Name: rs59878175
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.

rs59878175

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:31125730-31125756 (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)₁₆ / del(A)₁₅ / del(A)₁₃ / d…
del(A)₁₆ / del(A)₁₅ / 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)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₆=0.0000 (0/3878, ALFA)
del(A)₁₅=0.0000 (0/3878, ALFA)
del(A)₁₃=0.0000 (0/3878, ALFA) (+ 17 more)
del(A)₁₂=0.0000 (0/3878, ALFA)
del(A)₁₁=0.0000 (0/3878, ALFA)
del(A)₁₀=0.0000 (0/3878, ALFA)
del(A)₉=0.0000 (0/3878, ALFA)
del(A)₈=0.0000 (0/3878, ALFA)
del(A)₇=0.0000 (0/3878, ALFA)
del(A)₆=0.0000 (0/3878, ALFA)
del(A)₅=0.0000 (0/3878, ALFA)
del(A)₄=0.0000 (0/3878, ALFA)
delAAA=0.0000 (0/3878, ALFA)
delAA=0.0000 (0/3878, ALFA)
delA=0.0000 (0/3878, ALFA)
dupA=0.0000 (0/3878, ALFA)
dupAA=0.0000 (0/3878, ALFA)
dupAAA=0.0000 (0/3878, ALFA)
dup(A)₄=0.0000 (0/3878, ALFA)
del(A)₅=0.17 (7/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TRPM1 : 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	3878	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	2658	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	764	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	34	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	730	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	6	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
East Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Other Asian	Sub	2	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	56	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	206	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	36	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	152	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	3878	(A)₂₇=1.0000	del(A)₁₆=0.0000, del(A)₁₅=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)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
Allele Frequency Aggregator	European	Sub	2658	(A)₂₇=1.0000	del(A)₁₆=0.0000, del(A)₁₅=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)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
Allele Frequency Aggregator	African	Sub	764	(A)₂₇=1.000	del(A)₁₆=0.000, del(A)₁₅=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)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
Allele Frequency Aggregator	Latin American 2	Sub	206	(A)₂₇=1.000	del(A)₁₆=0.000, del(A)₁₅=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)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
Allele Frequency Aggregator	Other	Sub	152	(A)₂₇=1.000	del(A)₁₆=0.000, del(A)₁₅=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)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
Allele Frequency Aggregator	Latin American 1	Sub	56	(A)₂₇=1.00	del(A)₁₆=0.00, del(A)₁₅=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)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
Allele Frequency Aggregator	South Asian	Sub	36	(A)₂₇=1.00	del(A)₁₆=0.00, del(A)₁₅=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)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
Allele Frequency Aggregator	Asian	Sub	6	(A)₂₇=1.0	del(A)₁₆=0.0, del(A)₁₅=0.0, del(A)₁₃=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0
The Danish reference pan genome	Danish	Study-wide	40	(A)₂₇=0.82	del(A)₅=0.17

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 15	NC_000015.10:g.31125741_31125756del
GRCh38.p14 chr 15	NC_000015.10:g.31125742_31125756del
GRCh38.p14 chr 15	NC_000015.10:g.31125744_31125756del
GRCh38.p14 chr 15	NC_000015.10:g.31125745_31125756del
GRCh38.p14 chr 15	NC_000015.10:g.31125746_31125756del
GRCh38.p14 chr 15	NC_000015.10:g.31125747_31125756del
GRCh38.p14 chr 15	NC_000015.10:g.31125748_31125756del
GRCh38.p14 chr 15	NC_000015.10:g.31125749_31125756del
GRCh38.p14 chr 15	NC_000015.10:g.31125750_31125756del
GRCh38.p14 chr 15	NC_000015.10:g.31125751_31125756del
GRCh38.p14 chr 15	NC_000015.10:g.31125752_31125756del
GRCh38.p14 chr 15	NC_000015.10:g.31125753_31125756del
GRCh38.p14 chr 15	NC_000015.10:g.31125754_31125756del
