 12467/42334) Row 550995997 (NC_000020.11:35310644::AAA 601/42062)...	-	Apr 27, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 550995995 (NC_000020.11:35310644::A 1477/41278) Row 550995996 (NC_000020.11:35310644::AA 12467/42334) Row 550995997 (NC_000020.11:35310644::AAA 601/42062)...	-	Apr 27, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 550995995 (NC_000020.11:35310644::A 1477/41278) Row 550995996 (NC_000020.11:35310644::AA 12467/42334) Row 550995997 (NC_000020.11:35310644::AAA 601/42062)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 550995995 (NC_000020.11:35310644::A 1477/41278) Row 550995996 (NC_000020.11:35310644::AA 12467/42334) Row 550995997 (NC_000020.11:35310644::AAA 601/42062)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 550995995 (NC_000020.11:35310644::A 1477/41278) Row 550995996 (NC_000020.11:35310644::AA 12467/42334) Row 550995997 (NC_000020.11:35310644::AAA 601/42062)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 550995995 (NC_000020.11:35310644::A 1477/41278) Row 550995996 (NC_000020.11:35310644::AA 12467/42334) Row 550995997 (NC_000020.11:35310644::AAA 601/42062)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 550995995 (NC_000020.11:35310644::A 1477/41278) Row 550995996 (NC_000020.11:35310644::AA 12467/42334) Row 550995997 (NC_000020.11:35310644::AAA 601/42062)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 550995995 (NC_000020.11:35310644::A 1477/41278) Row 550995996 (NC_000020.11:35310644::AA 12467/42334) Row 550995997 (NC_000020.11:35310644::AAA 601/42062)...	-	Apr 27, 2021 (155)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 38598165 (NC_000020.11:35310646::A 158/1562) Row 38598166 (NC_000020.11:35310644:AA: 41/1562) Row 38598167 (NC_000020.11:35310645:A: 266/1562)...	-	Apr 27, 2020 (154)
61	Korean Genome Project Submission ignored due to conflicting rows: Row 38598165 (NC_000020.11:35310646::A 158/1562) Row 38598166 (NC_000020.11:35310644:AA: 41/1562) Row 38598167 (NC_000020.11:35310645:A: 266/1562)...	-	Apr 27, 2020 (154)
62	Korean Genome Project Submission ignored due to conflicting rows: Row 38598165 (NC_000020.11:35310646::A 158/1562) Row 38598166 (NC_000020.11:35310644:AA: 41/1562) Row 38598167 (NC_000020.11:35310645:A: 266/1562)...	-	Apr 27, 2020 (154)
63	Korean Genome Project Submission ignored due to conflicting rows: Row 38598165 (NC_000020.11:35310646::A 158/1562) Row 38598166 (NC_000020.11:35310644:AA: 41/1562) Row 38598167 (NC_000020.11:35310645:A: 266/1562)...	-	Apr 27, 2020 (154)
64	Korean Genome Project Submission ignored due to conflicting rows: Row 38598165 (NC_000020.11:35310646::A 158/1562) Row 38598166 (NC_000020.11:35310644:AA: 41/1562) Row 38598167 (NC_000020.11:35310645:A: 266/1562)...	-	Apr 27, 2020 (154)
65	8.3KJPN Submission ignored due to conflicting rows: Row 87480331 (NC_000020.10:33898447:A: 1799/16012) Row 87480332 (NC_000020.10:33898447::AA 878/16012) Row 87480333 (NC_000020.10:33898447::A 322/16012)...	-	Apr 27, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 87480331 (NC_000020.10:33898447:A: 1799/16012) Row 87480332 (NC_000020.10:33898447::AA 878/16012) Row 87480333 (NC_000020.10:33898447::A 322/16012)...	-	Apr 27, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 87480331 (NC_000020.10:33898447:A: 1799/16012) Row 87480332 (NC_000020.10:33898447::AA 878/16012) Row 87480333 (NC_000020.10:33898447::A 322/16012)...	-	Apr 27, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 87480331 (NC_000020.10:33898447:A: 1799/16012) Row 87480332 (NC_000020.10:33898447::AA 878/16012) Row 87480333 (NC_000020.10:33898447::A 322/16012)...	-	Apr 27, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 87480331 (NC_000020.10:33898447:A: 1799/16012) Row 87480332 (NC_000020.10:33898447::AA 878/16012) Row 87480333 (NC_000020.10:33898447::A 322/16012)...	-	Apr 27, 2021 (155)
70	14KJPN Submission ignored due to conflicting rows: Row 123105659 (NC_000020.11:35310644:A: 3206/27210) Row 123105660 (NC_000020.11:35310644::AA 1370/27210) Row 123105661 (NC_000020.11:35310644::A 412/27210)...	-	Oct 16, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 123105659 (NC_000020.11:35310644:A: 3206/27210) Row 123105660 (NC_000020.11:35310644::AA 1370/27210) Row 123105661 (NC_000020.11:35310644::A 412/27210)...	-	Oct 16, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 123105659 (NC_000020.11:35310644:A: 3206/27210) Row 123105660 (NC_000020.11:35310644::AA 1370/27210) Row 123105661 (NC_000020.11:35310644::A 412/27210)...	-	Oct 16, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 123105659 (NC_000020.11:35310644:A: 3206/27210) Row 123105660 (NC_000020.11:35310644::AA 1370/27210) Row 123105661 (NC_000020.11:35310644::A 412/27210)...	-	Oct 16, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 123105659 (NC_000020.11:35310644:A: 3206/27210) Row 123105660 (NC_000020.11:35310644::AA 1370/27210) Row 123105661 (NC_000020.11:35310644::A 412/27210)...	-	Oct 16, 2022 (156)
