Name: rs60975859
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.

rs60975859

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:36611494-36611515 (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)₁₄ / del(A)₁₃ / del(A)₁₂ / d…
del(A)₁₄ / del(A)₁₃ / del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₉ / del(A)₈ / 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 / dup(A)₁₃
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₄=0.00000 (0/12110, ALFA)
del(A)₁₃=0.00000 (0/12110, ALFA)
del(A)₁₂=0.00000 (0/12110, ALFA) (+ 17 more)
del(A)₁₁=0.00000 (0/12110, ALFA)
del(A)₁₀=0.00000 (0/12110, ALFA)
del(A)₉=0.00000 (0/12110, ALFA)
del(A)₇=0.00000 (0/12110, ALFA)
del(A)₆=0.00000 (0/12110, ALFA)
del(A)₅=0.00000 (0/12110, ALFA)
del(A)₄=0.00000 (0/12110, ALFA)
delAAA=0.00000 (0/12110, ALFA)
delAA=0.00000 (0/12110, ALFA)
delA=0.00000 (0/12110, ALFA)
dupA=0.00000 (0/12110, ALFA)
dupAA=0.00000 (0/12110, ALFA)
dupAAA=0.00000 (0/12110, ALFA)
dup(A)₄=0.00000 (0/12110, ALFA)
dup(A)₅=0.00000 (0/12110, ALFA)
dup(A)₆=0.00000 (0/12110, ALFA)
dup(A)₇=0.00000 (0/12110, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RAB5IF : Intron Variant
TGIF2-RAB5IF : 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	12110	AAAAAAAAAAAAAAAAAAAAAA=1.00000	AAAAAAAA=0.00000, AAAAAAAAA=0.00000, AAAAAAAAAA=0.00000, AAAAAAAAAAA=0.00000, AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00000	1.0	N/A
European	Sub	8892	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	1914	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	78	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	1836	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	88	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	64	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	24	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	134	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Latin American 2	Sub	572	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	88	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	422	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	12110	(A)₂₂=1.00000	del(A)₁₄=0.00000, del(A)₁₃=0.00000, del(A)₁₂=0.00000, del(A)₁₁=0.00000, del(A)₁₀=0.00000, del(A)₉=0.00000, del(A)₇=0.00000, del(A)₆=0.00000, del(A)₅=0.00000, del(A)₄=0.00000, delAAA=0.00000, delAA=0.00000, delA=0.00000, dupA=0.00000, dupAA=0.00000, dupAAA=0.00000, dup(A)₄=0.00000, dup(A)₅=0.00000, dup(A)₆=0.00000, dup(A)₇=0.00000
Allele Frequency Aggregator	European	Sub	8892	(A)₂₂=1.0000	del(A)₁₄=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₉=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)₇=0.0000
Allele Frequency Aggregator	African	Sub	1914	(A)₂₂=1.0000	del(A)₁₄=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₉=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)₇=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	572	(A)₂₂=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=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)₇=0.000
Allele Frequency Aggregator	Other	Sub	422	(A)₂₂=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=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)₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	134	(A)₂₂=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=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)₇=0.000
Allele Frequency Aggregator	South Asian	Sub	88	(A)₂₂=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=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)₇=0.00
Allele Frequency Aggregator	Asian	Sub	88	(A)₂₂=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=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)₇=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.36611502_36611515del
