Name: rs1162503837
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.

rs1162503837

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:51018001-51018025 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(A)₁₄ / del(A)₁₃ / del(A)₁₁ / d…
del(A)₁₄ / del(A)₁₃ / 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 / dup(A)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₄=0.0000 (0/3042, ALFA)
del(A)₁₃=0.0000 (0/3042, ALFA)
del(A)₁₁=0.0000 (0/3042, ALFA) (+ 17 more)
del(A)₁₀=0.0000 (0/3042, ALFA)
del(A)₉=0.0000 (0/3042, ALFA)
del(A)₈=0.0000 (0/3042, ALFA)
del(A)₇=0.0000 (0/3042, ALFA)
del(A)₆=0.0000 (0/3042, ALFA)
del(A)₅=0.0000 (0/3042, ALFA)
del(A)₄=0.0000 (0/3042, ALFA)
delAAA=0.0000 (0/3042, ALFA)
delAA=0.0000 (0/3042, ALFA)
delA=0.0000 (0/3042, ALFA)
dupA=0.0000 (0/3042, ALFA)
dupAA=0.0000 (0/3042, ALFA)
dupAAA=0.0000 (0/3042, ALFA)
dup(A)₄=0.0000 (0/3042, ALFA)
dup(A)₅=0.0000 (0/3042, ALFA)
dup(A)₆=0.0000 (0/3042, ALFA)
dup(A)₇=0.0000 (0/3042, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: KLK10 : 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	3042	AAAAAAAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	2348	AAAAAAAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	298	AAAAAAAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	8	AAAAAAAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
African American	Sub	290	AAAAAAAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	30	AAAAAAAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	24	AAAAAAAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	6	AAAAAAAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	40	AAAAAAAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	182	AAAAAAAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	38	AAAAAAAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	106	AAAAAAAAAAAAAAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=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	3042	(A)₂₅=1.0000	del(A)₁₄=0.0000, del(A)₁₃=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	2348	(A)₂₅=1.0000	del(A)₁₄=0.0000, del(A)₁₃=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	African	Sub	298	(A)₂₅=1.000	del(A)₁₄=0.000, del(A)₁₃=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	182	(A)₂₅=1.000	del(A)₁₄=0.000, del(A)₁₃=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	106	(A)₂₅=1.000	del(A)₁₄=0.000, del(A)₁₃=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 1	Sub	40	(A)₂₅=1.00	del(A)₁₄=0.00, del(A)₁₃=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	38	(A)₂₅=1.00	del(A)₁₄=0.00, del(A)₁₃=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	30	(A)₂₅=1.00	del(A)₁₄=0.00, del(A)₁₃=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 19	NC_000019.10:g.51018012_51018025del
GRCh38.p14 chr 19	NC_000019.10:g.51018013_51018025del
GRCh38.p14 chr 19	NC_000019.10:g.51018015_51018025del
GRCh38.p14 chr 19	NC_000019.10:g.51018016_51018025del
GRCh38.p14 chr 19	NC_000019.10:g.51018017_51018025del
GRCh38.p14 chr 19	NC_000019.10:g.51018018_51018025del
GRCh38.p14 chr 19	NC_000019.10:g.51018019_51018025del
GRCh38.p14 chr 19	NC_000019.10:g.51018020_51018025del
GRCh38.p14 chr 19	NC_000019.10:g.51018021_51018025del
GRCh38.p14 chr 19	NC_000019.10:g.51018022_51018025del
GRCh38.p14 chr 19	NC_000019.10:g.51018023_51018025del
GRCh38.p14 chr 19	NC_000019.10:g.51018024_51018025del
GRCh38.p14 chr 19	NC_000019.10:g.51018025del
GRCh38.p14 chr 19	NC_000019.10:g.51018025dup
GRCh38.p14 chr 19	NC_000019.10:g.51018024_51018025dup
GRCh38.p14 chr 19	NC_000019.10:g.51018023_51018025dup
GRCh38.p14 chr 19	NC_000019.10:g.51018022_51018025dup
GRCh38.p14 chr 19	NC_000019.10:g.51018021_51018025dup
GRCh38.p14 chr 19	NC_000019.10:g.51018020_51018025dup
GRCh38.p14 chr 19	NC_000019.10:g.51018019_51018025dup
GRCh38.p14 chr 19	NC_000019.10:g.51018018_51018025dup
GRCh38.p14 chr 19	NC_000019.10:g.51018017_51018025dup
GRCh38.p14 chr 19	NC_000019.10:g.51018016_51018025dup
GRCh37.p13 chr 19	NC_000019.9:g.51521268_51521281del
GRCh37.p13 chr 19	NC_000019.9:g.51521269_51521281del
GRCh37.p13 chr 19	NC_000019.9:g.51521271_51521281del