GRCh38.p14 chr 15	NC_000015.10:g.31125755_31125756del
GRCh38.p14 chr 15	NC_000015.10:g.31125756del
GRCh38.p14 chr 15	NC_000015.10:g.31125756dup
GRCh38.p14 chr 15	NC_000015.10:g.31125755_31125756dup
GRCh38.p14 chr 15	NC_000015.10:g.31125754_31125756dup
GRCh38.p14 chr 15	NC_000015.10:g.31125753_31125756dup
GRCh38.p14 chr 15	NC_000015.10:g.31125752_31125756dup
GRCh38.p14 chr 15	NC_000015.10:g.31125751_31125756dup
GRCh38.p14 chr 15	NC_000015.10:g.31125747_31125756dup
GRCh37.p13 chr 15	NC_000015.9:g.31417944_31417959del
GRCh37.p13 chr 15	NC_000015.9:g.31417945_31417959del
GRCh37.p13 chr 15	NC_000015.9:g.31417947_31417959del
GRCh37.p13 chr 15	NC_000015.9:g.31417948_31417959del
GRCh37.p13 chr 15	NC_000015.9:g.31417949_31417959del
GRCh37.p13 chr 15	NC_000015.9:g.31417950_31417959del
GRCh37.p13 chr 15	NC_000015.9:g.31417951_31417959del
GRCh37.p13 chr 15	NC_000015.9:g.31417952_31417959del
GRCh37.p13 chr 15	NC_000015.9:g.31417953_31417959del
GRCh37.p13 chr 15	NC_000015.9:g.31417954_31417959del
GRCh37.p13 chr 15	NC_000015.9:g.31417955_31417959del
GRCh37.p13 chr 15	NC_000015.9:g.31417956_31417959del
GRCh37.p13 chr 15	NC_000015.9:g.31417957_31417959del
GRCh37.p13 chr 15	NC_000015.9:g.31417958_31417959del
GRCh37.p13 chr 15	NC_000015.9:g.31417959del
GRCh37.p13 chr 15	NC_000015.9:g.31417959dup
GRCh37.p13 chr 15	NC_000015.9:g.31417958_31417959dup
GRCh37.p13 chr 15	NC_000015.9:g.31417957_31417959dup
GRCh37.p13 chr 15	NC_000015.9:g.31417956_31417959dup
GRCh37.p13 chr 15	NC_000015.9:g.31417955_31417959dup
GRCh37.p13 chr 15	NC_000015.9:g.31417954_31417959dup
GRCh37.p13 chr 15	NC_000015.9:g.31417950_31417959dup
TRPM1 RefSeqGene	NG_016453.2:g.40529_40544del
TRPM1 RefSeqGene	NG_016453.2:g.40530_40544del
TRPM1 RefSeqGene	NG_016453.2:g.40532_40544del
TRPM1 RefSeqGene	NG_016453.2:g.40533_40544del
TRPM1 RefSeqGene	NG_016453.2:g.40534_40544del
TRPM1 RefSeqGene	NG_016453.2:g.40535_40544del
TRPM1 RefSeqGene	NG_016453.2:g.40536_40544del
TRPM1 RefSeqGene	NG_016453.2:g.40537_40544del
TRPM1 RefSeqGene	NG_016453.2:g.40538_40544del
TRPM1 RefSeqGene	NG_016453.2:g.40539_40544del
TRPM1 RefSeqGene	NG_016453.2:g.40540_40544del
TRPM1 RefSeqGene	NG_016453.2:g.40541_40544del
TRPM1 RefSeqGene	NG_016453.2:g.40542_40544del
TRPM1 RefSeqGene	NG_016453.2:g.40543_40544del
TRPM1 RefSeqGene	NG_016453.2:g.40544del
TRPM1 RefSeqGene	NG_016453.2:g.40544dup
TRPM1 RefSeqGene	NG_016453.2:g.40543_40544dup
TRPM1 RefSeqGene	NG_016453.2:g.40542_40544dup
TRPM1 RefSeqGene	NG_016453.2:g.40541_40544dup
TRPM1 RefSeqGene	NG_016453.2:g.40540_40544dup
TRPM1 RefSeqGene	NG_016453.2:g.40539_40544dup
TRPM1 RefSeqGene	NG_016453.2:g.40535_40544dup
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299032_3299047del
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299033_3299047del
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299035_3299047del
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299036_3299047del
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299037_3299047del
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299038_3299047del
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299039_3299047del
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299040_3299047del
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299041_3299047del
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299042_3299047del
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299043_3299047del
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299044_3299047del
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299045_3299047del
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299046_3299047del
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299047del
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299047dup
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299046_3299047dup
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299045_3299047dup
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299044_3299047dup
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299043_3299047dup
