Name: rs1170709894
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.

rs1170709894

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:42771954-42771978 (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)₁₇ / del(A)₁₅ / del(A)₁₃ / d…
del(A)₁₇ / 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)₈ / dup(A)₉ / dup(A)₂₁ / ins(A)₂₉
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₇=0.0000 (0/9682, ALFA)
del(A)₁₅=0.0000 (0/9682, ALFA)
del(A)₁₃=0.0000 (0/9682, ALFA) (+ 16 more)
del(A)₁₂=0.0000 (0/9682, ALFA)
del(A)₁₁=0.0000 (0/9682, ALFA)
del(A)₁₀=0.0000 (0/9682, ALFA)
del(A)₉=0.0000 (0/9682, ALFA)
del(A)₈=0.0000 (0/9682, ALFA)
del(A)₇=0.0000 (0/9682, ALFA)
del(A)₆=0.0000 (0/9682, ALFA)
del(A)₅=0.0000 (0/9682, ALFA)
del(A)₄=0.0000 (0/9682, ALFA)
delAAA=0.0000 (0/9682, ALFA)
delAA=0.0000 (0/9682, ALFA)
delA=0.0000 (0/9682, ALFA)
dupA=0.0000 (0/9682, ALFA)
dupAA=0.0000 (0/9682, ALFA)
dupAAA=0.0000 (0/9682, ALFA)
dup(A)₄=0.0000 (0/9682, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: VPS25 : 2KB Upstream 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	9682	AAAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	7430	AAAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	1040	AAAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	28	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	1012	AAAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	100	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	78	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	22	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	122	AAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Latin American 2	Sub	562	AAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	76	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	352	AAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	9682	(A)₂₅=1.0000	del(A)₁₇=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	7430	(A)₂₅=1.0000	del(A)₁₇=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	1040	(A)₂₅=1.0000	del(A)₁₇=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	Latin American 2	Sub	562	(A)₂₅=1.000	del(A)₁₇=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	352	(A)₂₅=1.000	del(A)₁₇=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	122	(A)₂₅=1.000	del(A)₁₇=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	Asian	Sub	100	(A)₂₅=1.00	del(A)₁₇=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	76	(A)₂₅=1.00	del(A)₁₇=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