GRCh38.p14 chr 20	NC_000020.11:g.36611503_36611515del
GRCh38.p14 chr 20	NC_000020.11:g.36611504_36611515del
GRCh38.p14 chr 20	NC_000020.11:g.36611505_36611515del
GRCh38.p14 chr 20	NC_000020.11:g.36611506_36611515del
GRCh38.p14 chr 20	NC_000020.11:g.36611507_36611515del
GRCh38.p14 chr 20	NC_000020.11:g.36611508_36611515del
GRCh38.p14 chr 20	NC_000020.11:g.36611509_36611515del
GRCh38.p14 chr 20	NC_000020.11:g.36611510_36611515del
GRCh38.p14 chr 20	NC_000020.11:g.36611511_36611515del
GRCh38.p14 chr 20	NC_000020.11:g.36611512_36611515del
GRCh38.p14 chr 20	NC_000020.11:g.36611513_36611515del
GRCh38.p14 chr 20	NC_000020.11:g.36611514_36611515del
GRCh38.p14 chr 20	NC_000020.11:g.36611515del
GRCh38.p14 chr 20	NC_000020.11:g.36611515dup
GRCh38.p14 chr 20	NC_000020.11:g.36611514_36611515dup
GRCh38.p14 chr 20	NC_000020.11:g.36611513_36611515dup
GRCh38.p14 chr 20	NC_000020.11:g.36611512_36611515dup
GRCh38.p14 chr 20	NC_000020.11:g.36611511_36611515dup
GRCh38.p14 chr 20	NC_000020.11:g.36611510_36611515dup
GRCh38.p14 chr 20	NC_000020.11:g.36611509_36611515dup
GRCh38.p14 chr 20	NC_000020.11:g.36611507_36611515dup
GRCh38.p14 chr 20	NC_000020.11:g.36611503_36611515dup
GRCh37.p13 chr 20	NC_000020.10:g.35239905_35239918del
GRCh37.p13 chr 20	NC_000020.10:g.35239906_35239918del
GRCh37.p13 chr 20	NC_000020.10:g.35239907_35239918del
GRCh37.p13 chr 20	NC_000020.10:g.35239908_35239918del
GRCh37.p13 chr 20	NC_000020.10:g.35239909_35239918del
GRCh37.p13 chr 20	NC_000020.10:g.35239910_35239918del
GRCh37.p13 chr 20	NC_000020.10:g.35239911_35239918del
GRCh37.p13 chr 20	NC_000020.10:g.35239912_35239918del
GRCh37.p13 chr 20	NC_000020.10:g.35239913_35239918del
GRCh37.p13 chr 20	NC_000020.10:g.35239914_35239918del
GRCh37.p13 chr 20	NC_000020.10:g.35239915_35239918del
GRCh37.p13 chr 20	NC_000020.10:g.35239916_35239918del
GRCh37.p13 chr 20	NC_000020.10:g.35239917_35239918del
GRCh37.p13 chr 20	NC_000020.10:g.35239918del
GRCh37.p13 chr 20	NC_000020.10:g.35239918dup
GRCh37.p13 chr 20	NC_000020.10:g.35239917_35239918dup
GRCh37.p13 chr 20	NC_000020.10:g.35239916_35239918dup
GRCh37.p13 chr 20	NC_000020.10:g.35239915_35239918dup
GRCh37.p13 chr 20	NC_000020.10:g.35239914_35239918dup
GRCh37.p13 chr 20	NC_000020.10:g.35239913_35239918dup
GRCh37.p13 chr 20	NC_000020.10:g.35239912_35239918dup
GRCh37.p13 chr 20	NC_000020.10:g.35239910_35239918dup
GRCh37.p13 chr 20	NC_000020.10:g.35239906_35239918dup
SLA2 RefSeqGene	NG_031823.2:g.39710_39723del
SLA2 RefSeqGene	NG_031823.2:g.39711_39723del
SLA2 RefSeqGene	NG_031823.2:g.39712_39723del
SLA2 RefSeqGene	NG_031823.2:g.39713_39723del
SLA2 RefSeqGene	NG_031823.2:g.39714_39723del
SLA2 RefSeqGene	NG_031823.2:g.39715_39723del
SLA2 RefSeqGene	NG_031823.2:g.39716_39723del
SLA2 RefSeqGene	NG_031823.2:g.39717_39723del
SLA2 RefSeqGene	NG_031823.2:g.39718_39723del
SLA2 RefSeqGene	NG_031823.2:g.39719_39723del
SLA2 RefSeqGene	NG_031823.2:g.39720_39723del
SLA2 RefSeqGene	NG_031823.2:g.39721_39723del
SLA2 RefSeqGene	NG_031823.2:g.39722_39723del
SLA2 RefSeqGene	NG_031823.2:g.39723del
SLA2 RefSeqGene	NG_031823.2:g.39723dup
SLA2 RefSeqGene	NG_031823.2:g.39722_39723dup
SLA2 RefSeqGene	NG_031823.2:g.39721_39723dup
SLA2 RefSeqGene	NG_031823.2:g.39720_39723dup
SLA2 RefSeqGene	NG_031823.2:g.39719_39723dup
SLA2 RefSeqGene	NG_031823.2:g.39718_39723dup
SLA2 RefSeqGene	NG_031823.2:g.39717_39723dup
SLA2 RefSeqGene	NG_031823.2:g.39715_39723dup
SLA2 RefSeqGene	NG_031823.2:g.39711_39723dup

Gene: RAB5IF, RAB5 interacting factor (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RAB5IF transcript variant 4	NM_001199534.2:c.377-508_… NM_001199534.2:c.377-508_377-495del	N/A	Intron Variant
RAB5IF transcript variant 5	NM_001374178.1:c.349-490_… NM_001374178.1:c.349-490_349-477del	N/A	Intron Variant
