Name: rs60124992
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.

rs60124992

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:88661006-88661031 (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)₁₃ / del(A)₁₂ / del(A)₁₁ / d…
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)₈ / dup(A)₉
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₁=0.3383 (1694/5008, 1000G)
del(A)₁₃=0.0000 (0/1654, ALFA)
del(A)₁₂=0.0000 (0/1654, ALFA) (+ 18 more)
del(A)₁₁=0.0000 (0/1654, ALFA)
del(A)₁₀=0.0000 (0/1654, ALFA)
del(A)₉=0.0000 (0/1654, ALFA)
del(A)₈=0.0000 (0/1654, ALFA)
del(A)₇=0.0000 (0/1654, ALFA)
del(A)₆=0.0000 (0/1654, ALFA)
del(A)₅=0.0000 (0/1654, ALFA)
del(A)₄=0.0000 (0/1654, ALFA)
delAAA=0.0000 (0/1654, ALFA)
delAA=0.0000 (0/1654, ALFA)
delA=0.0000 (0/1654, ALFA)
dupA=0.0000 (0/1654, ALFA)
dupAA=0.0000 (0/1654, ALFA)
dupAAA=0.0000 (0/1654, ALFA)
dup(A)₄=0.0000 (0/1654, ALFA)
dup(A)₅=0.0000 (0/1654, ALFA)
dup(A)₆=0.0000 (0/1654, ALFA)
dup(A)₇=0.0000 (0/1654, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MVD : 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	1654	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	936	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African	Sub	436	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	16	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	420	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	38	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	28	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	10	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	26	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	132	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	14	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	72	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	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
1000Genomes	Global	Study-wide	5008	(A)₂₆=0.6617	del(A)₁₁=0.3383
1000Genomes	African	Sub	1322	(A)₂₆=0.4811	del(A)₁₁=0.5189
1000Genomes	East Asian	Sub	1008	(A)₂₆=0.8214	del(A)₁₁=0.1786
1000Genomes	Europe	Sub	1006	(A)₂₆=0.7465	del(A)₁₁=0.2535
1000Genomes	South Asian	Sub	978	(A)₂₆=0.688	del(A)₁₁=0.312
1000Genomes	American	Sub	694	(A)₂₆=0.614	del(A)₁₁=0.386
Allele Frequency Aggregator	Total	Global	1654	(A)₂₆=1.0000	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)₈=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	European	Sub	936	(A)₂₆=1.000	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)₈=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	African	Sub	436	(A)₂₆=1.000	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)₈=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 2	Sub	132	(A)₂₆=1.000	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)₈=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	72	(A)₂₆=1.00	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)₈=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	38	(A)₂₆=1.00	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)₈=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	Latin American 1	Sub	26	(A)₂₆=1.00	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)₈=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	South Asian	Sub	14	(A)₂₆=1.00	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)₈=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 16	NC_000016.10:g.88661019_88661031del