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299042_3299047dup
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299038_3299047dup
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411484_3411499del
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411485_3411499del
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411487_3411499del
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411488_3411499del
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411489_3411499del
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411490_3411499del
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411491_3411499del
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411492_3411499del
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411493_3411499del
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411494_3411499del
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411495_3411499del
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411496_3411499del
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411497_3411499del
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411498_3411499del
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411499del
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411499dup
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411498_3411499dup
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411497_3411499dup
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411496_3411499dup
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411495_3411499dup
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411494_3411499dup
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411490_3411499dup

Gene: TRPM1, transient receptor potential cation channel subfamily M member 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TRPM1 transcript variant 1	NM_001252020.2:c.54+35161… NM_001252020.2:c.54+35161_54+35176del	N/A	Intron Variant
TRPM1 transcript variant 3	NM_001252024.2:c.	N/A	Genic Upstream Transcript Variant
TRPM1 transcript variant 4	NM_001252030.2:c.	N/A	Genic Upstream Transcript Variant
TRPM1 transcript variant 2	NM_002420.6:c.	N/A	Genic Upstream Transcript 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)₂₇=	del(A)₁₆	del(A)₁₅	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)₁₀
GRCh38.p14 chr 15	NC_000015.10:g.31125730_31125756=	NC_000015.10:g.31125741_31125756del	NC_000015.10:g.31125742_31125756del	NC_000015.10:g.31125744_31125756del	NC_000015.10:g.31125745_31125756del	NC_000015.10:g.31125746_31125756del	NC_000015.10:g.31125747_31125756del	NC_000015.10:g.31125748_31125756del	NC_000015.10:g.31125749_31125756del	NC_000015.10:g.31125750_31125756del	NC_000015.10:g.31125751_31125756del	NC_000015.10:g.31125752_31125756del	NC_000015.10:g.31125753_31125756del	NC_000015.10:g.31125754_31125756del	NC_000015.10:g.31125755_31125756del	NC_000015.10:g.31125756del	NC_000015.10:g.31125756dup	NC_000015.10:g.31125755_31125756dup	NC_000015.10:g.31125754_31125756dup	NC_000015.10:g.31125753_31125756dup	NC_000015.10:g.31125752_31125756dup	NC_000015.10:g.31125751_31125756dup	NC_000015.10:g.31125747_31125756dup
GRCh37.p13 chr 15	NC_000015.9:g.31417933_31417959=	NC_000015.9:g.31417944_31417959del	NC_000015.9:g.31417945_31417959del	NC_000015.9:g.31417947_31417959del	NC_000015.9:g.31417948_31417959del	NC_000015.9:g.31417949_31417959del	NC_000015.9:g.31417950_31417959del	NC_000015.9:g.31417951_31417959del	NC_000015.9:g.31417952_31417959del	NC_000015.9:g.31417953_31417959del	NC_000015.9:g.31417954_31417959del	NC_000015.9:g.31417955_31417959del	NC_000015.9:g.31417956_31417959del	NC_000015.9:g.31417957_31417959del	NC_000015.9:g.31417958_31417959del	NC_000015.9:g.31417959del	NC_000015.9:g.31417959dup	NC_000015.9:g.31417958_31417959dup	NC_000015.9:g.31417957_31417959dup	NC_000015.9:g.31417956_31417959dup	NC_000015.9:g.31417955_31417959dup	NC_000015.9:g.31417954_31417959dup	NC_000015.9:g.31417950_31417959dup