GRCh37.p13 chr 19	NC_000019.9:g.51521272_51521281del
GRCh37.p13 chr 19	NC_000019.9:g.51521273_51521281del
GRCh37.p13 chr 19	NC_000019.9:g.51521274_51521281del
GRCh37.p13 chr 19	NC_000019.9:g.51521275_51521281del
GRCh37.p13 chr 19	NC_000019.9:g.51521276_51521281del
GRCh37.p13 chr 19	NC_000019.9:g.51521277_51521281del
GRCh37.p13 chr 19	NC_000019.9:g.51521278_51521281del
GRCh37.p13 chr 19	NC_000019.9:g.51521279_51521281del
GRCh37.p13 chr 19	NC_000019.9:g.51521280_51521281del
GRCh37.p13 chr 19	NC_000019.9:g.51521281del
GRCh37.p13 chr 19	NC_000019.9:g.51521281dup
GRCh37.p13 chr 19	NC_000019.9:g.51521280_51521281dup
GRCh37.p13 chr 19	NC_000019.9:g.51521279_51521281dup
GRCh37.p13 chr 19	NC_000019.9:g.51521278_51521281dup
GRCh37.p13 chr 19	NC_000019.9:g.51521277_51521281dup
GRCh37.p13 chr 19	NC_000019.9:g.51521276_51521281dup
GRCh37.p13 chr 19	NC_000019.9:g.51521275_51521281dup
GRCh37.p13 chr 19	NC_000019.9:g.51521274_51521281dup
GRCh37.p13 chr 19	NC_000019.9:g.51521273_51521281dup
GRCh37.p13 chr 19	NC_000019.9:g.51521272_51521281dup

Gene: KLK10, kallikrein related peptidase 10 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
KLK10 transcript variant 3	NM_001077500.2:c.89-724_8… NM_001077500.2:c.89-724_89-711del	N/A	Intron Variant
KLK10 transcript variant 1	NM_002776.5:c.89-724_89-7… NM_002776.5:c.89-724_89-711del	N/A	Intron Variant
KLK10 transcript variant 2	NM_145888.3:c.89-724_89-7… NM_145888.3:c.89-724_89-711del	N/A	Intron Variant
KLK10 transcript variant X1	XM_005259061.4:c.89-724_8… XM_005259061.4:c.89-724_89-711del	N/A	Intron Variant
KLK10 transcript variant X3	XM_005259062.4:c.89-724_8… XM_005259062.4:c.89-724_89-711del	N/A	Intron Variant
KLK10 transcript variant X2	XM_006723287.5:c.89-724_8… XM_006723287.5:c.89-724_89-711del	N/A	Intron Variant
KLK10 transcript variant X4	XM_006723289.4:c.89-724_8… XM_006723289.4:c.89-724_89-711del	N/A	Intron Variant
KLK10 transcript variant X5	XM_017026993.3:c.89-724_8… XM_017026993.3:c.89-724_89-711del	N/A	Intron Variant
KLK10 transcript variant X6	XM_047439102.1:c.89-724_8… XM_047439102.1:c.89-724_89-711del	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)₂₅=	del(A)₁₄	del(A)₁₃	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	dup(A)₁₀
GRCh38.p14 chr 19	NC_000019.10:g.51018001_51018025=	NC_000019.10:g.51018012_51018025del	NC_000019.10:g.51018013_51018025del	NC_000019.10:g.51018015_51018025del	NC_000019.10:g.51018016_51018025del	NC_000019.10:g.51018017_51018025del	NC_000019.10:g.51018018_51018025del	NC_000019.10:g.51018019_51018025del	NC_000019.10:g.51018020_51018025del	NC_000019.10:g.51018021_51018025del	NC_000019.10:g.51018022_51018025del	NC_000019.10:g.51018023_51018025del	NC_000019.10:g.51018024_51018025del	NC_000019.10:g.51018025del	NC_000019.10:g.51018025dup	NC_000019.10:g.51018024_51018025dup	NC_000019.10:g.51018023_51018025dup	NC_000019.10:g.51018022_51018025dup	NC_000019.10:g.51018021_51018025dup	NC_000019.10:g.51018020_51018025dup	NC_000019.10:g.51018019_51018025dup	NC_000019.10:g.51018018_51018025dup	NC_000019.10:g.51018017_51018025dup	NC_000019.10:g.51018016_51018025dup
GRCh37.p13 chr 19	NC_000019.9:g.51521257_51521281=	NC_000019.9:g.51521268_51521281del	NC_000019.9:g.51521269_51521281del	NC_000019.9:g.51521271_51521281del	NC_000019.9:g.51521272_51521281del	NC_000019.9:g.51521273_51521281del	NC_000019.9:g.51521274_51521281del	NC_000019.9:g.51521275_51521281del	NC_000019.9:g.51521276_51521281del	NC_000019.9:g.51521277_51521281del	NC_000019.9:g.51521278_51521281del	NC_000019.9:g.51521279_51521281del	NC_000019.9:g.51521280_51521281del	NC_000019.9:g.51521281del	NC_000019.9:g.51521281dup	NC_000019.9:g.51521280_51521281dup	NC_000019.9:g.51521279_51521281dup	NC_000019.9:g.51521278_51521281dup	NC_000019.9:g.51521277_51521281dup	NC_000019.9:g.51521276_51521281dup	NC_000019.9:g.51521275_51521281dup	NC_000019.9:g.51521274_51521281dup	NC_000019.9:g.51521273_51521281dup	NC_000019.9:g.51521272_51521281dup