GRCh38.p14 chr 16	NC_000016.10:g.88661020_88661031del
GRCh38.p14 chr 16	NC_000016.10:g.88661021_88661031del
GRCh38.p14 chr 16	NC_000016.10:g.88661022_88661031del
GRCh38.p14 chr 16	NC_000016.10:g.88661023_88661031del
GRCh38.p14 chr 16	NC_000016.10:g.88661024_88661031del
GRCh38.p14 chr 16	NC_000016.10:g.88661025_88661031del
GRCh38.p14 chr 16	NC_000016.10:g.88661026_88661031del
GRCh38.p14 chr 16	NC_000016.10:g.88661027_88661031del
GRCh38.p14 chr 16	NC_000016.10:g.88661028_88661031del
GRCh38.p14 chr 16	NC_000016.10:g.88661029_88661031del
GRCh38.p14 chr 16	NC_000016.10:g.88661030_88661031del
GRCh38.p14 chr 16	NC_000016.10:g.88661031del
GRCh38.p14 chr 16	NC_000016.10:g.88661031dup
GRCh38.p14 chr 16	NC_000016.10:g.88661030_88661031dup
GRCh38.p14 chr 16	NC_000016.10:g.88661029_88661031dup
GRCh38.p14 chr 16	NC_000016.10:g.88661028_88661031dup
GRCh38.p14 chr 16	NC_000016.10:g.88661027_88661031dup
GRCh38.p14 chr 16	NC_000016.10:g.88661026_88661031dup
GRCh38.p14 chr 16	NC_000016.10:g.88661025_88661031dup
GRCh38.p14 chr 16	NC_000016.10:g.88661024_88661031dup
GRCh38.p14 chr 16	NC_000016.10:g.88661023_88661031dup
GRCh37.p13 chr 16	NC_000016.9:g.88727427_88727439del
GRCh37.p13 chr 16	NC_000016.9:g.88727428_88727439del
GRCh37.p13 chr 16	NC_000016.9:g.88727429_88727439del
GRCh37.p13 chr 16	NC_000016.9:g.88727430_88727439del
GRCh37.p13 chr 16	NC_000016.9:g.88727431_88727439del
GRCh37.p13 chr 16	NC_000016.9:g.88727432_88727439del
GRCh37.p13 chr 16	NC_000016.9:g.88727433_88727439del
GRCh37.p13 chr 16	NC_000016.9:g.88727434_88727439del
GRCh37.p13 chr 16	NC_000016.9:g.88727435_88727439del
GRCh37.p13 chr 16	NC_000016.9:g.88727436_88727439del
GRCh37.p13 chr 16	NC_000016.9:g.88727437_88727439del
GRCh37.p13 chr 16	NC_000016.9:g.88727438_88727439del
GRCh37.p13 chr 16	NC_000016.9:g.88727439del
GRCh37.p13 chr 16	NC_000016.9:g.88727439dup
GRCh37.p13 chr 16	NC_000016.9:g.88727438_88727439dup
GRCh37.p13 chr 16	NC_000016.9:g.88727437_88727439dup
GRCh37.p13 chr 16	NC_000016.9:g.88727436_88727439dup
GRCh37.p13 chr 16	NC_000016.9:g.88727435_88727439dup
GRCh37.p13 chr 16	NC_000016.9:g.88727434_88727439dup
GRCh37.p13 chr 16	NC_000016.9:g.88727433_88727439dup
GRCh37.p13 chr 16	NC_000016.9:g.88727432_88727439dup
GRCh37.p13 chr 16	NC_000016.9:g.88727431_88727439dup
MVD RefSeqGene	NG_052674.1:g.7136_7148del
MVD RefSeqGene	NG_052674.1:g.7137_7148del
MVD RefSeqGene	NG_052674.1:g.7138_7148del
MVD RefSeqGene	NG_052674.1:g.7139_7148del
MVD RefSeqGene	NG_052674.1:g.7140_7148del
MVD RefSeqGene	NG_052674.1:g.7141_7148del
MVD RefSeqGene	NG_052674.1:g.7142_7148del
MVD RefSeqGene	NG_052674.1:g.7143_7148del
MVD RefSeqGene	NG_052674.1:g.7144_7148del
MVD RefSeqGene	NG_052674.1:g.7145_7148del
MVD RefSeqGene	NG_052674.1:g.7146_7148del
MVD RefSeqGene	NG_052674.1:g.7147_7148del
MVD RefSeqGene	NG_052674.1:g.7148del
MVD RefSeqGene	NG_052674.1:g.7148dup
MVD RefSeqGene	NG_052674.1:g.7147_7148dup
MVD RefSeqGene	NG_052674.1:g.7146_7148dup
MVD RefSeqGene	NG_052674.1:g.7145_7148dup
MVD RefSeqGene	NG_052674.1:g.7144_7148dup
MVD RefSeqGene	NG_052674.1:g.7143_7148dup
MVD RefSeqGene	NG_052674.1:g.7142_7148dup
MVD RefSeqGene	NG_052674.1:g.7141_7148dup
MVD RefSeqGene	NG_052674.1:g.7140_7148dup