TRPM1 RefSeqGene	NG_016453.2:g.40518_40544=	NG_016453.2:g.40529_40544del	NG_016453.2:g.40530_40544del	NG_016453.2:g.40532_40544del	NG_016453.2:g.40533_40544del	NG_016453.2:g.40534_40544del	NG_016453.2:g.40535_40544del	NG_016453.2:g.40536_40544del	NG_016453.2:g.40537_40544del	NG_016453.2:g.40538_40544del	NG_016453.2:g.40539_40544del	NG_016453.2:g.40540_40544del	NG_016453.2:g.40541_40544del	NG_016453.2:g.40542_40544del	NG_016453.2:g.40543_40544del	NG_016453.2:g.40544del	NG_016453.2:g.40544dup	NG_016453.2:g.40543_40544dup	NG_016453.2:g.40542_40544dup	NG_016453.2:g.40541_40544dup	NG_016453.2:g.40540_40544dup	NG_016453.2:g.40539_40544dup	NG_016453.2:g.40535_40544dup
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.3299021_3299047=	NW_011332701.1:g.3299032_3299047del	NW_011332701.1:g.3299033_3299047del	NW_011332701.1:g.3299035_3299047del	NW_011332701.1:g.3299036_3299047del	NW_011332701.1:g.3299037_3299047del	NW_011332701.1:g.3299038_3299047del	NW_011332701.1:g.3299039_3299047del	NW_011332701.1:g.3299040_3299047del	NW_011332701.1:g.3299041_3299047del	NW_011332701.1:g.3299042_3299047del	NW_011332701.1:g.3299043_3299047del	NW_011332701.1:g.3299044_3299047del	NW_011332701.1:g.3299045_3299047del	NW_011332701.1:g.3299046_3299047del	NW_011332701.1:g.3299047del	NW_011332701.1:g.3299047dup	NW_011332701.1:g.3299046_3299047dup	NW_011332701.1:g.3299045_3299047dup	NW_011332701.1:g.3299044_3299047dup	NW_011332701.1:g.3299043_3299047dup	NW_011332701.1:g.3299042_3299047dup	NW_011332701.1:g.3299038_3299047dup
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.3411473_3411499=	NT_187660.1:g.3411484_3411499del	NT_187660.1:g.3411485_3411499del	NT_187660.1:g.3411487_3411499del	NT_187660.1:g.3411488_3411499del	NT_187660.1:g.3411489_3411499del	NT_187660.1:g.3411490_3411499del	NT_187660.1:g.3411491_3411499del	NT_187660.1:g.3411492_3411499del	NT_187660.1:g.3411493_3411499del	NT_187660.1:g.3411494_3411499del	NT_187660.1:g.3411495_3411499del	NT_187660.1:g.3411496_3411499del	NT_187660.1:g.3411497_3411499del	NT_187660.1:g.3411498_3411499del	NT_187660.1:g.3411499del	NT_187660.1:g.3411499dup	NT_187660.1:g.3411498_3411499dup	NT_187660.1:g.3411497_3411499dup	NT_187660.1:g.3411496_3411499dup	NT_187660.1:g.3411495_3411499dup	NT_187660.1:g.3411494_3411499dup	NT_187660.1:g.3411490_3411499dup
TRPM1 transcript variant 1	NM_001252020.1:c.54+35176=	NM_001252020.1:c.54+35161_54+35176del	NM_001252020.1:c.54+35162_54+35176del	NM_001252020.1:c.54+35164_54+35176del	NM_001252020.1:c.54+35165_54+35176del	NM_001252020.1:c.54+35166_54+35176del	NM_001252020.1:c.54+35167_54+35176del	NM_001252020.1:c.54+35168_54+35176del	NM_001252020.1:c.54+35169_54+35176del	NM_001252020.1:c.54+35170_54+35176del	NM_001252020.1:c.54+35171_54+35176del	NM_001252020.1:c.54+35172_54+35176del	NM_001252020.1:c.54+35173_54+35176del	NM_001252020.1:c.54+35174_54+35176del	NM_001252020.1:c.54+35175_54+35176del	NM_001252020.1:c.54+35176del	NM_001252020.1:c.54+35176dup	NM_001252020.1:c.54+35175_54+35176dup	NM_001252020.1:c.54+35174_54+35176dup	NM_001252020.1:c.54+35173_54+35176dup	NM_001252020.1:c.54+35172_54+35176dup	NM_001252020.1:c.54+35171_54+35176dup	NM_001252020.1:c.54+35167_54+35176dup
TRPM1 transcript variant 1	NM_001252020.2:c.54+35176=	NM_001252020.2:c.54+35161_54+35176del	NM_001252020.2:c.54+35162_54+35176del	NM_001252020.2:c.54+35164_54+35176del	NM_001252020.2:c.54+35165_54+35176del	NM_001252020.2:c.54+35166_54+35176del	NM_001252020.2:c.54+35167_54+35176del	NM_001252020.2:c.54+35168_54+35176del	NM_001252020.2:c.54+35169_54+35176del	NM_001252020.2:c.54+35170_54+35176del	NM_001252020.2:c.54+35171_54+35176del	NM_001252020.2:c.54+35172_54+35176del	NM_001252020.2:c.54+35173_54+35176del	NM_001252020.2:c.54+35174_54+35176del	NM_001252020.2:c.54+35175_54+35176del	NM_001252020.2:c.54+35176del	NM_001252020.2:c.54+35176dup	NM_001252020.2:c.54+35175_54+35176dup	NM_001252020.2:c.54+35174_54+35176dup	NM_001252020.2:c.54+35173_54+35176dup	NM_001252020.2:c.54+35172_54+35176dup	NM_001252020.2:c.54+35171_54+35176dup	NM_001252020.2:c.54+35167_54+35176dup

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#.