RAB5IF transcript variant 1	NM_018840.5:c.349-508_349… NM_018840.5:c.349-508_349-495del	N/A	Intron Variant
RAB5IF transcript variant 2	NM_199483.3:c.219-508_219… NM_199483.3:c.219-508_219-495del	N/A	Intron Variant
RAB5IF transcript variant 3	NR_026562.4:n.	N/A	Intron Variant
RAB5IF transcript variant 6	NR_164350.1:n.	N/A	Intron Variant
RAB5IF transcript variant 7	NR_164351.1:n.	N/A	Intron Variant

Gene: TGIF2-RAB5IF, TGIF2-RAB5IF readthrough (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TGIF2-RAB5IF transcript	NM_001199535.2:c.427-508_… NM_001199535.2:c.427-508_427-495del	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)₂₂=	del(A)₁₄	del(A)₁₃	del(A)₁₂	del(A)₁₁	del(A)₁₀	del(A)₉	del(A)₈	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	dup(A)₁₃
GRCh38.p14 chr 20	NC_000020.11:g.36611494_36611515=	NC_000020.11:g.36611502_36611515del	NC_000020.11:g.36611503_36611515del	NC_000020.11:g.36611504_36611515del	NC_000020.11:g.36611505_36611515del	NC_000020.11:g.36611506_36611515del	NC_000020.11:g.36611507_36611515del	NC_000020.11:g.36611508_36611515del	NC_000020.11:g.36611509_36611515del	NC_000020.11:g.36611510_36611515del	NC_000020.11:g.36611511_36611515del	NC_000020.11:g.36611512_36611515del	NC_000020.11:g.36611513_36611515del	NC_000020.11:g.36611514_36611515del	NC_000020.11:g.36611515del	NC_000020.11:g.36611515dup	NC_000020.11:g.36611514_36611515dup	NC_000020.11:g.36611513_36611515dup	NC_000020.11:g.36611512_36611515dup	NC_000020.11:g.36611511_36611515dup	NC_000020.11:g.36611510_36611515dup	NC_000020.11:g.36611509_36611515dup	NC_000020.11:g.36611507_36611515dup	NC_000020.11:g.36611503_36611515dup
GRCh37.p13 chr 20	NC_000020.10:g.35239897_35239918=	NC_000020.10:g.35239905_35239918del	NC_000020.10:g.35239906_35239918del	NC_000020.10:g.35239907_35239918del	NC_000020.10:g.35239908_35239918del	NC_000020.10:g.35239909_35239918del	NC_000020.10:g.35239910_35239918del	NC_000020.10:g.35239911_35239918del	NC_000020.10:g.35239912_35239918del	NC_000020.10:g.35239913_35239918del	NC_000020.10:g.35239914_35239918del	NC_000020.10:g.35239915_35239918del	NC_000020.10:g.35239916_35239918del	NC_000020.10:g.35239917_35239918del	NC_000020.10:g.35239918del	NC_000020.10:g.35239918dup	NC_000020.10:g.35239917_35239918dup	NC_000020.10:g.35239916_35239918dup	NC_000020.10:g.35239915_35239918dup	NC_000020.10:g.35239914_35239918dup	NC_000020.10:g.35239913_35239918dup	NC_000020.10:g.35239912_35239918dup	NC_000020.10:g.35239910_35239918dup	NC_000020.10:g.35239906_35239918dup
SLA2 RefSeqGene	NG_031823.2:g.39702_39723=	NG_031823.2:g.39710_39723del	NG_031823.2:g.39711_39723del	NG_031823.2:g.39712_39723del	NG_031823.2:g.39713_39723del	NG_031823.2:g.39714_39723del	NG_031823.2:g.39715_39723del	NG_031823.2:g.39716_39723del	NG_031823.2:g.39717_39723del	NG_031823.2:g.39718_39723del	NG_031823.2:g.39719_39723del	NG_031823.2:g.39720_39723del	NG_031823.2:g.39721_39723del	NG_031823.2:g.39722_39723del	NG_031823.2:g.39723del	NG_031823.2:g.39723dup	NG_031823.2:g.39722_39723dup	NG_031823.2:g.39721_39723dup	NG_031823.2:g.39720_39723dup	NG_031823.2:g.39719_39723dup	NG_031823.2:g.39718_39723dup	NG_031823.2:g.39717_39723dup	NG_031823.2:g.39715_39723dup	NG_031823.2:g.39711_39723dup
RAB5IF transcript variant 4	NM_001199534.1:c.377-516=	NM_001199534.1:c.377-508_377-495del	NM_001199534.1:c.377-507_377-495del	NM_001199534.1:c.377-506_377-495del	NM_001199534.1:c.377-505_377-495del	NM_001199534.1:c.377-504_377-495del	NM_001199534.1:c.377-503_377-495del	NM_001199534.1:c.377-502_377-495del	NM_001199534.1:c.377-501_377-495del	NM_001199534.1:c.377-500_377-495del	NM_001199534.1:c.377-499_377-495del	NM_001199534.1:c.377-498_377-495del	NM_001199534.1:c.377-497_377-495del	NM_001199534.1:c.377-496_377-495del	NM_001199534.1:c.377-495del	NM_001199534.1:c.377-495dup	NM_001199534.1:c.377-496_377-495dup	NM_001199534.1:c.377-497_377-495dup	NM_001199534.1:c.377-498_377-495dup	NM_001199534.1:c.377-499_377-495dup	NM_001199534.1:c.377-500_377-495dup	NM_001199534.1:c.377-501_377-495dup	NM_001199534.1:c.377-503_377-495dup	NM_001199534.1:c.377-507_377-495dup