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 17	NC_000017.11:g.42771962_42771978del
GRCh38.p14 chr 17	NC_000017.11:g.42771964_42771978del
GRCh38.p14 chr 17	NC_000017.11:g.42771966_42771978del
GRCh38.p14 chr 17	NC_000017.11:g.42771967_42771978del
GRCh38.p14 chr 17	NC_000017.11:g.42771968_42771978del
GRCh38.p14 chr 17	NC_000017.11:g.42771969_42771978del
GRCh38.p14 chr 17	NC_000017.11:g.42771970_42771978del
GRCh38.p14 chr 17	NC_000017.11:g.42771971_42771978del
GRCh38.p14 chr 17	NC_000017.11:g.42771972_42771978del
GRCh38.p14 chr 17	NC_000017.11:g.42771973_42771978del
GRCh38.p14 chr 17	NC_000017.11:g.42771974_42771978del
GRCh38.p14 chr 17	NC_000017.11:g.42771975_42771978del
GRCh38.p14 chr 17	NC_000017.11:g.42771976_42771978del
GRCh38.p14 chr 17	NC_000017.11:g.42771977_42771978del
GRCh38.p14 chr 17	NC_000017.11:g.42771978del
GRCh38.p14 chr 17	NC_000017.11:g.42771978dup
GRCh38.p14 chr 17	NC_000017.11:g.42771977_42771978dup
GRCh38.p14 chr 17	NC_000017.11:g.42771976_42771978dup
GRCh38.p14 chr 17	NC_000017.11:g.42771975_42771978dup
GRCh38.p14 chr 17	NC_000017.11:g.42771974_42771978dup
GRCh38.p14 chr 17	NC_000017.11:g.42771973_42771978dup
GRCh38.p14 chr 17	NC_000017.11:g.42771971_42771978dup
GRCh38.p14 chr 17	NC_000017.11:g.42771970_42771978dup
GRCh38.p14 chr 17	NC_000017.11:g.42771958_42771978dup
GRCh38.p14 chr 17	NC_000017.11:g.42771978_42771979insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 17	NC_000017.10:g.40923980_40923996del
GRCh37.p13 chr 17	NC_000017.10:g.40923982_40923996del
GRCh37.p13 chr 17	NC_000017.10:g.40923984_40923996del
GRCh37.p13 chr 17	NC_000017.10:g.40923985_40923996del
GRCh37.p13 chr 17	NC_000017.10:g.40923986_40923996del
GRCh37.p13 chr 17	NC_000017.10:g.40923987_40923996del
GRCh37.p13 chr 17	NC_000017.10:g.40923988_40923996del
GRCh37.p13 chr 17	NC_000017.10:g.40923989_40923996del
GRCh37.p13 chr 17	NC_000017.10:g.40923990_40923996del
GRCh37.p13 chr 17	NC_000017.10:g.40923991_40923996del
GRCh37.p13 chr 17	NC_000017.10:g.40923992_40923996del
GRCh37.p13 chr 17	NC_000017.10:g.40923993_40923996del
GRCh37.p13 chr 17	NC_000017.10:g.40923994_40923996del
GRCh37.p13 chr 17	NC_000017.10:g.40923995_40923996del
GRCh37.p13 chr 17	NC_000017.10:g.40923996del
GRCh37.p13 chr 17	NC_000017.10:g.40923996dup
GRCh37.p13 chr 17	NC_000017.10:g.40923995_40923996dup
GRCh37.p13 chr 17	NC_000017.10:g.40923994_40923996dup
GRCh37.p13 chr 17	NC_000017.10:g.40923993_40923996dup
GRCh37.p13 chr 17	NC_000017.10:g.40923992_40923996dup
GRCh37.p13 chr 17	NC_000017.10:g.40923991_40923996dup
GRCh37.p13 chr 17	NC_000017.10:g.40923989_40923996dup
GRCh37.p13 chr 17	NC_000017.10:g.40923988_40923996dup
GRCh37.p13 chr 17	NC_000017.10:g.40923976_40923996dup
GRCh37.p13 chr 17	NC_000017.10:g.40923996_40923997insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: VPS25, vacuolar protein sorting 25 homolog (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
VPS25 transcript	NM_032353.4:c.	N/A	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)₂₅=	del(A)₁₇	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)₈	dup(A)₉	dup(A)₂₁	ins(A)₂₉
GRCh38.p14 chr 17	NC_000017.11:g.42771954_42771978=	NC_000017.11:g.42771962_42771978del	NC_000017.11:g.42771964_42771978del	NC_000017.11:g.42771966_42771978del	NC_000017.11:g.42771967_42771978del	NC_000017.11:g.42771968_42771978del	NC_000017.11:g.42771969_42771978del	NC_000017.11:g.42771970_42771978del	NC_000017.11:g.42771971_42771978del	NC_000017.11:g.42771972_42771978del	NC_000017.11:g.42771973_42771978del	NC_000017.11:g.42771974_42771978del	NC_000017.11:g.42771975_42771978del	NC_000017.11:g.42771976_42771978del	NC_000017.11:g.42771977_42771978del	NC_000017.11:g.42771978del	NC_000017.11:g.42771978dup	NC_000017.11:g.42771977_42771978dup	NC_000017.11:g.42771976_42771978dup	NC_000017.11:g.42771975_42771978dup	NC_000017.11:g.42771974_42771978dup	NC_000017.11:g.42771973_42771978dup	NC_000017.11:g.42771971_42771978dup	NC_000017.11:g.42771970_42771978dup	NC_000017.11:g.42771958_42771978dup	NC_000017.11:g.42771978_42771979insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 17	NC_000017.10:g.40923972_40923996=	NC_000017.10:g.40923980_40923996del	NC_000017.10:g.40923982_40923996del	NC_000017.10:g.40923984_40923996del	NC_000017.10:g.40923985_40923996del	NC_000017.10:g.40923986_40923996del	NC_000017.10:g.40923987_40923996del	NC_000017.10:g.40923988_40923996del	NC_000017.10:g.40923989_40923996del	NC_000017.10:g.40923990_40923996del	NC_000017.10:g.40923991_40923996del	NC_000017.10:g.40923992_40923996del	NC_000017.10:g.40923993_40923996del	NC_000017.10:g.40923994_40923996del	NC_000017.10:g.40923995_40923996del	NC_000017.10:g.40923996del	NC_000017.10:g.40923996dup	NC_000017.10:g.40923995_40923996dup	NC_000017.10:g.40923994_40923996dup	NC_000017.10:g.40923993_40923996dup	NC_000017.10:g.40923992_40923996dup	NC_000017.10:g.40923991_40923996dup	NC_000017.10:g.40923989_40923996dup	NC_000017.10:g.40923988_40923996dup	NC_000017.10:g.40923976_40923996dup	NC_000017.10:g.40923996_40923997insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