52 SubSNP, 27 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss82514697	Dec 15, 2007 (129)
2	HUMANGENOME_JCVI	ss95654333	Mar 15, 2016 (147)
3	EVA_GENOME_DK	ss1574839246	Apr 01, 2015 (144)
4	SWEGEN	ss3013044314	Nov 08, 2017 (151)
5	URBANLAB	ss3650321952	Oct 12, 2018 (152)
6	EVA_DECODE	ss3697616411	Jul 13, 2019 (153)
7	EVA_DECODE	ss3697616412	Jul 13, 2019 (153)
8	EVA_DECODE	ss3697616413	Jul 13, 2019 (153)
9	EVA_DECODE	ss3697616414	Jul 13, 2019 (153)
10	EVA_DECODE	ss3697616415	Jul 13, 2019 (153)
11	EVA_DECODE	ss3697616416	Jul 13, 2019 (153)
12	PACBIO	ss3787805377	Jul 13, 2019 (153)
13	PACBIO	ss3792823856	Jul 13, 2019 (153)
14	PACBIO	ss3792823857	Jul 13, 2019 (153)
15	PACBIO	ss3797708310	Jul 13, 2019 (153)
16	PACBIO	ss3797708311	Jul 13, 2019 (153)
17	EVA	ss3834163946	Apr 27, 2020 (154)
18	GNOMAD	ss4286255787	Apr 26, 2021 (155)
19	GNOMAD	ss4286255788	Apr 26, 2021 (155)
20	GNOMAD	ss4286255789	Apr 26, 2021 (155)
21	GNOMAD	ss4286255790	Apr 26, 2021 (155)
22	GNOMAD	ss4286255791	Apr 26, 2021 (155)
23	GNOMAD	ss4286255792	Apr 26, 2021 (155)
24	GNOMAD	ss4286255793	Apr 26, 2021 (155)
25	GNOMAD	ss4286255794	Apr 26, 2021 (155)
26	GNOMAD	ss4286255795	Apr 26, 2021 (155)
27	GNOMAD	ss4286255796	Apr 26, 2021 (155)
28	GNOMAD	ss4286255797	Apr 26, 2021 (155)
29	GNOMAD	ss4286255798	Apr 26, 2021 (155)
30	GNOMAD	ss4286255799	Apr 26, 2021 (155)
31	GNOMAD	ss4286255800	Apr 26, 2021 (155)
32	GNOMAD	ss4286255801	Apr 26, 2021 (155)
33	GNOMAD	ss4286255802	Apr 26, 2021 (155)
34	GNOMAD	ss4286255803	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5215516728	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5215516729	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5215516730	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5215516731	Apr 26, 2021 (155)
39	1000G_HIGH_COVERAGE	ss5297935096	Oct 16, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5297935097	Oct 16, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5297935098	Oct 16, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5297935099	Oct 16, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5297935100	Oct 16, 2022 (156)
44	HUGCELL_USP	ss5491725824	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5491725825	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5491725826	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5491725827	Oct 16, 2022 (156)
48	HUGCELL_USP	ss5491725828	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5769122616	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5769122617	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5769122618	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5769122619	Oct 16, 2022 (156)
53	The Danish reference pan genome	NC_000015.9 - 31417933	Apr 27, 2020 (154)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464843140 (NC_000015.10:31125729::A 5665/49450) Row 464843141 (NC_000015.10:31125729::AA 806/49504) Row 464843142 (NC_000015.10:31125729::AAA 25/49532)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464843140 (NC_000015.10:31125729::A 5665/49450) Row 464843141 (NC_000015.10:31125729::AA 806/49504) Row 464843142 (NC_000015.10:31125729::AAA 25/49532)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464843140 (NC_000015.10:31125729::A 5665/49450) Row 464843141 (NC_000015.10:31125729::AA 806/49504) Row 464843142 (NC_000015.10:31125729::AAA 25/49532)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464843140 (NC_000015.10:31125729::A 5665/49450) Row 464843141 (NC_000015.10:31125729::AA 806/49504) Row 464843142 (NC_000015.10:31125729::AAA 25/49532)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464843140 (NC_000015.10:31125729::A 5665/49450) Row 464843141 (NC_000015.10:31125729::AA 806/49504) Row 464843142 (NC_000015.10:31125729::AAA 25/49532)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464843140 (NC_000015.10:31125729::A 5665/49450) Row 464843141 (NC_000015.10:31125729::AA 806/49504) Row 464843142 (NC_000015.10:31125729::AAA 25/49532)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464843140 (NC_000015.10:31125729::A 5665/49450) Row 464843141 (NC_000015.10:31125729::AA 806/49504) Row 464843142 (NC_000015.10:31125729::AAA 25/49532)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464843140 (NC_000015.10:31125729::A 5665/49450) Row 464843141 (NC_000015.10:31125729::AA 806/49504) Row 464843142 (NC_000015.10:31125729::AAA 