KLK10 transcript variant 3	NM_001077500.1:c.89-711=	NM_001077500.1:c.89-724_89-711del	NM_001077500.1:c.89-723_89-711del	NM_001077500.1:c.89-721_89-711del	NM_001077500.1:c.89-720_89-711del	NM_001077500.1:c.89-719_89-711del	NM_001077500.1:c.89-718_89-711del	NM_001077500.1:c.89-717_89-711del	NM_001077500.1:c.89-716_89-711del	NM_001077500.1:c.89-715_89-711del	NM_001077500.1:c.89-714_89-711del	NM_001077500.1:c.89-713_89-711del	NM_001077500.1:c.89-712_89-711del	NM_001077500.1:c.89-711del	NM_001077500.1:c.89-711dup	NM_001077500.1:c.89-712_89-711dup	NM_001077500.1:c.89-713_89-711dup	NM_001077500.1:c.89-714_89-711dup	NM_001077500.1:c.89-715_89-711dup	NM_001077500.1:c.89-716_89-711dup	NM_001077500.1:c.89-717_89-711dup	NM_001077500.1:c.89-718_89-711dup	NM_001077500.1:c.89-719_89-711dup	NM_001077500.1:c.89-720_89-711dup
KLK10 transcript variant 3	NM_001077500.2:c.89-711=	NM_001077500.2:c.89-724_89-711del	NM_001077500.2:c.89-723_89-711del	NM_001077500.2:c.89-721_89-711del	NM_001077500.2:c.89-720_89-711del	NM_001077500.2:c.89-719_89-711del	NM_001077500.2:c.89-718_89-711del	NM_001077500.2:c.89-717_89-711del	NM_001077500.2:c.89-716_89-711del	NM_001077500.2:c.89-715_89-711del	NM_001077500.2:c.89-714_89-711del	NM_001077500.2:c.89-713_89-711del	NM_001077500.2:c.89-712_89-711del	NM_001077500.2:c.89-711del	NM_001077500.2:c.89-711dup	NM_001077500.2:c.89-712_89-711dup	NM_001077500.2:c.89-713_89-711dup	NM_001077500.2:c.89-714_89-711dup	NM_001077500.2:c.89-715_89-711dup	NM_001077500.2:c.89-716_89-711dup	NM_001077500.2:c.89-717_89-711dup	NM_001077500.2:c.89-718_89-711dup	NM_001077500.2:c.89-719_89-711dup	NM_001077500.2:c.89-720_89-711dup
KLK10 transcript variant 1	NM_002776.4:c.89-711=	NM_002776.4:c.89-724_89-711del	NM_002776.4:c.89-723_89-711del	NM_002776.4:c.89-721_89-711del	NM_002776.4:c.89-720_89-711del	NM_002776.4:c.89-719_89-711del	NM_002776.4:c.89-718_89-711del	NM_002776.4:c.89-717_89-711del	NM_002776.4:c.89-716_89-711del	NM_002776.4:c.89-715_89-711del	NM_002776.4:c.89-714_89-711del	NM_002776.4:c.89-713_89-711del	NM_002776.4:c.89-712_89-711del	NM_002776.4:c.89-711del	NM_002776.4:c.89-711dup	NM_002776.4:c.89-712_89-711dup	NM_002776.4:c.89-713_89-711dup	NM_002776.4:c.89-714_89-711dup	NM_002776.4:c.89-715_89-711dup	NM_002776.4:c.89-716_89-711dup	NM_002776.4:c.89-717_89-711dup	NM_002776.4:c.89-718_89-711dup	NM_002776.4:c.89-719_89-711dup	NM_002776.4:c.89-720_89-711dup
KLK10 transcript variant 1	NM_002776.5:c.89-711=	NM_002776.5:c.89-724_89-711del	NM_002776.5:c.89-723_89-711del	NM_002776.5:c.89-721_89-711del	NM_002776.5:c.89-720_89-711del	NM_002776.5:c.89-719_89-711del	NM_002776.5:c.89-718_89-711del	NM_002776.5:c.89-717_89-711del	NM_002776.5:c.89-716_89-711del	NM_002776.5:c.89-715_89-711del	NM_002776.5:c.89-714_89-711del	NM_002776.5:c.89-713_89-711del	NM_002776.5:c.89-712_89-711del	NM_002776.5:c.89-711del	NM_002776.5:c.89-711dup	NM_002776.5:c.89-712_89-711dup	NM_002776.5:c.89-713_89-711dup	NM_002776.5:c.89-714_89-711dup	NM_002776.5:c.89-715_89-711dup	NM_002776.5:c.89-716_89-711dup	NM_002776.5:c.89-717_89-711dup	NM_002776.5:c.89-718_89-711dup	NM_002776.5:c.89-719_89-711dup	NM_002776.5:c.89-720_89-711dup
KLK10 transcript variant 2	NM_145888.2:c.89-711=	NM_145888.2:c.89-724_89-711del	NM_145888.2:c.89-723_89-711del	NM_145888.2:c.89-721_89-711del	NM_145888.2:c.89-720_89-711del	NM_145888.2:c.89-719_89-711del	NM_145888.2:c.89-718_89-711del	NM_145888.2:c.89-717_89-711del	NM_145888.2:c.89-716_89-711del	NM_145888.2:c.89-715_89-711del	NM_145888.2:c.89-714_89-711del	NM_145888.2:c.89-713_89-711del	NM_145888.2:c.89-712_89-711del	NM_145888.2:c.89-711del	NM_145888.2:c.89-711dup	NM_145888.2:c.89-712_89-711dup	NM_145888.2:c.89-713_89-711dup	NM_145888.2:c.89-714_89-711dup	NM_145888.2:c.89-715_89-711dup	NM_145888.2:c.89-716_89-711dup	NM_145888.2:c.89-717_89-711dup	NM_145888.2:c.89-718_89-711dup	NM_145888.2:c.89-719_89-711dup	NM_145888.2:c.89-720_89-711dup
KLK10 transcript variant 2	NM_145888.3:c.89-711=	NM_145888.3:c.89-724_89-711del	NM_145888.3:c.89-723_89-711del	NM_145888.3:c.89-721_89-711del	NM_145888.3:c.89-720_89-711del	NM_145888.3:c.89-719_89-711del	NM_145888.3:c.89-718_89-711del	NM_145888.3:c.89-717_89-711del	NM_145888.3:c.89-716_89-711del	NM_145888.3:c.89-715_89-711del	NM_145888.3:c.89-714_89-711del	NM_145888.3:c.89-713_89-711del	NM_145888.3:c.89-712_89-711del	NM_145888.3:c.89-711del	NM_145888.3:c.89-711dup	NM_145888.3:c.89-712_89-711dup	NM_145888.3:c.89-713_89-711dup	NM_145888.3:c.89-714_89-711dup	NM_145888.3:c.89-715_89-711dup	NM_145888.3:c.89-716_89-711dup	NM_145888.3:c.89-717_89-711dup	NM_145888.3:c.89-718_89-711dup	NM_145888.3:c.89-719_89-711dup	NM_145888.3:c.89-720_89-711dup
