Name: rs5865886
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.

rs5865886

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:10249262-10249282 (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)₁₂ / del(A)₁₁ / del(A)₉ / de…
del(A)₁₂ / del(A)₁₁ / del(A)₉ / 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)₈
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₂=0.0000 (0/2508, ALFA)
del(A)₁₁=0.0000 (0/2508, ALFA)
del(A)₉=0.0000 (0/2508, ALFA) (+ 11 more)
del(A)₇=0.0000 (0/2508, ALFA)
del(A)₆=0.0000 (0/2508, ALFA)
del(A)₅=0.0000 (0/2508, ALFA)
del(A)₄=0.0000 (0/2508, ALFA)
delAAA=0.0000 (0/2508, ALFA)
delAA=0.0000 (0/2508, ALFA)
delA=0.0000 (0/2508, ALFA)
dupA=0.0000 (0/2508, ALFA)
dupAA=0.0000 (0/2508, ALFA)
dupAAA=0.0000 (0/2508, ALFA)
dup(A)₅=0.0000 (0/2508, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ATPSCKMT : Intron Variant
CCT5 : 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	2508	AAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	906	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African	Sub	1178	AAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	42	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	1136	AAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	94	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	72	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	22	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	24	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	180	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	22	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	104	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=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	2508	(A)₂₁=1.0000	del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₉=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	African	Sub	1178	(A)₂₁=1.0000	del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₉=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	European	Sub	906	(A)₂₁=1.000	del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₉=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	180	(A)₂₁=1.000	del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₉=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Other	Sub	104	(A)₂₁=1.000	del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₉=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Asian	Sub	94	(A)₂₁=1.00	del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₉=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	24	(A)₂₁=1.00	del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₉=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	22	(A)₂₁=1.00	del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₉=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₅=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 5	NC_000005.10:g.10249271_10249282del
GRCh38.p14 chr 5	NC_000005.10:g.10249272_10249282del
GRCh38.p14 chr 5	NC_000005.10:g.10249274_10249282del
GRCh38.p14 chr 5	NC_000005.10:g.10249276_10249282del
GRCh38.p14 chr 5	NC_000005.10:g.10249277_10249282del
GRCh38.p14 chr 5	NC_000005.10:g.10249278_10249282del
GRCh38.p14 chr 5	NC_000005.10:g.10249279_10249282del
GRCh38.p14 chr 5	NC_000005.10:g.10249280_10249282del
GRCh38.p14 chr 5	NC_000005.10:g.10249281_10249282del