Gene: MVD, mevalonate diphosphate decarboxylase (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MVD transcript	NM_002461.3:c.70+1993_70+… NM_002461.3:c.70+1993_70+2005del	N/A	Intron Variant
MVD transcript variant X1	XM_011523086.3:c.70+1993_… XM_011523086.3:c.70+1993_70+2005del	N/A	Intron Variant
MVD transcript variant X2	XM_011523087.3:c.7+1694_7… XM_011523087.3:c.7+1694_7+1706del	N/A	Intron Variant
MVD transcript variant X3	XM_011523088.3:c.7+1694_7… XM_011523088.3:c.7+1694_7+1706del	N/A	Intron Variant
MVD transcript variant X4	XM_011523089.3:c.-501-381… XM_011523089.3:c.-501-381_-501-369del	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)₂₆=	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)₈	dup(A)₉
GRCh38.p14 chr 16	NC_000016.10:g.88661006_88661031=	NC_000016.10:g.88661019_88661031del	NC_000016.10:g.88661020_88661031del	NC_000016.10:g.88661021_88661031del	NC_000016.10:g.88661022_88661031del	NC_000016.10:g.88661023_88661031del	NC_000016.10:g.88661024_88661031del	NC_000016.10:g.88661025_88661031del	NC_000016.10:g.88661026_88661031del	NC_000016.10:g.88661027_88661031del	NC_000016.10:g.88661028_88661031del	NC_000016.10:g.88661029_88661031del	NC_000016.10:g.88661030_88661031del	NC_000016.10:g.88661031del	NC_000016.10:g.88661031dup	NC_000016.10:g.88661030_88661031dup	NC_000016.10:g.88661029_88661031dup	NC_000016.10:g.88661028_88661031dup	NC_000016.10:g.88661027_88661031dup	NC_000016.10:g.88661026_88661031dup	NC_000016.10:g.88661025_88661031dup	NC_000016.10:g.88661024_88661031dup	NC_000016.10:g.88661023_88661031dup
GRCh37.p13 chr 16	NC_000016.9:g.88727414_88727439=	NC_000016.9:g.88727427_88727439del	NC_000016.9:g.88727428_88727439del	NC_000016.9:g.88727429_88727439del	NC_000016.9:g.88727430_88727439del	NC_000016.9:g.88727431_88727439del	NC_000016.9:g.88727432_88727439del	NC_000016.9:g.88727433_88727439del	NC_000016.9:g.88727434_88727439del	NC_000016.9:g.88727435_88727439del	NC_000016.9:g.88727436_88727439del	NC_000016.9:g.88727437_88727439del	NC_000016.9:g.88727438_88727439del	NC_000016.9:g.88727439del	NC_000016.9:g.88727439dup	NC_000016.9:g.88727438_88727439dup	NC_000016.9:g.88727437_88727439dup	NC_000016.9:g.88727436_88727439dup	NC_000016.9:g.88727435_88727439dup	NC_000016.9:g.88727434_88727439dup	NC_000016.9:g.88727433_88727439dup	NC_000016.9:g.88727432_88727439dup	NC_000016.9:g.88727431_88727439dup
MVD RefSeqGene	NG_052674.1:g.7123_7148=	NG_052674.1:g.7136_7148del	NG_052674.1:g.7137_7148del	NG_052674.1:g.7138_7148del	NG_052674.1:g.7139_7148del	NG_052674.1:g.7140_7148del	NG_052674.1:g.7141_7148del	NG_052674.1:g.7142_7148del	NG_052674.1:g.7143_7148del	NG_052674.1:g.7144_7148del	NG_052674.1:g.7145_7148del	NG_052674.1:g.7146_7148del	NG_052674.1:g.7147_7148del	NG_052674.1:g.7148del	NG_052674.1:g.7148dup	NG_052674.1:g.7147_7148dup	NG_052674.1:g.7146_7148dup	NG_052674.1:g.7145_7148dup	NG_052674.1:g.7144_7148dup	NG_052674.1:g.7143_7148dup	NG_052674.1:g.7142_7148dup	NG_052674.1:g.7141_7148dup	NG_052674.1:g.7140_7148dup