KLK10 transcript variant X1	XM_005259061.1:c.89-711=	XM_005259061.1:c.89-724_89-711del	XM_005259061.1:c.89-723_89-711del	XM_005259061.1:c.89-721_89-711del	XM_005259061.1:c.89-720_89-711del	XM_005259061.1:c.89-719_89-711del	XM_005259061.1:c.89-718_89-711del	XM_005259061.1:c.89-717_89-711del	XM_005259061.1:c.89-716_89-711del	XM_005259061.1:c.89-715_89-711del	XM_005259061.1:c.89-714_89-711del	XM_005259061.1:c.89-713_89-711del	XM_005259061.1:c.89-712_89-711del	XM_005259061.1:c.89-711del	XM_005259061.1:c.89-711dup	XM_005259061.1:c.89-712_89-711dup	XM_005259061.1:c.89-713_89-711dup	XM_005259061.1:c.89-714_89-711dup	XM_005259061.1:c.89-715_89-711dup	XM_005259061.1:c.89-716_89-711dup	XM_005259061.1:c.89-717_89-711dup	XM_005259061.1:c.89-718_89-711dup	XM_005259061.1:c.89-719_89-711dup	XM_005259061.1:c.89-720_89-711dup
KLK10 transcript variant X1	XM_005259061.4:c.89-711=	XM_005259061.4:c.89-724_89-711del	XM_005259061.4:c.89-723_89-711del	XM_005259061.4:c.89-721_89-711del	XM_005259061.4:c.89-720_89-711del	XM_005259061.4:c.89-719_89-711del	XM_005259061.4:c.89-718_89-711del	XM_005259061.4:c.89-717_89-711del	XM_005259061.4:c.89-716_89-711del	XM_005259061.4:c.89-715_89-711del	XM_005259061.4:c.89-714_89-711del	XM_005259061.4:c.89-713_89-711del	XM_005259061.4:c.89-712_89-711del	XM_005259061.4:c.89-711del	XM_005259061.4:c.89-711dup	XM_005259061.4:c.89-712_89-711dup	XM_005259061.4:c.89-713_89-711dup	XM_005259061.4:c.89-714_89-711dup	XM_005259061.4:c.89-715_89-711dup	XM_005259061.4:c.89-716_89-711dup	XM_005259061.4:c.89-717_89-711dup	XM_005259061.4:c.89-718_89-711dup	XM_005259061.4:c.89-719_89-711dup	XM_005259061.4:c.89-720_89-711dup
KLK10 transcript variant X2	XM_005259062.1:c.89-711=	XM_005259062.1:c.89-724_89-711del	XM_005259062.1:c.89-723_89-711del	XM_005259062.1:c.89-721_89-711del	XM_005259062.1:c.89-720_89-711del	XM_005259062.1:c.89-719_89-711del	XM_005259062.1:c.89-718_89-711del	XM_005259062.1:c.89-717_89-711del	XM_005259062.1:c.89-716_89-711del	XM_005259062.1:c.89-715_89-711del	XM_005259062.1:c.89-714_89-711del	XM_005259062.1:c.89-713_89-711del	XM_005259062.1:c.89-712_89-711del	XM_005259062.1:c.89-711del	XM_005259062.1:c.89-711dup	XM_005259062.1:c.89-712_89-711dup	XM_005259062.1:c.89-713_89-711dup	XM_005259062.1:c.89-714_89-711dup	XM_005259062.1:c.89-715_89-711dup	XM_005259062.1:c.89-716_89-711dup	XM_005259062.1:c.89-717_89-711dup	XM_005259062.1:c.89-718_89-711dup	XM_005259062.1:c.89-719_89-711dup	XM_005259062.1:c.89-720_89-711dup
KLK10 transcript variant X3	XM_005259062.4:c.89-711=	XM_005259062.4:c.89-724_89-711del	XM_005259062.4:c.89-723_89-711del	XM_005259062.4:c.89-721_89-711del	XM_005259062.4:c.89-720_89-711del	XM_005259062.4:c.89-719_89-711del	XM_005259062.4:c.89-718_89-711del	XM_005259062.4:c.89-717_89-711del	XM_005259062.4:c.89-716_89-711del	XM_005259062.4:c.89-715_89-711del	XM_005259062.4:c.89-714_89-711del	XM_005259062.4:c.89-713_89-711del	XM_005259062.4:c.89-712_89-711del	XM_005259062.4:c.89-711del	XM_005259062.4:c.89-711dup	XM_005259062.4:c.89-712_89-711dup	XM_005259062.4:c.89-713_89-711dup	XM_005259062.4:c.89-714_89-711dup	XM_005259062.4:c.89-715_89-711dup	XM_005259062.4:c.89-716_89-711dup	XM_005259062.4:c.89-717_89-711dup	XM_005259062.4:c.89-718_89-711dup	XM_005259062.4:c.89-719_89-711dup	XM_005259062.4:c.89-720_89-711dup
KLK10 transcript variant X2	XM_006723287.5:c.89-711=	XM_006723287.5:c.89-724_89-711del	XM_006723287.5:c.89-723_89-711del	XM_006723287.5:c.89-721_89-711del	XM_006723287.5:c.89-720_89-711del	XM_006723287.5:c.89-719_89-711del	XM_006723287.5:c.89-718_89-711del	XM_006723287.5:c.89-717_89-711del	XM_006723287.5:c.89-716_89-711del	XM_006723287.5:c.89-715_89-711del	XM_006723287.5:c.89-714_89-711del	XM_006723287.5:c.89-713_89-711del	XM_006723287.5:c.89-712_89-711del	XM_006723287.5:c.89-711del	XM_006723287.5:c.89-711dup	XM_006723287.5:c.89-712_89-711dup	XM_006723287.5:c.89-713_89-711dup	XM_006723287.5:c.89-714_89-711dup	XM_006723287.5:c.89-715_89-711dup	XM_006723287.5:c.89-716_89-711dup	XM_006723287.5:c.89-717_89-711dup	XM_006723287.5:c.89-718_89-711dup	XM_006723287.5:c.89-719_89-711dup	XM_006723287.5:c.89-720_89-711dup