GRCh38.p14 chr 5	NC_000005.10:g.10249282del
GRCh38.p14 chr 5	NC_000005.10:g.10249282dup
GRCh38.p14 chr 5	NC_000005.10:g.10249281_10249282dup
GRCh38.p14 chr 5	NC_000005.10:g.10249280_10249282dup
GRCh38.p14 chr 5	NC_000005.10:g.10249279_10249282dup
GRCh38.p14 chr 5	NC_000005.10:g.10249278_10249282dup
GRCh38.p14 chr 5	NC_000005.10:g.10249275_10249282dup
GRCh37.p13 chr 5	NC_000005.9:g.10249383_10249394del
GRCh37.p13 chr 5	NC_000005.9:g.10249384_10249394del
GRCh37.p13 chr 5	NC_000005.9:g.10249386_10249394del
GRCh37.p13 chr 5	NC_000005.9:g.10249388_10249394del
GRCh37.p13 chr 5	NC_000005.9:g.10249389_10249394del
GRCh37.p13 chr 5	NC_000005.9:g.10249390_10249394del
GRCh37.p13 chr 5	NC_000005.9:g.10249391_10249394del
GRCh37.p13 chr 5	NC_000005.9:g.10249392_10249394del
GRCh37.p13 chr 5	NC_000005.9:g.10249393_10249394del
GRCh37.p13 chr 5	NC_000005.9:g.10249394del
GRCh37.p13 chr 5	NC_000005.9:g.10249394dup
GRCh37.p13 chr 5	NC_000005.9:g.10249393_10249394dup
GRCh37.p13 chr 5	NC_000005.9:g.10249392_10249394dup
GRCh37.p13 chr 5	NC_000005.9:g.10249391_10249394dup
GRCh37.p13 chr 5	NC_000005.9:g.10249390_10249394dup
GRCh37.p13 chr 5	NC_000005.9:g.10249387_10249394dup
CCT5 RefSeqGene (LRG_361)	NG_012160.1:g.4102_4113del
CCT5 RefSeqGene (LRG_361)	NG_012160.1:g.4103_4113del
CCT5 RefSeqGene (LRG_361)	NG_012160.1:g.4105_4113del
CCT5 RefSeqGene (LRG_361)	NG_012160.1:g.4107_4113del
CCT5 RefSeqGene (LRG_361)	NG_012160.1:g.4108_4113del
CCT5 RefSeqGene (LRG_361)	NG_012160.1:g.4109_4113del
CCT5 RefSeqGene (LRG_361)	NG_012160.1:g.4110_4113del
CCT5 RefSeqGene (LRG_361)	NG_012160.1:g.4111_4113del
CCT5 RefSeqGene (LRG_361)	NG_012160.1:g.4112_4113del
CCT5 RefSeqGene (LRG_361)	NG_012160.1:g.4113del
CCT5 RefSeqGene (LRG_361)	NG_012160.1:g.4113dup
CCT5 RefSeqGene (LRG_361)	NG_012160.1:g.4112_4113dup
CCT5 RefSeqGene (LRG_361)	NG_012160.1:g.4111_4113dup
CCT5 RefSeqGene (LRG_361)	NG_012160.1:g.4110_4113dup
CCT5 RefSeqGene (LRG_361)	NG_012160.1:g.4109_4113dup
CCT5 RefSeqGene (LRG_361)	NG_012160.1:g.4106_4113dup

Gene: ATPSCKMT, ATP synthase c subunit lysine N-methyltransferase (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ATPSCKMT transcript variant 2	NM_001258388.2:c.16+585_1… NM_001258388.2:c.16+585_16+596del	N/A	Intron Variant
ATPSCKMT transcript variant 3	NM_001258389.2:c.16+585_1… NM_001258389.2:c.16+585_16+596del	N/A	Intron Variant
ATPSCKMT transcript variant 1	NM_199133.4:c.16+585_16+5… NM_199133.4:c.16+585_16+596del	N/A	Intron Variant
ATPSCKMT transcript variant 4	NR_047668.2:n.	N/A	Intron Variant
ATPSCKMT transcript variant 5	NR_047669.2:n.	N/A	Intron Variant
ATPSCKMT transcript variant 6	NR_047670.2:n.	N/A	Intron Variant
ATPSCKMT transcript variant X2	XM_011513964.2:c.16+585_1… XM_011513964.2:c.16+585_16+596del	N/A	Intron Variant
ATPSCKMT transcript variant X1	XM_047416713.1:c.16+585_1… XM_047416713.1:c.16+585_16+596del	N/A	Intron Variant

Gene: CCT5, chaperonin containing TCP1 subunit 5 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
CCT5 transcript variant 2	NM_001306153.1:c.	N/A	Upstream Transcript Variant
CCT5 transcript variant 3	NM_001306154.2:c.	N/A	Upstream Transcript Variant
CCT5 transcript variant 4	NM_001306155.2:c.	N/A	Upstream Transcript Variant
CCT5 transcript variant 5	NM_001306156.2:c.	N/A	Upstream Transcript Variant