48 SubSNP, 36 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	MCHAISSO	ss3065650697	Jan 10, 2018 (151)
2	EVA	ss3834868866	Apr 27, 2020 (154)
3	GNOMAD	ss4311649512	Apr 27, 2021 (155)
4	GNOMAD	ss4311649513	Apr 27, 2021 (155)
5	GNOMAD	ss4311649514	Apr 27, 2021 (155)
6	GNOMAD	ss4311649515	Apr 27, 2021 (155)
7	GNOMAD	ss4311649516	Apr 27, 2021 (155)
8	GNOMAD	ss4311649517	Apr 27, 2021 (155)
9	GNOMAD	ss4311649518	Apr 27, 2021 (155)
10	GNOMAD	ss4311649519	Apr 27, 2021 (155)
11	GNOMAD	ss4311649520	Apr 27, 2021 (155)
12	GNOMAD	ss4311649521	Apr 27, 2021 (155)
13	GNOMAD	ss4311649523	Apr 27, 2021 (155)
14	GNOMAD	ss4311649524	Apr 27, 2021 (155)
15	GNOMAD	ss4311649525	Apr 27, 2021 (155)
16	GNOMAD	ss4311649526	Apr 27, 2021 (155)
17	GNOMAD	ss4311649527	Apr 27, 2021 (155)
18	GNOMAD	ss4311649528	Apr 27, 2021 (155)
19	GNOMAD	ss4311649529	Apr 27, 2021 (155)
20	GNOMAD	ss4311649530	Apr 27, 2021 (155)
21	GNOMAD	ss4311649531	Apr 27, 2021 (155)
22	GNOMAD	ss4311649532	Apr 27, 2021 (155)
23	GNOMAD	ss4311649533	Apr 27, 2021 (155)
24	GNOMAD	ss4311649534	Apr 27, 2021 (155)
25	GNOMAD	ss4311649535	Apr 27, 2021 (155)
26	GNOMAD	ss4311649536	Apr 27, 2021 (155)
27	GNOMAD	ss4311649537	Apr 27, 2021 (155)
28	TOPMED	ss5036064669	Apr 27, 2021 (155)
29	TOPMED	ss5036064670	Apr 27, 2021 (155)
30	TOMMO_GENOMICS	ss5222425441	Apr 27, 2021 (155)
31	TOMMO_GENOMICS	ss5222425442	Apr 27, 2021 (155)
32	TOMMO_GENOMICS	ss5222425443	Apr 27, 2021 (155)
33	TOMMO_GENOMICS	ss5222425444	Apr 27, 2021 (155)
34	1000G_HIGH_COVERAGE	ss5303141119	Oct 16, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5303141120	Oct 16, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5303141121	Oct 16, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5303141122	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5496196331	Oct 16, 2022 (156)
39	HUGCELL_USP	ss5496196332	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5496196333	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5496196334	Oct 16, 2022 (156)
42	HUGCELL_USP	ss5496196335	Oct 16, 2022 (156)
43	HUGCELL_USP	ss5496196336	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5778636756	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5778636757	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5778636758	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5778636759	Oct 16, 2022 (156)
48	EVA	ss5980967314	Oct 16, 2022 (156)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507307181 (NC_000017.11:42771953::A 1374/31940) Row 507307182 (NC_000017.11:42771953::AA 375/31872) Row 507307183 (NC_000017.11:42771953::AAA 301/29668)...	-	Apr 27, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 80394748 (NC_000017.10:40923971::A 575/15872) Row 80394749 (NC_000017.10:40923971::AAA 79/15872) Row 80394750 (NC_000017.10:40923971:AAAAAAAAAAA: 7/15872)...	-	Apr 27, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 80394748 (NC_000017.10:40923971::A 575/15872) Row 80394749 (NC_000017.10:40923971::AAA 79/15872) Row 80394750 (NC_000017.10:40923971:AAAAAAAAAAA: 7/15872)...	-	Apr 27, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 80394748 (NC_000017.10:40923971::A 575/15872) Row 80394749 (NC_000017.10:40923971::AAA 79/15872) Row 80394750 (NC_000017.10:40923971:AAAAAAAAAAA: 7/15872)...	-	Apr 27, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 80394748 (NC_000017.10:40923971::A 575/15872) Row 80394749 (NC_000017.10:40923971::AAA 79/15872) Row 80394750 (NC_000017.10:40923971:AAAAAAAAAAA: 7/15872)...	-	Apr 27, 2021 (155)
78	14KJPN Submission ignored due to conflicting rows: Row 112473860 (NC_000017.11:42771953::A 976/24666) Row 112473861 (NC_000017.11:42771953::AAA 95/24666) Row 112473862 (NC_000017.11:42771953:AAAAAAAAAAA: 16/24666)...	-	Oct 16, 2022 (156)
79	14KJPN Submission ignored due to conflicting rows: Row 112473860 (NC_000017.11:42771953::A 976/24666) Row 112473861 (NC_000017.11:42771953::AAA 95/24666) Row 112473862 (NC_000017.11:42771953:AAAAAAAAAAA: 16/24666)...	-	Oct 16, 2022 (156)
80	14KJPN Submission ignored due to conflicting rows: Row 112473860 (NC_000017.11:42771953::A 976/24666) Row 112473861 (NC_000017.11:42771953::AAA 95/24666) Row 112473862 (NC_000017.11:42771953:AAAAAAAAAAA: 16/24666)...	-	Oct 16, 2022 (156)
81	14KJPN Submission ignored due to conflicting rows: Row 112473860 (NC_000017.11:42771953::A 976/24666) Row 112473861 (NC_000017.11:42771953::AAA 95/24666) Row 112473862 (NC_000017.11:42771953:AAAAAAAAAAA: 16/24666)...	-	Oct 16, 2022 (156)
82	TopMed Submission ignored due to conflicting rows: Row 251610331 (NC_000017.11:42771953:AAAAAAAAAAA: 51/264690) Row 251610332 (NC_000017.11:42771953:AAAAAAAAAAAAAAAAA: 2/264690)	-	Apr 27, 2021 (155)
83	TopMed Submission ignored due to conflicting rows: Row 251610331 (NC_000017.11:42771953:AAAAAAAAAAA: 51/264690) Row 251610332 (NC_000017.11:42771953:AAAAAAAAAAAAAAAAA: 2/264690)	-	Apr 27, 2021 (155)