KLK10 transcript variant X4	XM_006723289.4:c.89-711=	XM_006723289.4:c.89-724_89-711del	XM_006723289.4:c.89-723_89-711del	XM_006723289.4:c.89-721_89-711del	XM_006723289.4:c.89-720_89-711del	XM_006723289.4:c.89-719_89-711del	XM_006723289.4:c.89-718_89-711del	XM_006723289.4:c.89-717_89-711del	XM_006723289.4:c.89-716_89-711del	XM_006723289.4:c.89-715_89-711del	XM_006723289.4:c.89-714_89-711del	XM_006723289.4:c.89-713_89-711del	XM_006723289.4:c.89-712_89-711del	XM_006723289.4:c.89-711del	XM_006723289.4:c.89-711dup	XM_006723289.4:c.89-712_89-711dup	XM_006723289.4:c.89-713_89-711dup	XM_006723289.4:c.89-714_89-711dup	XM_006723289.4:c.89-715_89-711dup	XM_006723289.4:c.89-716_89-711dup	XM_006723289.4:c.89-717_89-711dup	XM_006723289.4:c.89-718_89-711dup	XM_006723289.4:c.89-719_89-711dup	XM_006723289.4:c.89-720_89-711dup
KLK10 transcript variant X5	XM_017026993.3:c.89-711=	XM_017026993.3:c.89-724_89-711del	XM_017026993.3:c.89-723_89-711del	XM_017026993.3:c.89-721_89-711del	XM_017026993.3:c.89-720_89-711del	XM_017026993.3:c.89-719_89-711del	XM_017026993.3:c.89-718_89-711del	XM_017026993.3:c.89-717_89-711del	XM_017026993.3:c.89-716_89-711del	XM_017026993.3:c.89-715_89-711del	XM_017026993.3:c.89-714_89-711del	XM_017026993.3:c.89-713_89-711del	XM_017026993.3:c.89-712_89-711del	XM_017026993.3:c.89-711del	XM_017026993.3:c.89-711dup	XM_017026993.3:c.89-712_89-711dup	XM_017026993.3:c.89-713_89-711dup	XM_017026993.3:c.89-714_89-711dup	XM_017026993.3:c.89-715_89-711dup	XM_017026993.3:c.89-716_89-711dup	XM_017026993.3:c.89-717_89-711dup	XM_017026993.3:c.89-718_89-711dup	XM_017026993.3:c.89-719_89-711dup	XM_017026993.3:c.89-720_89-711dup
KLK10 transcript variant X6	XM_047439102.1:c.89-711=	XM_047439102.1:c.89-724_89-711del	XM_047439102.1:c.89-723_89-711del	XM_047439102.1:c.89-721_89-711del	XM_047439102.1:c.89-720_89-711del	XM_047439102.1:c.89-719_89-711del	XM_047439102.1:c.89-718_89-711del	XM_047439102.1:c.89-717_89-711del	XM_047439102.1:c.89-716_89-711del	XM_047439102.1:c.89-715_89-711del	XM_047439102.1:c.89-714_89-711del	XM_047439102.1:c.89-713_89-711del	XM_047439102.1:c.89-712_89-711del	XM_047439102.1:c.89-711del	XM_047439102.1:c.89-711dup	XM_047439102.1:c.89-712_89-711dup	XM_047439102.1:c.89-713_89-711dup	XM_047439102.1:c.89-714_89-711dup	XM_047439102.1:c.89-715_89-711dup	XM_047439102.1:c.89-716_89-711dup	XM_047439102.1:c.89-717_89-711dup	XM_047439102.1:c.89-718_89-711dup	XM_047439102.1:c.89-719_89-711dup	XM_047439102.1:c.89-720_89-711dup

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#.

42 SubSNP, 33 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss3017626059	Nov 08, 2017 (151)
2	URBANLAB	ss3650935804	Oct 12, 2018 (152)
3	EVA_DECODE	ss3702945735	Jul 13, 2019 (153)
4	EVA_DECODE	ss3702945736	Jul 13, 2019 (153)
5	EVA_DECODE	ss3702945737	Jul 13, 2019 (153)
6	EVA_DECODE	ss3702945738	Jul 13, 2019 (153)
7	EVA_DECODE	ss3702945739	Jul 13, 2019 (153)
8	EVA	ss3835507087	Apr 27, 2020 (154)
9	GNOMAD	ss4332765729	Apr 27, 2021 (155)
10	GNOMAD	ss4332765730	Apr 27, 2021 (155)
11	GNOMAD	ss4332765731	Apr 27, 2021 (155)
12	GNOMAD	ss4332765732	Apr 27, 2021 (155)
13	GNOMAD	ss4332765733	Apr 27, 2021 (155)
14	GNOMAD	ss4332765734	Apr 27, 2021 (155)
15	GNOMAD	ss4332765735	Apr 27, 2021 (155)
16	GNOMAD	ss4332765736	Apr 27, 2021 (155)
17	GNOMAD	ss4332765737	Apr 27, 2021 (155)
18	GNOMAD	ss4332765739	Apr 27, 2021 (155)
19	GNOMAD	ss4332765740	Apr 27, 2021 (155)
20	GNOMAD	ss4332765741	Apr 27, 2021 (155)
21	GNOMAD	ss4332765742	Apr 27, 2021 (155)
22	GNOMAD	ss4332765743	Apr 27, 2021 (155)
23	GNOMAD	ss4332765744	Apr 27, 2021 (155)
24	GNOMAD	ss4332765745	Apr 27, 2021 (155)
25	GNOMAD	ss4332765746	Apr 27, 2021 (155)
26	GNOMAD	ss4332765747	Apr 27, 2021 (155)
27	GNOMAD	ss4332765748	Apr 27, 2021 (155)
28	GNOMAD	ss4332765749	Apr 27, 2021 (155)