CCT5 transcript variant 1	NM_012073.5: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)₂₁=	del(A)₁₂	del(A)₁₁	del(A)₉	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)₈
GRCh38.p14 chr 5	NC_000005.10:g.10249262_10249282=	NC_000005.10:g.10249271_10249282del	NC_000005.10:g.10249272_10249282del	NC_000005.10:g.10249274_10249282del	NC_000005.10:g.10249276_10249282del	NC_000005.10:g.10249277_10249282del	NC_000005.10:g.10249278_10249282del	NC_000005.10:g.10249279_10249282del	NC_000005.10:g.10249280_10249282del	NC_000005.10:g.10249281_10249282del	NC_000005.10:g.10249282del	NC_000005.10:g.10249282dup	NC_000005.10:g.10249281_10249282dup	NC_000005.10:g.10249280_10249282dup	NC_000005.10:g.10249279_10249282dup	NC_000005.10:g.10249278_10249282dup	NC_000005.10:g.10249275_10249282dup
GRCh37.p13 chr 5	NC_000005.9:g.10249374_10249394=	NC_000005.9:g.10249383_10249394del	NC_000005.9:g.10249384_10249394del	NC_000005.9:g.10249386_10249394del	NC_000005.9:g.10249388_10249394del	NC_000005.9:g.10249389_10249394del	NC_000005.9:g.10249390_10249394del	NC_000005.9:g.10249391_10249394del	NC_000005.9:g.10249392_10249394del	NC_000005.9:g.10249393_10249394del	NC_000005.9:g.10249394del	NC_000005.9:g.10249394dup	NC_000005.9:g.10249393_10249394dup	NC_000005.9:g.10249392_10249394dup	NC_000005.9:g.10249391_10249394dup	NC_000005.9:g.10249390_10249394dup	NC_000005.9:g.10249387_10249394dup
CCT5 RefSeqGene (LRG_361)	NG_012160.1:g.4093_4113=	NG_012160.1:g.4102_4113del	NG_012160.1:g.4103_4113del	NG_012160.1:g.4105_4113del	NG_012160.1:g.4107_4113del	NG_012160.1:g.4108_4113del	NG_012160.1:g.4109_4113del	NG_012160.1:g.4110_4113del	NG_012160.1:g.4111_4113del	NG_012160.1:g.4112_4113del	NG_012160.1:g.4113del	NG_012160.1:g.4113dup	NG_012160.1:g.4112_4113dup	NG_012160.1:g.4111_4113dup	NG_012160.1:g.4110_4113dup	NG_012160.1:g.4109_4113dup	NG_012160.1:g.4106_4113dup
ATPSCKMT transcript variant 2	NM_001258388.1:c.16+596=	NM_001258388.1:c.16+585_16+596del	NM_001258388.1:c.16+586_16+596del	NM_001258388.1:c.16+588_16+596del	NM_001258388.1:c.16+590_16+596del	NM_001258388.1:c.16+591_16+596del	NM_001258388.1:c.16+592_16+596del	NM_001258388.1:c.16+593_16+596del	NM_001258388.1:c.16+594_16+596del	NM_001258388.1:c.16+595_16+596del	NM_001258388.1:c.16+596del	NM_001258388.1:c.16+596dup	NM_001258388.1:c.16+595_16+596dup	NM_001258388.1:c.16+594_16+596dup	NM_001258388.1:c.16+593_16+596dup	NM_001258388.1:c.16+592_16+596dup	NM_001258388.1:c.16+589_16+596dup
ATPSCKMT transcript variant 2	NM_001258388.2:c.16+596=	NM_001258388.2:c.16+585_16+596del	NM_001258388.2:c.16+586_16+596del	NM_001258388.2:c.16+588_16+596del	NM_001258388.2:c.16+590_16+596del	NM_001258388.2:c.16+591_16+596del	NM_001258388.2:c.16+592_16+596del	NM_001258388.2:c.16+593_16+596del	NM_001258388.2:c.16+594_16+596del	NM_001258388.2:c.16+595_16+596del	NM_001258388.2:c.16+596del	NM_001258388.2:c.16+596dup	NM_001258388.2:c.16+595_16+596dup	NM_001258388.2:c.16+594_16+596dup	NM_001258388.2:c.16+593_16+596dup	NM_001258388.2:c.16+592_16+596dup	NM_001258388.2:c.16+589_16+596dup
ATPSCKMT transcript variant 3	NM_001258389.1:c.16+596=	NM_001258389.1:c.16+585_16+596del	NM_001258389.1:c.16+586_16+596del	NM_001258389.1:c.16+588_16+596del	NM_001258389.1:c.16+590_16+596del	NM_001258389.1:c.16+591_16+596del	NM_001258389.1:c.16+592_16+596del	NM_001258389.1:c.16+593_16+596del	NM_001258389.1:c.16+594_16+596del	NM_001258389.1:c.16+595_16+596del	NM_001258389.1:c.16+596del	NM_001258389.1:c.16+596dup	NM_001258389.1:c.16+595_16+596dup	NM_001258389.1:c.16+594_16+596dup	NM_001258389.1:c.16+593_16+596dup	NM_001258389.1:c.16+592_16+596dup	NM_001258389.1:c.16+589_16+596dup