RAB5IF transcript variant 4	NM_001199534.2:c.377-516=	NM_001199534.2:c.377-508_377-495del	NM_001199534.2:c.377-507_377-495del	NM_001199534.2:c.377-506_377-495del	NM_001199534.2:c.377-505_377-495del	NM_001199534.2:c.377-504_377-495del	NM_001199534.2:c.377-503_377-495del	NM_001199534.2:c.377-502_377-495del	NM_001199534.2:c.377-501_377-495del	NM_001199534.2:c.377-500_377-495del	NM_001199534.2:c.377-499_377-495del	NM_001199534.2:c.377-498_377-495del	NM_001199534.2:c.377-497_377-495del	NM_001199534.2:c.377-496_377-495del	NM_001199534.2:c.377-495del	NM_001199534.2:c.377-495dup	NM_001199534.2:c.377-496_377-495dup	NM_001199534.2:c.377-497_377-495dup	NM_001199534.2:c.377-498_377-495dup	NM_001199534.2:c.377-499_377-495dup	NM_001199534.2:c.377-500_377-495dup	NM_001199534.2:c.377-501_377-495dup	NM_001199534.2:c.377-503_377-495dup	NM_001199534.2:c.377-507_377-495dup
TGIF2-RAB5IF transcript	NM_001199535.1:c.427-516=	NM_001199535.1:c.427-508_427-495del	NM_001199535.1:c.427-507_427-495del	NM_001199535.1:c.427-506_427-495del	NM_001199535.1:c.427-505_427-495del	NM_001199535.1:c.427-504_427-495del	NM_001199535.1:c.427-503_427-495del	NM_001199535.1:c.427-502_427-495del	NM_001199535.1:c.427-501_427-495del	NM_001199535.1:c.427-500_427-495del	NM_001199535.1:c.427-499_427-495del	NM_001199535.1:c.427-498_427-495del	NM_001199535.1:c.427-497_427-495del	NM_001199535.1:c.427-496_427-495del	NM_001199535.1:c.427-495del	NM_001199535.1:c.427-495dup	NM_001199535.1:c.427-496_427-495dup	NM_001199535.1:c.427-497_427-495dup	NM_001199535.1:c.427-498_427-495dup	NM_001199535.1:c.427-499_427-495dup	NM_001199535.1:c.427-500_427-495dup	NM_001199535.1:c.427-501_427-495dup	NM_001199535.1:c.427-503_427-495dup	NM_001199535.1:c.427-507_427-495dup
TGIF2-RAB5IF transcript	NM_001199535.2:c.427-516=	NM_001199535.2:c.427-508_427-495del	NM_001199535.2:c.427-507_427-495del	NM_001199535.2:c.427-506_427-495del	NM_001199535.2:c.427-505_427-495del	NM_001199535.2:c.427-504_427-495del	NM_001199535.2:c.427-503_427-495del	NM_001199535.2:c.427-502_427-495del	NM_001199535.2:c.427-501_427-495del	NM_001199535.2:c.427-500_427-495del	NM_001199535.2:c.427-499_427-495del	NM_001199535.2:c.427-498_427-495del	NM_001199535.2:c.427-497_427-495del	NM_001199535.2:c.427-496_427-495del	NM_001199535.2:c.427-495del	NM_001199535.2:c.427-495dup	NM_001199535.2:c.427-496_427-495dup	NM_001199535.2:c.427-497_427-495dup	NM_001199535.2:c.427-498_427-495dup	NM_001199535.2:c.427-499_427-495dup	NM_001199535.2:c.427-500_427-495dup	NM_001199535.2:c.427-501_427-495dup	NM_001199535.2:c.427-503_427-495dup	NM_001199535.2:c.427-507_427-495dup
RAB5IF transcript variant 5	NM_001374178.1:c.349-498=	NM_001374178.1:c.349-490_349-477del	NM_001374178.1:c.349-489_349-477del	NM_001374178.1:c.349-488_349-477del	NM_001374178.1:c.349-487_349-477del	NM_001374178.1:c.349-486_349-477del	NM_001374178.1:c.349-485_349-477del	NM_001374178.1:c.349-484_349-477del	NM_001374178.1:c.349-483_349-477del	NM_001374178.1:c.349-482_349-477del	NM_001374178.1:c.349-481_349-477del	NM_001374178.1:c.349-480_349-477del	NM_001374178.1:c.349-479_349-477del	NM_001374178.1:c.349-478_349-477del	NM_001374178.1:c.349-477del	NM_001374178.1:c.349-477dup	NM_001374178.1:c.349-478_349-477dup	NM_001374178.1:c.349-479_349-477dup	NM_001374178.1:c.349-480_349-477dup	NM_001374178.1:c.349-481_349-477dup	NM_001374178.1:c.349-482_349-477dup	NM_001374178.1:c.349-483_349-477dup	NM_001374178.1:c.349-485_349-477dup	NM_001374178.1:c.349-489_349-477dup