MVD transcript	NM_002461.1:c.70+2005=	NM_002461.1:c.70+1993_70+2005del	NM_002461.1:c.70+1994_70+2005del	NM_002461.1:c.70+1995_70+2005del	NM_002461.1:c.70+1996_70+2005del	NM_002461.1:c.70+1997_70+2005del	NM_002461.1:c.70+1998_70+2005del	NM_002461.1:c.70+1999_70+2005del	NM_002461.1:c.70+2000_70+2005del	NM_002461.1:c.70+2001_70+2005del	NM_002461.1:c.70+2002_70+2005del	NM_002461.1:c.70+2003_70+2005del	NM_002461.1:c.70+2004_70+2005del	NM_002461.1:c.70+2005del	NM_002461.1:c.70+2005dup	NM_002461.1:c.70+2004_70+2005dup	NM_002461.1:c.70+2003_70+2005dup	NM_002461.1:c.70+2002_70+2005dup	NM_002461.1:c.70+2001_70+2005dup	NM_002461.1:c.70+2000_70+2005dup	NM_002461.1:c.70+1999_70+2005dup	NM_002461.1:c.70+1998_70+2005dup	NM_002461.1:c.70+1997_70+2005dup
MVD transcript	NM_002461.3:c.70+2005=	NM_002461.3:c.70+1993_70+2005del	NM_002461.3:c.70+1994_70+2005del	NM_002461.3:c.70+1995_70+2005del	NM_002461.3:c.70+1996_70+2005del	NM_002461.3:c.70+1997_70+2005del	NM_002461.3:c.70+1998_70+2005del	NM_002461.3:c.70+1999_70+2005del	NM_002461.3:c.70+2000_70+2005del	NM_002461.3:c.70+2001_70+2005del	NM_002461.3:c.70+2002_70+2005del	NM_002461.3:c.70+2003_70+2005del	NM_002461.3:c.70+2004_70+2005del	NM_002461.3:c.70+2005del	NM_002461.3:c.70+2005dup	NM_002461.3:c.70+2004_70+2005dup	NM_002461.3:c.70+2003_70+2005dup	NM_002461.3:c.70+2002_70+2005dup	NM_002461.3:c.70+2001_70+2005dup	NM_002461.3:c.70+2000_70+2005dup	NM_002461.3:c.70+1999_70+2005dup	NM_002461.3:c.70+1998_70+2005dup	NM_002461.3:c.70+1997_70+2005dup
MVD transcript variant X1	XM_005256312.1:c.7+1706=	XM_005256312.1:c.7+1694_7+1706del	XM_005256312.1:c.7+1695_7+1706del	XM_005256312.1:c.7+1696_7+1706del	XM_005256312.1:c.7+1697_7+1706del	XM_005256312.1:c.7+1698_7+1706del	XM_005256312.1:c.7+1699_7+1706del	XM_005256312.1:c.7+1700_7+1706del	XM_005256312.1:c.7+1701_7+1706del	XM_005256312.1:c.7+1702_7+1706del	XM_005256312.1:c.7+1703_7+1706del	XM_005256312.1:c.7+1704_7+1706del	XM_005256312.1:c.7+1705_7+1706del	XM_005256312.1:c.7+1706del	XM_005256312.1:c.7+1706dup	XM_005256312.1:c.7+1705_7+1706dup	XM_005256312.1:c.7+1704_7+1706dup	XM_005256312.1:c.7+1703_7+1706dup	XM_005256312.1:c.7+1702_7+1706dup	XM_005256312.1:c.7+1701_7+1706dup	XM_005256312.1:c.7+1700_7+1706dup	XM_005256312.1:c.7+1699_7+1706dup	XM_005256312.1:c.7+1698_7+1706dup
MVD transcript variant X1	XM_011523086.3:c.70+2005=	XM_011523086.3:c.70+1993_70+2005del	XM_011523086.3:c.70+1994_70+2005del	XM_011523086.3:c.70+1995_70+2005del	XM_011523086.3:c.70+1996_70+2005del	XM_011523086.3:c.70+1997_70+2005del	XM_011523086.3:c.70+1998_70+2005del	XM_011523086.3:c.70+1999_70+2005del	XM_011523086.3:c.70+2000_70+2005del	XM_011523086.3:c.70+2001_70+2005del	XM_011523086.3:c.70+2002_70+2005del	XM_011523086.3:c.70+2003_70+2005del	XM_011523086.3:c.70+2004_70+2005del	XM_011523086.3:c.70+2005del	XM_011523086.3:c.70+2005dup	XM_011523086.3:c.70+2004_70+2005dup	XM_011523086.3:c.70+2003_70+2005dup	XM_011523086.3:c.70+2002_70+2005dup	XM_011523086.3:c.70+2001_70+2005dup	XM_011523086.3:c.70+2000_70+2005dup	XM_011523086.3:c.70+1999_70+2005dup	XM_011523086.3:c.70+1998_70+2005dup	XM_011523086.3:c.70+1997_70+2005dup
MVD transcript variant X2	XM_011523087.3:c.7+1706=	XM_011523087.3:c.7+1694_7+1706del	XM_011523087.3:c.7+1695_7+1706del	XM_011523087.3:c.7+1696_7+1706del	XM_011523087.3:c.7+1697_7+1706del	XM_011523087.3:c.7+1698_7+1706del	XM_011523087.3:c.7+1699_7+1706del	XM_011523087.3:c.7+1700_7+1706del	XM_011523087.3:c.7+1701_7+1706del	XM_011523087.3:c.7+1702_7+1706del	XM_011523087.3:c.7+1703_7+1706del	XM_011523087.3:c.7+1704_7+1706del	XM_011523087.3:c.7+1705_7+1706del	XM_011523087.3:c.7+1706del	XM_011523087.3:c.7+1706dup	XM_011523087.3:c.7+1705_7+1706dup	XM_011523087.3:c.7+1704_7+1706dup	XM_011523087.3:c.7+1703_7+1706dup	XM_011523087.3:c.7+1702_7+1706dup	XM_011523087.3:c.7+1701_7+1706dup	XM_011523087.3:c.7+1700_7+1706dup	XM_011523087.3:c.7+1699_7+1706dup	XM_011523087.3:c.7+1698_7+1706dup