ATPSCKMT transcript variant 3	NM_001258389.2:c.16+596=	NM_001258389.2:c.16+585_16+596del	NM_001258389.2:c.16+586_16+596del	NM_001258389.2:c.16+588_16+596del	NM_001258389.2:c.16+590_16+596del	NM_001258389.2:c.16+591_16+596del	NM_001258389.2:c.16+592_16+596del	NM_001258389.2:c.16+593_16+596del	NM_001258389.2:c.16+594_16+596del	NM_001258389.2:c.16+595_16+596del	NM_001258389.2:c.16+596del	NM_001258389.2:c.16+596dup	NM_001258389.2:c.16+595_16+596dup	NM_001258389.2:c.16+594_16+596dup	NM_001258389.2:c.16+593_16+596dup	NM_001258389.2:c.16+592_16+596dup	NM_001258389.2:c.16+589_16+596dup
FAM173B transcript variant 1	NM_199133.3:c.16+596=	NM_199133.3:c.16+585_16+596del	NM_199133.3:c.16+586_16+596del	NM_199133.3:c.16+588_16+596del	NM_199133.3:c.16+590_16+596del	NM_199133.3:c.16+591_16+596del	NM_199133.3:c.16+592_16+596del	NM_199133.3:c.16+593_16+596del	NM_199133.3:c.16+594_16+596del	NM_199133.3:c.16+595_16+596del	NM_199133.3:c.16+596del	NM_199133.3:c.16+596dup	NM_199133.3:c.16+595_16+596dup	NM_199133.3:c.16+594_16+596dup	NM_199133.3:c.16+593_16+596dup	NM_199133.3:c.16+592_16+596dup	NM_199133.3:c.16+589_16+596dup
ATPSCKMT transcript variant 1	NM_199133.4:c.16+596=	NM_199133.4:c.16+585_16+596del	NM_199133.4:c.16+586_16+596del	NM_199133.4:c.16+588_16+596del	NM_199133.4:c.16+590_16+596del	NM_199133.4:c.16+591_16+596del	NM_199133.4:c.16+592_16+596del	NM_199133.4:c.16+593_16+596del	NM_199133.4:c.16+594_16+596del	NM_199133.4:c.16+595_16+596del	NM_199133.4:c.16+596del	NM_199133.4:c.16+596dup	NM_199133.4:c.16+595_16+596dup	NM_199133.4:c.16+594_16+596dup	NM_199133.4:c.16+593_16+596dup	NM_199133.4:c.16+592_16+596dup	NM_199133.4:c.16+589_16+596dup
FAM173B transcript variant X1	XM_005248248.1:c.-234+690=	XM_005248248.1:c.-234+679_-234+690del	XM_005248248.1:c.-234+680_-234+690del	XM_005248248.1:c.-234+682_-234+690del	XM_005248248.1:c.-234+684_-234+690del	XM_005248248.1:c.-234+685_-234+690del	XM_005248248.1:c.-234+686_-234+690del	XM_005248248.1:c.-234+687_-234+690del	XM_005248248.1:c.-234+688_-234+690del	XM_005248248.1:c.-234+689_-234+690del	XM_005248248.1:c.-234+690del	XM_005248248.1:c.-234+690dup	XM_005248248.1:c.-234+689_-234+690dup	XM_005248248.1:c.-234+688_-234+690dup	XM_005248248.1:c.-234+687_-234+690dup	XM_005248248.1:c.-234+686_-234+690dup	XM_005248248.1:c.-234+683_-234+690dup
ATPSCKMT transcript variant X2	XM_011513964.2:c.16+596=	XM_011513964.2:c.16+585_16+596del	XM_011513964.2:c.16+586_16+596del	XM_011513964.2:c.16+588_16+596del	XM_011513964.2:c.16+590_16+596del	XM_011513964.2:c.16+591_16+596del	XM_011513964.2:c.16+592_16+596del	XM_011513964.2:c.16+593_16+596del	XM_011513964.2:c.16+594_16+596del	XM_011513964.2:c.16+595_16+596del	XM_011513964.2:c.16+596del	XM_011513964.2:c.16+596dup	XM_011513964.2:c.16+595_16+596dup	XM_011513964.2:c.16+594_16+596dup	XM_011513964.2:c.16+593_16+596dup	XM_011513964.2:c.16+592_16+596dup	XM_011513964.2:c.16+589_16+596dup