RAB5IF transcript variant 1	NM_018840.4:c.349-516=	NM_018840.4:c.349-508_349-495del	NM_018840.4:c.349-507_349-495del	NM_018840.4:c.349-506_349-495del	NM_018840.4:c.349-505_349-495del	NM_018840.4:c.349-504_349-495del	NM_018840.4:c.349-503_349-495del	NM_018840.4:c.349-502_349-495del	NM_018840.4:c.349-501_349-495del	NM_018840.4:c.349-500_349-495del	NM_018840.4:c.349-499_349-495del	NM_018840.4:c.349-498_349-495del	NM_018840.4:c.349-497_349-495del	NM_018840.4:c.349-496_349-495del	NM_018840.4:c.349-495del	NM_018840.4:c.349-495dup	NM_018840.4:c.349-496_349-495dup	NM_018840.4:c.349-497_349-495dup	NM_018840.4:c.349-498_349-495dup	NM_018840.4:c.349-499_349-495dup	NM_018840.4:c.349-500_349-495dup	NM_018840.4:c.349-501_349-495dup	NM_018840.4:c.349-503_349-495dup	NM_018840.4:c.349-507_349-495dup
RAB5IF transcript variant 1	NM_018840.5:c.349-516=	NM_018840.5:c.349-508_349-495del	NM_018840.5:c.349-507_349-495del	NM_018840.5:c.349-506_349-495del	NM_018840.5:c.349-505_349-495del	NM_018840.5:c.349-504_349-495del	NM_018840.5:c.349-503_349-495del	NM_018840.5:c.349-502_349-495del	NM_018840.5:c.349-501_349-495del	NM_018840.5:c.349-500_349-495del	NM_018840.5:c.349-499_349-495del	NM_018840.5:c.349-498_349-495del	NM_018840.5:c.349-497_349-495del	NM_018840.5:c.349-496_349-495del	NM_018840.5:c.349-495del	NM_018840.5:c.349-495dup	NM_018840.5:c.349-496_349-495dup	NM_018840.5:c.349-497_349-495dup	NM_018840.5:c.349-498_349-495dup	NM_018840.5:c.349-499_349-495dup	NM_018840.5:c.349-500_349-495dup	NM_018840.5:c.349-501_349-495dup	NM_018840.5:c.349-503_349-495dup	NM_018840.5:c.349-507_349-495dup
RAB5IF transcript variant 2	NM_199483.2:c.219-516=	NM_199483.2:c.219-508_219-495del	NM_199483.2:c.219-507_219-495del	NM_199483.2:c.219-506_219-495del	NM_199483.2:c.219-505_219-495del	NM_199483.2:c.219-504_219-495del	NM_199483.2:c.219-503_219-495del	NM_199483.2:c.219-502_219-495del	NM_199483.2:c.219-501_219-495del	NM_199483.2:c.219-500_219-495del	NM_199483.2:c.219-499_219-495del	NM_199483.2:c.219-498_219-495del	NM_199483.2:c.219-497_219-495del	NM_199483.2:c.219-496_219-495del	NM_199483.2:c.219-495del	NM_199483.2:c.219-495dup	NM_199483.2:c.219-496_219-495dup	NM_199483.2:c.219-497_219-495dup	NM_199483.2:c.219-498_219-495dup	NM_199483.2:c.219-499_219-495dup	NM_199483.2:c.219-500_219-495dup	NM_199483.2:c.219-501_219-495dup	NM_199483.2:c.219-503_219-495dup	NM_199483.2:c.219-507_219-495dup
RAB5IF transcript variant 2	NM_199483.3:c.219-516=	NM_199483.3:c.219-508_219-495del	NM_199483.3:c.219-507_219-495del	NM_199483.3:c.219-506_219-495del	NM_199483.3:c.219-505_219-495del	NM_199483.3:c.219-504_219-495del	NM_199483.3:c.219-503_219-495del	NM_199483.3:c.219-502_219-495del	NM_199483.3:c.219-501_219-495del	NM_199483.3:c.219-500_219-495del	NM_199483.3:c.219-499_219-495del	NM_199483.3:c.219-498_219-495del	NM_199483.3:c.219-497_219-495del	NM_199483.3:c.219-496_219-495del	NM_199483.3:c.219-495del	NM_199483.3:c.219-495dup	NM_199483.3:c.219-496_219-495dup	NM_199483.3:c.219-497_219-495dup	NM_199483.3:c.219-498_219-495dup	NM_199483.3:c.219-499_219-495dup	NM_199483.3:c.219-500_219-495dup	NM_199483.3:c.219-501_219-495dup	NM_199483.3:c.219-503_219-495dup	NM_199483.3:c.219-507_219-495dup

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#.

50 SubSNP, 39 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss82219838	Dec 15, 2007 (129)
2	PACBIO	ss3793535105	Jul 13, 2019 (153)
3	PACBIO	ss3798422016	Jul 13, 2019 (153)
4	EVA	ss3835661620	Apr 27, 2020 (154)
5	KOGIC	ss3982238751	Apr 27, 2020 (154)
6	KOGIC	ss3982238752	Apr 27, 2020 (154)
7	KOGIC	ss3982238753	Apr 27, 2020 (154)
8	KOGIC	ss3982238754	Apr 27, 2020 (154)