MVD transcript variant X3	XM_011523088.3:c.7+1706=	XM_011523088.3:c.7+1694_7+1706del	XM_011523088.3:c.7+1695_7+1706del	XM_011523088.3:c.7+1696_7+1706del	XM_011523088.3:c.7+1697_7+1706del	XM_011523088.3:c.7+1698_7+1706del	XM_011523088.3:c.7+1699_7+1706del	XM_011523088.3:c.7+1700_7+1706del	XM_011523088.3:c.7+1701_7+1706del	XM_011523088.3:c.7+1702_7+1706del	XM_011523088.3:c.7+1703_7+1706del	XM_011523088.3:c.7+1704_7+1706del	XM_011523088.3:c.7+1705_7+1706del	XM_011523088.3:c.7+1706del	XM_011523088.3:c.7+1706dup	XM_011523088.3:c.7+1705_7+1706dup	XM_011523088.3:c.7+1704_7+1706dup	XM_011523088.3:c.7+1703_7+1706dup	XM_011523088.3:c.7+1702_7+1706dup	XM_011523088.3:c.7+1701_7+1706dup	XM_011523088.3:c.7+1700_7+1706dup	XM_011523088.3:c.7+1699_7+1706dup	XM_011523088.3:c.7+1698_7+1706dup
MVD transcript variant X4	XM_011523089.3:c.-501-369=	XM_011523089.3:c.-501-381_-501-369del	XM_011523089.3:c.-501-380_-501-369del	XM_011523089.3:c.-501-379_-501-369del	XM_011523089.3:c.-501-378_-501-369del	XM_011523089.3:c.-501-377_-501-369del	XM_011523089.3:c.-501-376_-501-369del	XM_011523089.3:c.-501-375_-501-369del	XM_011523089.3:c.-501-374_-501-369del	XM_011523089.3:c.-501-373_-501-369del	XM_011523089.3:c.-501-372_-501-369del	XM_011523089.3:c.-501-371_-501-369del	XM_011523089.3:c.-501-370_-501-369del	XM_011523089.3:c.-501-369del	XM_011523089.3:c.-501-369dup	XM_011523089.3:c.-501-370_-501-369dup	XM_011523089.3:c.-501-371_-501-369dup	XM_011523089.3:c.-501-372_-501-369dup	XM_011523089.3:c.-501-373_-501-369dup	XM_011523089.3:c.-501-374_-501-369dup	XM_011523089.3:c.-501-375_-501-369dup	XM_011523089.3:c.-501-376_-501-369dup	XM_011523089.3:c.-501-377_-501-369dup

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#.

58 SubSNP, 34 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80358121	Dec 15, 2007 (129)
2	HGSV	ss83607820	Dec 15, 2007 (129)
3	HUMANGENOME_JCVI	ss95685053	Oct 12, 2018 (152)
4	GMI	ss289309900	May 04, 2012 (137)
5	PJP	ss294900312	Oct 12, 2018 (152)
6	PJP	ss294900313	Jan 10, 2018 (151)
7	1000GENOMES	ss1376231307	Aug 21, 2014 (142)
8	SWEGEN	ss3015019152	Nov 08, 2017 (151)
9	EVA_DECODE	ss3699877670	Jul 13, 2019 (153)
10	EVA_DECODE	ss3699877671	Jul 13, 2019 (153)
11	EVA_DECODE	ss3699877672	Jul 13, 2019 (153)
12	EVA_DECODE	ss3699877673	Jul 13, 2019 (153)
13	KHV_HUMAN_GENOMES	ss3819597366	Jul 13, 2019 (153)
14	EVA	ss3834725995	Apr 27, 2020 (154)
15	GNOMAD	ss4306273704	Apr 26, 2021 (155)
16	GNOMAD	ss4306273705	Apr 26, 2021 (155)
17	GNOMAD	ss4306273706	Apr 26, 2021 (155)
18	GNOMAD	ss4306273707	Apr 26, 2021 (155)
19	GNOMAD	ss4306273708	Apr 26, 2021 (155)
20	GNOMAD	ss4306273709	Apr 26, 2021 (155)
21	GNOMAD	ss4306273710	Apr 26, 2021 (155)
22	GNOMAD	ss4306273711	Apr 26, 2021 (155)
23	GNOMAD	ss4306273712	Apr 26, 2021 (155)
24	GNOMAD	ss4306273713	Apr 26, 2021 (155)
25	GNOMAD	ss4306273714	Apr 26, 2021 (155)
26	GNOMAD	ss4306273715	Apr 26, 2021 (155)
27	GNOMAD	ss4306273716	Apr 26, 2021 (155)
28	GNOMAD	ss4306273717	Apr 26, 2021 (155)