75	ALFA	NC_000020.11 - 35310645	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4352883245	NC_000020.11:35310644:AAAAAAAAAAA:	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
2427037948	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
2427037948	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4352883244	NC_000020.11:35310644:AAAAAAA:	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
2427037948	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4352883243	NC_000020.11:35310644:AAAAAA:	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
2427037948	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4352883242	NC_000020.11:35310644:AAAAA:	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
2427037948	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4352883241	NC_000020.11:35310644:AAAA:	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
2427037948	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4352883240	NC_000020.11:35310644:AAA:	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
2427037948	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3018137901, ss5229511028	NC_000020.10:33898447:AA:	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3706888177, ss3982220165, ss4352883239, ss5789268559	NC_000020.11:35310644:AA:	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
2427037948	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5229511024	NC_000020.10:33898447:A:	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5789268555	NC_000020.11:35310644:A:	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
2427037948	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3706888176, ss3982220166	NC_000020.11:35310645:A:	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3793534105, ss3798421004, ss5229511026	NC_000020.10:33898447::A	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4352883231, ss5789268557	NC_000020.11:35310644::A	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2427037948	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3706888175, ss3982220164	NC_000020.11:35310646::A	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3793534106, ss3798421005, ss5229511025	NC_000020.10:33898447::AA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3064854609, ss4352883232, ss5789268556	NC_000020.11:35310644::AA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2427037948	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3706888174, ss3982220167	NC_000020.11:35310646::AA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3835658811, ss5229511027	NC_000020.10:33898447::AAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4352883233, ss5789268558	NC_000020.11:35310644::AAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2427037948	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3706888173, ss3982220168	NC_000020.11:35310646::AAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4352883234	NC_000020.11:35310644::AAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2427037948	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4352883235	NC_000020.11:35310644::AAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2427037948	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4352883236	NC_000020.11:35310644::AAAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2427037948	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4352883237	NC_000020.11:35310644::AAAAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4352883238	NC_000020.11:35310644::AAAAAAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2427037948	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3706888172	NC_000020.11:35310646::AAAAAAAAA	NC_000020.11:35310644:AAAAAAAAAAAA… NC_000020.11:35310644:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs1199768843

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

rs1199768843