9	KOGIC	ss3982238755	Apr 27, 2020 (154)
10	KOGIC	ss3982238756	Apr 27, 2020 (154)
11	GNOMAD	ss4353046427	Apr 26, 2021 (155)
12	GNOMAD	ss4353046428	Apr 26, 2021 (155)
13	GNOMAD	ss4353046429	Apr 26, 2021 (155)
14	GNOMAD	ss4353046430	Apr 26, 2021 (155)
15	GNOMAD	ss4353046431	Apr 26, 2021 (155)
16	GNOMAD	ss4353046432	Apr 26, 2021 (155)
17	GNOMAD	ss4353046433	Apr 26, 2021 (155)
18	GNOMAD	ss4353046434	Apr 26, 2021 (155)
19	GNOMAD	ss4353046435	Apr 26, 2021 (155)
20	GNOMAD	ss4353046437	Apr 26, 2021 (155)
21	GNOMAD	ss4353046438	Apr 26, 2021 (155)
22	GNOMAD	ss4353046439	Apr 26, 2021 (155)
23	GNOMAD	ss4353046440	Apr 26, 2021 (155)
24	GNOMAD	ss4353046441	Apr 26, 2021 (155)
25	GNOMAD	ss4353046442	Apr 26, 2021 (155)
26	GNOMAD	ss4353046443	Apr 26, 2021 (155)
27	GNOMAD	ss4353046444	Apr 26, 2021 (155)
28	GNOMAD	ss4353046445	Apr 26, 2021 (155)
29	GNOMAD	ss4353046446	Apr 26, 2021 (155)
30	GNOMAD	ss4353046447	Apr 26, 2021 (155)
31	GNOMAD	ss4353046448	Apr 26, 2021 (155)
32	GNOMAD	ss4353046449	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5229553018	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5229553019	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5229553020	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5229553021	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5229553022	Apr 26, 2021 (155)
38	1000G_HIGH_COVERAGE	ss5308725006	Oct 16, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5308725007	Oct 16, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5308725008	Oct 16, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5308725009	Oct 16, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5308725010	Oct 16, 2022 (156)
43	HUGCELL_USP	ss5501009292	Oct 16, 2022 (156)
44	HUGCELL_USP	ss5501009293	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5501009294	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5501009295	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5789325683	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5789325684	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5789325685	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5789325687	Oct 16, 2022 (156)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551255483 (NC_000020.11:36611493::A 4024/41182) Row 551255484 (NC_000020.11:36611493::AA 135/42602) Row 551255485 (NC_000020.11:36611493::AAA 321/42806)...	-	Apr 26, 2021 (155)
74	Korean Genome Project Submission ignored due to conflicting rows: Row 38616752 (NC_000020.11:36611497::AA 47/1674) Row 38616753 (NC_000020.11:36611495:AA: 90/1674) Row 38616754 (NC_000020.11:36611497::A 274/1674)...	-	Apr 27, 2020 (154)
75	Korean Genome Project Submission ignored due to conflicting rows: Row 38616752 (NC_000020.11:36611497::AA 47/1674) Row 38616753 (NC_000020.11:36611495:AA: 90/1674) Row 38616754 (NC_000020.11:36611497::A 274/1674)...	-	Apr 27, 2020 (154)
76	Korean Genome Project Submission ignored due to conflicting rows: Row 38616752 (NC_000020.11:36611497::AA 47/1674) Row 38616753 (NC_000020.11:36611495:AA: 90/1674) Row 38616754 (NC_000020.11:36611497::A 274/1674)...	-	Apr 27, 2020 (154)
77	Korean Genome Project Submission ignored due to conflicting rows: Row 38616752 (NC_000020.11:36611497::AA 47/1674) Row 38616753 (NC_000020.11:36611495:AA: 90/1674) Row 38616754 (NC_000020.11:36611497::A 274/1674)...	-	Apr 27, 2020 (154)
78	Korean Genome Project Submission ignored due to conflicting rows: Row 38616752 (NC_000020.11:36611497::AA 47/1674) Row 38616753 (NC_000020.11:36611495:AA: 90/1674) Row 38616754 (NC_000020.11:36611497::A 274/1674)...	-	Apr 27, 2020 (154)
79	Korean Genome Project Submission ignored due to conflicting rows: Row 38616752 (NC_000020.11:36611497::AA 47/1674) Row 38616753 (NC_000020.11:36611495:AA: 90/1674) Row 38616754 (NC_000020.11:36611497::A 274/1674)...	-	Apr 27, 2020 (154)