29	GNOMAD	ss4306273718	Apr 26, 2021 (155)
30	GNOMAD	ss4306273719	Apr 26, 2021 (155)
31	GNOMAD	ss4306273720	Apr 26, 2021 (155)
32	GNOMAD	ss4306273721	Apr 26, 2021 (155)
33	GNOMAD	ss4306273722	Apr 26, 2021 (155)
34	GNOMAD	ss4306273723	Apr 26, 2021 (155)
35	GNOMAD	ss4306273724	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5220997584	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5220997585	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5220997586	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5220997587	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5220997588	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5220997589	Apr 26, 2021 (155)
42	1000G_HIGH_COVERAGE	ss5302056790	Oct 16, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5302056791	Oct 16, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5302056792	Oct 16, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5302056793	Oct 16, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5302056794	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5495286076	Oct 16, 2022 (156)
48	HUGCELL_USP	ss5495286077	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5495286078	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5495286079	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5495286080	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5776424210	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5776424211	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5776424212	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5776424214	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5776424215	Oct 16, 2022 (156)
57	EVA	ss5846840095	Oct 16, 2022 (156)
58	EVA	ss5846840096	Oct 16, 2022 (156)
59	1000Genomes	NC_000016.9 - 88727414	Oct 12, 2018 (152)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498601580 (NC_000016.10:88661005::A 30570/47002) Row 498601581 (NC_000016.10:88661005::AA 735/47096) Row 498601582 (NC_000016.10:88661005::AAA 29/47162)...	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 78966891 (NC_000016.9:88727413:AAAAAAAAAAA: 650/15106) Row 78966892 (NC_000016.9:88727413:AAAAAAAAA: 65/15106) Row 78966893 (NC_000016.9:88727413::A 4647/15106)...	-	Apr 26, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 78966891 (NC_000016.9:88727413:AAAAAAAAAAA: 650/15106) Row 78966892 (NC_000016.9:88727413:AAAAAAAAA: 65/15106) Row 78966893 (NC_000016.9:88727413::A 4647/15106)...	-	Apr 26, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 78966891 (NC_000016.9:88727413:AAAAAAAAAAA: 650/15106) Row 78966892 (NC_000016.9:88727413:AAAAAAAAA: 65/15106) Row 78966893 (NC_000016.9:88727413::A 4647/15106)...	-	Apr 26, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 78966891 (NC_000016.9:88727413:AAAAAAAAAAA: 650/15106) Row 78966892 (NC_000016.9:88727413:AAAAAAAAA: 65/15106) Row 78966893 (NC_000016.9:88727413::A 4647/15106)...	-	Apr 26, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 78966891 (NC_000016.9:88727413:AAAAAAAAAAA: 650/15106) Row 78966892 (NC_000016.9:88727413:AAAAAAAAA: 65/15106) Row 78966893 (NC_000016.9:88727413::A 4647/15106)...	-	Apr 26, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 78966891 (NC_000016.9:88727413:AAAAAAAAAAA: 650/15106) Row 78966892 (NC_000016.9:88727413:AAAAAAAAA: 65/15106) Row 78966893 (NC_000016.9:88727413::A 4647/15106)...	-	Apr 26, 2021 (155)