25/49532)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464843140 (NC_000015.10:31125729::A 5665/49450) Row 464843141 (NC_000015.10:31125729::AA 806/49504) Row 464843142 (NC_000015.10:31125729::AAA 25/49532)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464843140 (NC_000015.10:31125729::A 5665/49450) Row 464843141 (NC_000015.10:31125729::AA 806/49504) Row 464843142 (NC_000015.10:31125729::AAA 25/49532)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464843140 (NC_000015.10:31125729::A 5665/49450) Row 464843141 (NC_000015.10:31125729::AA 806/49504) Row 464843142 (NC_000015.10:31125729::AAA 25/49532)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464843140 (NC_000015.10:31125729::A 5665/49450) Row 464843141 (NC_000015.10:31125729::AA 806/49504) Row 464843142 (NC_000015.10:31125729::AAA 25/49532)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464843140 (NC_000015.10:31125729::A 5665/49450) Row 464843141 (NC_000015.10:31125729::AA 806/49504) Row 464843142 (NC_000015.10:31125729::AAA 25/49532)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464843140 (NC_000015.10:31125729::A 5665/49450) Row 464843141 (NC_000015.10:31125729::AA 806/49504) Row 464843142 (NC_000015.10:31125729::AAA 25/49532)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464843140 (NC_000015.10:31125729::A 5665/49450) Row 464843141 (NC_000015.10:31125729::AA 806/49504) Row 464843142 (NC_000015.10:31125729::AAA 25/49532)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464843140 (NC_000015.10:31125729::A 5665/49450) Row 464843141 (NC_000015.10:31125729::AA 806/49504) Row 464843142 (NC_000015.10:31125729::AAA 25/49532)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464843140 (NC_000015.10:31125729::A 5665/49450) Row 464843141 (NC_000015.10:31125729::AA 806/49504) Row 464843142 (NC_000015.10:31125729::AAA 25/49532)...	-	Apr 26, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 73486035 (NC_000015.9:31417932::A 5609/12000) Row 73486036 (NC_000015.9:31417932:AAAAA: 896/12000) Row 73486037 (NC_000015.9:31417932::AA 549/12000)...	-	Apr 26, 2021 (155)
72	8.3KJPN Submission ignored due to conflicting rows: Row 73486035 (NC_000015.9:31417932::A 5609/12000) Row 73486036 (NC_000015.9:31417932:AAAAA: 896/12000) Row 73486037 (NC_000015.9:31417932::AA 549/12000)...	-	Apr 26, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 73486035 (NC_000015.9:31417932::A 5609/12000) Row 73486036 (NC_000015.9:31417932:AAAAA: 896/12000) Row 73486037 (NC_000015.9:31417932::AA 549/12000)...	-	Apr 26, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 73486035 (NC_000015.9:31417932::A 5609/12000) Row 73486036 (NC_000015.9:31417932:AAAAA: 896/12000) Row 73486037 (NC_000015.9:31417932::AA 549/12000)...	-	Apr 26, 2021 (155)
75	14KJPN Submission ignored due to conflicting rows: Row 102959720 (NC_000015.10:31125729:AAAAA: 1478/18894) Row 102959721 (NC_000015.10:31125729::A 8582/18894) Row 102959722 (NC_000015.10:31125729::AA 749/18894)...	-	Oct 16, 2022 (156)
76	14KJPN Submission ignored due to conflicting rows: Row 102959720 (NC_000015.10:31125729:AAAAA: 1478/18894) Row 102959721 (NC_000015.10:31125729::A 8582/18894) Row 102959722 (NC_000015.10:31125729::AA 749/18894)...	-	Oct 16, 2022 (156)
77	14KJPN Submission ignored due to conflicting rows: Row 102959720 (NC_000015.10:31125729:AAAAA: 1478/18894) Row 102959721 (NC_000015.10:31125729::A 8582/18894) Row 102959722 (NC_000015.10:31125729::AA 749/18894)...	-	Oct 16, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 102959720 (NC_000015.10:31125729:AAAAA: 1478/18894) Row 102959721 (NC_000015.10:31125729::A 8582/18894) Row 102959722 (NC_000015.10:31125729::AA 749/18894)...	-	Oct 16, 2022 (156)
79	ALFA	NC_000015.10 - 31125730	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
ss4286255803	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
8317486507	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss5215516731	NC_000015.9:31417932:AAAAAAAAAAAAA… NC_000015.9:31417932:AAAAAAAAAAAAAAA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss5769122619	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
8317486507	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4286255802	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