80	8.3KJPN Submission ignored due to conflicting rows: Row 87522325 (NC_000020.10:35239896::A 996/16512) Row 87522326 (NC_000020.10:35239896:AA: 522/16512) Row 87522327 (NC_000020.10:35239896:AAAA: 36/16512)...	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 87522325 (NC_000020.10:35239896::A 996/16512) Row 87522326 (NC_000020.10:35239896:AA: 522/16512) Row 87522327 (NC_000020.10:35239896:AAAA: 36/16512)...	-	Apr 26, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 87522325 (NC_000020.10:35239896::A 996/16512) Row 87522326 (NC_000020.10:35239896:AA: 522/16512) Row 87522327 (NC_000020.10:35239896:AAAA: 36/16512)...	-	Apr 26, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 87522325 (NC_000020.10:35239896::A 996/16512) Row 87522326 (NC_000020.10:35239896:AA: 522/16512) Row 87522327 (NC_000020.10:35239896:AAAA: 36/16512)...	-	Apr 26, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 87522325 (NC_000020.10:35239896::A 996/16512) Row 87522326 (NC_000020.10:35239896:AA: 522/16512) Row 87522327 (NC_000020.10:35239896:AAAA: 36/16512)...	-	Apr 26, 2021 (155)
85	14KJPN Submission ignored due to conflicting rows: Row 123162787 (NC_000020.11:36611493::A 1929/28176) Row 123162788 (NC_000020.11:36611493:AA: 1058/28176) Row 123162789 (NC_000020.11:36611493:AAAA: 62/28176)...	-	Oct 16, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 123162787 (NC_000020.11:36611493::A 1929/28176) Row 123162788 (NC_000020.11:36611493:AA: 1058/28176) Row 123162789 (NC_000020.11:36611493:AAAA: 62/28176)...	-	Oct 16, 2022 (156)
87	14KJPN Submission ignored due to conflicting rows: Row 123162787 (NC_000020.11:36611493::A 1929/28176) Row 123162788 (NC_000020.11:36611493:AA: 1058/28176) Row 123162789 (NC_000020.11:36611493:AAAA: 62/28176)...	-	Oct 16, 2022 (156)
88	14KJPN Submission ignored due to conflicting rows: Row 123162787 (NC_000020.11:36611493::A 1929/28176) Row 123162788 (NC_000020.11:36611493:AA: 1058/28176) Row 123162789 (NC_000020.11:36611493:AAAA: 62/28176)...	-	Oct 16, 2022 (156)
89	ALFA	NC_000020.11 - 36611494	Apr 26, 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
ss4353046449	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
11436779380	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
ss4353046448	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
11436779380	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4353046447	NC_000020.11:36611493:AAAAAAAAAAAA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
11436779380	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4353046446	NC_000020.11:36611493:AAAAAAAAAAA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
11436779380	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4353046445	NC_000020.11:36611493:AAAAAAAAAA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
11436779380	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss82219838	NC_000020.9:34673323:AAAAAAAAA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4353046444	NC_000020.11:36611493:AAAAAAAAA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
11436779380	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4353046443	NC_000020.11:36611493:AAAAAAAA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4353046442	NC_000020.11:36611493:AAAAAAA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
11436779380	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4353046441	NC_000020.11:36611493:AAAAAA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
11436779380	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4353046440	NC_000020.11:36611493:AAAAA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