84	ALFA	NC_000017.11 - 42771954	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
ss4311649537, ss5036064670	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAA:	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
6345933639	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
ss4311649536	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAA:	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
6345933639	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4311649535	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAA:	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
6345933639	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4311649534	NC_000017.11:42771953:AAAAAAAAAAAA:	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
6345933639	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5222425443	NC_000017.10:40923971:AAAAAAAAAAA:	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4311649533, ss5036064669, ss5778636758	NC_000017.11:42771953:AAAAAAAAAAA:	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
6345933639	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4311649532	NC_000017.11:42771953:AAAAAAAAAA:	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
6345933639	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4311649531	NC_000017.11:42771953:AAAAAAAAA:	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
6345933639	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4311649530	NC_000017.11:42771953:AAAAAAAA:	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
6345933639	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4311649529	NC_000017.11:42771953:AAAAAAA:	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
6345933639	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4311649528	NC_000017.11:42771953:AAAAAA:	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
6345933639	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5980967314	NC_000017.10:40923971:AAAAA:	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA
ss4311649527	NC_000017.11:42771953:AAAAA:	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
6345933639	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4311649526	NC_000017.11:42771953:AAAA:	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
6345933639	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4311649525, ss5303141119, ss5496196336	NC_000017.11:42771953:AAA:	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
6345933639	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4311649524, ss5303141120, ss5496196335	NC_000017.11:42771953:AA:	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
6345933639	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3834868866	NC_000017.10:40923971:A:	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4311649523, ss5303141121, ss5496196331	NC_000017.11:42771953:A:	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
6345933639	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5222425441	NC_000017.10:40923971::A	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4311649512, ss5496196332, ss5778636756	NC_000017.11:42771953::A	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
6345933639	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5222425444	NC_000017.10:40923971::AA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4311649513, ss5303141122, ss5496196333, ss5778636759	NC_000017.11:42771953::AA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
6345933639	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5222425442	NC_000017.10:40923971::AAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3065650697, ss4311649514, ss5496196334, ss5778636757	NC_000017.11:42771953::AAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
6345933639	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4311649515	NC_000017.11:42771953::AAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
6345933639	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4311649516	NC_000017.11:42771953::AAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4311649517	NC_000017.11:42771953::AAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4311649518	NC_000017.11:42771953::AAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4311649519	NC_000017.11:42771953::AAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4311649520	NC_000017.11:42771953::AAAAAAAAAAA… NC_000017.11:42771953::AAAAAAAAAAAAAAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4311649521	NC_000017.11:42771953::AAAAAAAAAAA… NC_000017.11:42771953::AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000017.11:42771953:AAAAAAAAAAAA… NC_000017.11:42771953:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

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

No publications for rs1170709894

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

rs1170709894