8317486507	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3013044314	NC_000015.9:31417932:AAAAAAAAAAAA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4286255801	NC_000015.10:31125729:AAAAAAAAAAAA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
8317486507	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4286255800	NC_000015.10:31125729:AAAAAAAAAAA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
8317486507	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4286255799	NC_000015.10:31125729:AAAAAAAAAA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
8317486507	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4286255798	NC_000015.10:31125729:AAAAAAAAA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
8317486507	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4286255797	NC_000015.10:31125729:AAAAAAAA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
8317486507	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4286255796, ss5297935099	NC_000015.10:31125729:AAAAAAA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
8317486507	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3697616416	NC_000015.10:31125729:AAAAAA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
8317486507	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
479985, ss1574839246, ss3792823856, ss3797708310, ss3834163946, ss5215516729	NC_000015.9:31417932:AAAAA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3650321952, ss5297935097, ss5491725824, ss5769122616	NC_000015.10:31125729:AAAAA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
8317486507	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3697616415	NC_000015.10:31125730:AAAAA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss82514697	NC_000015.8:29205247:AAAA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3787805377	NC_000015.9:31417932:AAAA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4286255795, ss5297935098, ss5491725826	NC_000015.10:31125729:AAAA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
8317486507	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3697616414	NC_000015.10:31125731:AAAA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5297935100, ss5491725828	NC_000015.10:31125729:AAA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
8317486507	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
8317486507	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3697616413	NC_000015.10:31125733:AA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4286255794, ss5491725825	NC_000015.10:31125729:A:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
8317486507	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3697616412	NC_000015.10:31125734:A:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss95654333	NT_010194.17:2208509:A:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3792823857, ss3797708311, ss5215516728	NC_000015.9:31417932::A	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4286255787, ss5491725827, ss5769122617	NC_000015.10:31125729::A	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
8317486507	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3697616411	NC_000015.10:31125735::A	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5215516730	NC_000015.9:31417932::AA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4286255788, ss5297935096, ss5769122618	NC_000015.10:31125729::AA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
8317486507	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4286255789	NC_000015.10:31125729::AAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
8317486507	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4286255790	NC_000015.10:31125729::AAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
8317486507	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss95654333	NT_010194.17:2208509:A:AAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4286255791	NC_000015.10:31125729::AAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4286255792	NC_000015.10:31125729::AAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4286255793	NC_000015.10:31125729::AAAAAAAAAA	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3223799910	NC_000015.10:31125729:AA:	NC_000015.10:31125729:AAAAAAAAAAAA… NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA

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

No publications for rs59878175

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

rs59878175