11436779380	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5229553020	NC_000020.10:35239896:AAAA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3982238756, ss4353046439, ss5789325685	NC_000020.11:36611493:AAAA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
11436779380	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4353046438	NC_000020.11:36611493:AAA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
11436779380	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3982238755	NC_000020.11:36611494:AAA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5229553019	NC_000020.10:35239896:AA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4353046437, ss5308725010, ss5789325684	NC_000020.11:36611493:AA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
11436779380	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3982238752	NC_000020.11:36611495:AA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3793535105, ss3798422016, ss5229553021	NC_000020.10:35239896:A:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5308725007, ss5501009293	NC_000020.11:36611493:A:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
11436779380	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3982238754	NC_000020.11:36611496:A:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5229553018	NC_000020.10:35239896::A	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4353046427, ss5308725006, ss5501009292, ss5789325683	NC_000020.11:36611493::A	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
11436779380	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3982238753	NC_000020.11:36611497::A	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3835661620, ss5229553022	NC_000020.10:35239896::AA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4353046428, ss5501009294, ss5789325687	NC_000020.11:36611493::AA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
11436779380	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3982238751	NC_000020.11:36611497::AA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4353046429, ss5308725009, ss5501009295	NC_000020.11:36611493::AAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
11436779380	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4353046430, ss5308725008	NC_000020.11:36611493::AAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
11436779380	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4353046431	NC_000020.11:36611493::AAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
11436779380	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4353046432	NC_000020.11:36611493::AAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
11436779380	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4353046433	NC_000020.11:36611493::AAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
11436779380	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4353046434	NC_000020.11:36611493::AAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4353046435	NC_000020.11:36611493::AAAAAAAAAAA… NC_000020.11:36611493::AAAAAAAAAAAAA	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI
ss2409103821	NC_000020.10:35239896:AAAAAAAAAA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA
ss2409103822	NC_000020.10:35239896:AAAAAAAAAAAA… NC_000020.10:35239896:AAAAAAAAAAAAA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA
ss2409103823	NC_000020.10:35239896:AAAAAAAAAAAA… NC_000020.10:35239896:AAAAAAAAAAAAAA:	NC_000020.11:36611493:AAAAAAAAAAAA… NC_000020.11:36611493:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA

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

No publications for rs60975859

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

rs60975859