87	14KJPN Submission ignored due to conflicting rows: Row 110261314 (NC_000016.10:88661005:AAAAAAAAAAA: 1178/26642) Row 110261315 (NC_000016.10:88661005:AAAAAAAAA: 154/26642) Row 110261316 (NC_000016.10:88661005::A 9704/26642)...	-	Oct 16, 2022 (156)
88	14KJPN Submission ignored due to conflicting rows: Row 110261314 (NC_000016.10:88661005:AAAAAAAAAAA: 1178/26642) Row 110261315 (NC_000016.10:88661005:AAAAAAAAA: 154/26642) Row 110261316 (NC_000016.10:88661005::A 9704/26642)...	-	Oct 16, 2022 (156)
89	14KJPN Submission ignored due to conflicting rows: Row 110261314 (NC_000016.10:88661005:AAAAAAAAAAA: 1178/26642) Row 110261315 (NC_000016.10:88661005:AAAAAAAAA: 154/26642) Row 110261316 (NC_000016.10:88661005::A 9704/26642)...	-	Oct 16, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 110261314 (NC_000016.10:88661005:AAAAAAAAAAA: 1178/26642) Row 110261315 (NC_000016.10:88661005:AAAAAAAAA: 154/26642) Row 110261316 (NC_000016.10:88661005::A 9704/26642)...	-	Oct 16, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 110261314 (NC_000016.10:88661005:AAAAAAAAAAA: 1178/26642) Row 110261315 (NC_000016.10:88661005:AAAAAAAAA: 154/26642) Row 110261316 (NC_000016.10:88661005::A 9704/26642)...	-	Oct 16, 2022 (156)
92	ALFA	NC_000016.10 - 88661006	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
ss5846840096	NC_000016.9:88727413:AAAAAAAAAAAAA:	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA
ss4306273724	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAA:	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
13181468367	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4306273723	NC_000016.10:88661005:AAAAAAAAAAAA:	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
13181468367	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss289309900	NC_000016.8:87254914:AAAAAAAAAAA:	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
70705607, ss1376231307, ss3015019152, ss5220997584	NC_000016.9:88727413:AAAAAAAAAAA:	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3819597366, ss4306273722, ss5302056793, ss5495286080, ss5776424210	NC_000016.10:88661005:AAAAAAAAAAA:	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
13181468367	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4306273721	NC_000016.10:88661005:AAAAAAAAAA:	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
13181468367	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5220997585	NC_000016.9:88727413:AAAAAAAAA:	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4306273720, ss5302056792, ss5495286079, ss5776424211	NC_000016.10:88661005:AAAAAAAAA:	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
13181468367	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4306273719	NC_000016.10:88661005:AAAAAAAA:	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
13181468367	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4306273718	NC_000016.10:88661005:AAAAAAA:	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
13181468367	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5220997589	NC_000016.9:88727413:AAAAAA:	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4306273717, ss5776424215	NC_000016.10:88661005:AAAAAA:	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