29	TOMMO_GENOMICS	ss5228193173	Apr 27, 2021 (155)
30	TOMMO_GENOMICS	ss5228193174	Apr 27, 2021 (155)
31	TOMMO_GENOMICS	ss5228193175	Apr 27, 2021 (155)
32	TOMMO_GENOMICS	ss5228193176	Apr 27, 2021 (155)
33	TOMMO_GENOMICS	ss5228193177	Apr 27, 2021 (155)
34	TOMMO_GENOMICS	ss5228193178	Apr 27, 2021 (155)
35	1000G_HIGH_COVERAGE	ss5307578422	Oct 13, 2022 (156)
36	HUGCELL_USP	ss5500044724	Oct 13, 2022 (156)
37	TOMMO_GENOMICS	ss5786975590	Oct 13, 2022 (156)
38	TOMMO_GENOMICS	ss5786975591	Oct 13, 2022 (156)
39	TOMMO_GENOMICS	ss5786975592	Oct 13, 2022 (156)
40	TOMMO_GENOMICS	ss5786975593	Oct 13, 2022 (156)
41	TOMMO_GENOMICS	ss5786975594	Oct 13, 2022 (156)
42	TOMMO_GENOMICS	ss5786975595	Oct 13, 2022 (156)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542589293 (NC_000019.10:51018000::A 1483/26492) Row 542589294 (NC_000019.10:51018000::AA 132/26532) Row 542589295 (NC_000019.10:51018000::AAA 441/26558)...	-	Apr 27, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542589293 (NC_000019.10:51018000::A 1483/26492) Row 542589294 (NC_000019.10:51018000::AA 132/26532) Row 542589295 (NC_000019.10:51018000::AAA 441/26558)...	-	Apr 27, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542589293 (NC_000019.10:51018000::A 1483/26492) Row 542589294 (NC_000019.10:51018000::AA 132/26532) Row 542589295 (NC_000019.10:51018000::AAA 441/26558)...	-	Apr 27, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542589293 (NC_000019.10:51018000::A 1483/26492) Row 542589294 (NC_000019.10:51018000::AA 132/26532) Row 542589295 (NC_000019.10:51018000::AAA 441/26558)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542589293 (NC_000019.10:51018000::A 1483/26492) Row 542589294 (NC_000019.10:51018000::AA 132/26532) Row 542589295 (NC_000019.10:51018000::AAA 441/26558)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542589293 (NC_000019.10:51018000::A 1483/26492) Row 542589294 (NC_000019.10:51018000::AA 132/26532) Row 542589295 (NC_000019.10:51018000::AAA 441/26558)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542589293 (NC_000019.10:51018000::A 1483/26492) Row 542589294 (NC_000019.10:51018000::AA 132/26532) Row 542589295 (NC_000019.10:51018000::AAA 441/26558)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542589293 (NC_000019.10:51018000::A 1483/26492) Row 542589294 (NC_000019.10:51018000::AA 132/26532) Row 542589295 (NC_000019.10:51018000::AAA 441/26558)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542589293 (NC_000019.10:51018000::A 1483/26492) Row 542589294 (NC_000019.10:51018000::AA 132/26532) Row 542589295 (NC_000019.10:51018000::AAA 441/26558)...	-	Apr 27, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542589293 (NC_000019.10:51018000::A 1483/26492) Row 542589294 (NC_000019.10:51018000::AA 132/26532) Row 542589295 (NC_000019.10:51018000::AAA 441/26558)...	-	Apr 27, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542589293 (NC_000019.10:51018000::A 1483/26492) Row 542589294 (NC_000019.10:51018000::AA 132/26532) Row 542589295 (NC_000019.10:51018000::AAA 441/26558)...	-	Apr 27, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542589293 (NC_000019.10:51018000::A 1483/26492) Row 542589294 (NC_000019.10:51018000::AA 132/26532) Row 542589295 (NC_000019.10:51018000::AAA 441/26558)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542589293 (NC_000019.10:51018000::A 1483/26492) Row 542589294 (NC_000019.10:51018000::AA 132/26532) Row 542589295 (NC_000019.10:51018000::AAA 441/26558)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542589293 (NC_000019.10:51018000::A 1483/26492) Row 542589294 (NC_000019.10:51018000::AA 132/26532) Row 542589295 (NC_000019.10:51018000::AAA 441/26558)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542589293 (NC_000019.10:51018000::A 1483/26492) Row 542589294 (NC_000019.10:51018000::AA 132/26532) Row 542589295 (NC_000019.10:51018000::AAA 441/26558)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542589293 (NC_000019.10:51018000::A 1483/26492) Row 542589294 (NC_000019.10:51018000::AA 132/26532) Row 542589295 (NC_000019.10:51018000::AAA 441/26558)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542589293 (NC_000019.10:51018000::A 1483/26492) Row 542589294 (NC_000019.10:51018000::AA 132/26532) Row 542589295 (NC_000019.10:51018000::AAA 441/26558)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542589293 (NC_000019.10:51018000::A 1483/26492) Row 542589294 (NC_000019.10:51018000::AA 132/26532) Row 542589295 (NC_000019.10:51018000::AAA 441/26558)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542589293 (NC_000019.10:51018000::A 1483/26492) Row 542589294 (NC_000019.10:51018000::AA 132/26532) Row 542589295 (NC_000019.10:51018000::AAA 441/26558)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542589293 (NC_000019.10:51018000::A 1483/26492) Row 542589294 (NC_000019.10:51018000::AA 132/26532) Row 542589295 (NC_000019.10:51018000::AAA 441/26558)...	-	Apr 27, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 86162480 (NC_000019.9:51521256:AAA: 1888/13872) Row 86162481 (NC_000019.9:51521256::A 228/13872) Row 86162482 (NC_000019.9:51521256::AAAA 980/13872)...	-	Apr 27, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 86162480 (NC_000019.9:51521256:AAA: 1888/13872) Row 86162481 (NC_000019.9:51521256::A 228/13872) Row 86162482 (NC_000019.9:51521256::AAAA 980/13872)...	-	Apr 27, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 86162480 (NC_000019.9:51521256:AAA: 1888/13872) Row 86162481 (NC_000019.9:51521256::A 228/13872) Row 86162482 (NC_000019.9:51521256::AAAA 980/13872)...	-	Apr 27, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 86162480 (NC_000019.9:51521256:AAA: 1888/13872) Row 86162481 (NC_000019.9:51521256::A 228/13872) Row 86162482 (NC_000019.9:51521256::AAAA 980/13872)...	-	Apr 27, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 86162480 (NC_000019.9:51521256:AAA: 1888/13872) Row 86162481 (NC_000019.9:51521256::A 228/13872) Row 86162482 (NC_000019.9:51521256::AAAA 980/13872)...	-	Apr 27, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 86162480 (NC_000019.9:51521256:AAA: 1888/13872) Row 86162481 (NC_000019.9:51521256::A 228/13872) Row 86162482 (NC_000019.9:51521256::AAAA 980/13872)...	-	Apr 27, 2021 (155)
69	14KJPN Submission ignored due to conflicting rows: Row 120812694 (NC_000019.10:51018000:AAA: 3001/20906) Row 120812695 (NC_000019.10:51018000:AA: 1964/20906) Row 120812696 (NC_000019.10:51018000::A 346/20906)...	-	Oct 13, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 120812694 (NC_000019.10:51018000:AAA: 3001/20906) Row 120812695 (NC_000019.10:51018000:AA: 1964/20906) Row 120812696 (NC_000019.10:51018000::A 346/20906)...	-	Oct 13, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 120812694 (NC_000019.10:51018000:AAA: 3001/20906) Row 120812695 (NC_000019.10:51018000:AA: 1964/20906) Row 120812696 (NC_000019.10:51018000::A 346/20906)...	-	Oct 13, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 120812694 (NC_000019.10:51018000:AAA: 3001/20906) Row 120812695 (NC_000019.10:51018000:AA: 1964/20906) Row 120812696 (NC_000019.10:51018000::A 346/20906)...	-	Oct 13, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 120812694 (NC_000019.10:51018000:AAA: 3001/20906) Row 120812695 (NC_000019.10:51018000:AA: 1964/20906) Row 120812696 (NC_000019.10:51018000::A 346/20906)...	-	Oct 13, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 120812694 (NC_000019.10:51018000:AAA: 3001/20906) Row 120812695 (NC_000019.10:51018000:AA: 1964/20906) Row 120812696 (NC_000019.10:51018000::A 346/20906)...	-	Oct 13, 2022 (156)
75	ALFA	NC_000019.10 - 51018001	Apr 27, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
10134933737	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4332765749	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAA:	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
10134933737	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
10134933737	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4332765748	NC_000019.10:51018000:AAAAAAAAAA:	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
10134933737	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4332765747	NC_000019.10:51018000:AAAAAAAAA:	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