13181468367	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4306273716	NC_000016.10:88661005:AAAAA:	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
13181468367	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4306273715	NC_000016.10:88661005:AAAA:	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
13181468367	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
13181468367	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4306273714	NC_000016.10:88661005:AA:	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
13181468367	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss80358121, ss83607820	NC_000016.8:87254939:A:	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5220997588	NC_000016.9:88727413:A:	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3699877673, ss4306273713, ss5302056790, ss5495286077	NC_000016.10:88661005:A:	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13181468367	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss294900312	NC_000016.8:87254915::A	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss294900313	NC_000016.8:87254940::A	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5220997586	NC_000016.9:88727413::A	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4306273704, ss5495286076, ss5776424212	NC_000016.10:88661005::A	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13181468367	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3699877672	NC_000016.10:88661006::A	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss95685053	NT_010542.15:288056::A	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5220997587, ss5846840095	NC_000016.9:88727413::AA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4306273705, ss5302056791, ss5495286078, ss5776424214	NC_000016.10:88661005::AA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13181468367	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3699877671	NC_000016.10:88661006::AA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4306273706	NC_000016.10:88661005::AAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13181468367	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3834725995	NC_000016.9:88727413::AAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4306273707	NC_000016.10:88661005::AAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13181468367	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4306273708, ss5302056794	NC_000016.10:88661005::AAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13181468367	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3699877670	NC_000016.10:88661006::AAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4306273709	NC_000016.10:88661005::AAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13181468367	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4306273710	NC_000016.10:88661005::AAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13181468367	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4306273711	NC_000016.10:88661005::AAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4306273712	NC_000016.10:88661005::AAAAAAAAA	NC_000016.10:88661005:AAAAAAAAAAAA… NC_000016.10:88661005:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs60124992

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

rs60124992