10134933737	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4332765746	NC_000019.10:51018000:AAAAAAAA:	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
10134933737	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4332765745	NC_000019.10:51018000:AAAAAAA:	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
10134933737	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4332765744	NC_000019.10:51018000:AAAAAA:	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
10134933737	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4332765743	NC_000019.10:51018000:AAAAA:	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
10134933737	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3702945739, ss4332765742, ss5307578422	NC_000019.10:51018000:AAAA:	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
10134933737	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3017626059, ss5228193173	NC_000019.9:51521256:AAA:	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4332765741, ss5500044724, ss5786975590	NC_000019.10:51018000:AAA:	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
10134933737	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3702945738	NC_000019.10:51018001:AAA:	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5228193176	NC_000019.9:51521256:AA:	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4332765740, ss5786975591	NC_000019.10:51018000:AA:	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
10134933737	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3702945737	NC_000019.10:51018002:AA:	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4332765739	NC_000019.10:51018000:A:	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
10134933737	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5228193174	NC_000019.9:51521256::A	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4332765729, ss5786975592	NC_000019.10:51018000::A	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10134933737	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3702945736	NC_000019.10:51018004::A	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5228193178	NC_000019.9:51521256::AA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4332765730, ss5786975594	NC_000019.10:51018000::AA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10134933737	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4332765731	NC_000019.10:51018000::AAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10134933737	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3835507087, ss5228193175	NC_000019.9:51521256::AAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4332765732, ss5786975593	NC_000019.10:51018000::AAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10134933737	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3702945735	NC_000019.10:51018004::AAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3650935804	NC_000019.10:51018023::AAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5228193177	NC_000019.9:51521256::AAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4332765733, ss5786975595	NC_000019.10:51018000::AAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10134933737	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4332765734	NC_000019.10:51018000::AAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10134933737	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10134933737	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4332765735	NC_000019.10:51018000::AAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4332765736	NC_000019.10:51018000::AAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4332765737	NC_000019.10:51018000::AAAAAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3295592081	NC_000019.10:51018000::AAAAAAA	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ss3295592092	NC_000019.10:51018000:AAAAAAAAAAA:	NC_000019.10:51018000:AAAAAAAAAAAA… NC_000019.10:51018000:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA

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

No publications for rs1162503837

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

rs1162503837