ATPSCKMT transcript variant X1	XM_047416713.1:c.16+596=	XM_047416713.1:c.16+585_16+596del	XM_047416713.1:c.16+586_16+596del	XM_047416713.1:c.16+588_16+596del	XM_047416713.1:c.16+590_16+596del	XM_047416713.1:c.16+591_16+596del	XM_047416713.1:c.16+592_16+596del	XM_047416713.1:c.16+593_16+596del	XM_047416713.1:c.16+594_16+596del	XM_047416713.1:c.16+595_16+596del	XM_047416713.1:c.16+596del	XM_047416713.1:c.16+596dup	XM_047416713.1:c.16+595_16+596dup	XM_047416713.1:c.16+594_16+596dup	XM_047416713.1:c.16+593_16+596dup	XM_047416713.1:c.16+592_16+596dup	XM_047416713.1:c.16+589_16+596dup

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

52 SubSNP, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42553563	Dec 03, 2013 (138)
2	HUMANGENOME_JCVI	ss95385911	Dec 05, 2013 (138)
3	PJP	ss295212258	May 09, 2011 (134)
4	EVA_UK10K_ALSPAC	ss1704559253	Apr 01, 2015 (144)
5	EVA_UK10K_TWINSUK	ss1704559712	Apr 01, 2015 (144)
6	EVA_UK10K_ALSPAC	ss1710194596	Apr 01, 2015 (144)
7	EVA_UK10K_ALSPAC	ss1710194598	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1710194602	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1710194604	Apr 01, 2015 (144)
10	SWEGEN	ss2996432610	Nov 08, 2017 (151)
11	URBANLAB	ss3647985679	Oct 12, 2018 (152)
12	EVA_DECODE	ss3714096642	Jul 13, 2019 (153)
13	EVA_DECODE	ss3714096643	Jul 13, 2019 (153)
14	EVA_DECODE	ss3714096644	Jul 13, 2019 (153)
15	EVA_DECODE	ss3714096645	Jul 13, 2019 (153)
16	EVA_DECODE	ss3714096646	Jul 13, 2019 (153)
17	EVA_DECODE	ss3714096647	Jul 13, 2019 (153)
18	PACBIO	ss3785023543	Jul 13, 2019 (153)
19	PACBIO	ss3795318347	Jul 13, 2019 (153)
20	EVA	ss3829093877	Apr 26, 2020 (154)
21	GNOMAD	ss4099209014	Apr 26, 2021 (155)
22	GNOMAD	ss4099209015	Apr 26, 2021 (155)
23	GNOMAD	ss4099209016	Apr 26, 2021 (155)
24	GNOMAD	ss4099209017	Apr 26, 2021 (155)
25	GNOMAD	ss4099209020	Apr 26, 2021 (155)
26	GNOMAD	ss4099209021	Apr 26, 2021 (155)
27	GNOMAD	ss4099209022	Apr 26, 2021 (155)
28	GNOMAD	ss4099209023	Apr 26, 2021 (155)
29	GNOMAD	ss4099209024	Apr 26, 2021 (155)
30	GNOMAD	ss4099209025	Apr 26, 2021 (155)
31	GNOMAD	ss4099209026	Apr 26, 2021 (155)
32	GNOMAD	ss4099209027	Apr 26, 2021 (155)
33	GNOMAD	ss4099209028	Apr 26, 2021 (155)
34	GNOMAD	ss4099209029	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5170361125	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5170361126	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5170361127	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5170361128	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5170361129	Apr 26, 2021 (155)
40	1000G_HIGH_COVERAGE	ss5262863527	Oct 13, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5262863528	Oct 13, 2022 (156)
42	HUGCELL_USP	ss5461211518	Oct 13, 2022 (156)
43	HUGCELL_USP	ss5461211519	Oct 13, 2022 (156)
44	HUGCELL_USP	ss5461211520	Oct 13, 2022 (156)
45	HUGCELL_USP	ss5461211521	Oct 13, 2022 (156)
46	TOMMO_GENOMICS	ss5706028796	Oct 13, 2022 (156)
47	TOMMO_GENOMICS	ss5706028797	Oct 13, 2022 (156)
48	TOMMO_GENOMICS	ss5706028798	Oct 13, 2022 (156)
49	TOMMO_GENOMICS	ss5706028800	Oct 13, 2022 (156)
50	EVA	ss5834514355	Oct 13, 2022 (156)
51	EVA	ss5834514356	Oct 13, 2022 (156)
52	EVA	ss5834514357	Oct 13, 2022 (156)
53	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 14157761 (NC_000005.9:10249373:AAA: 717/3854) Row 14157763 (NC_000005.9:10249374:A: 1946/3854)	-	Oct 12, 2018 (152)
54	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 14157761 (NC_000005.9:10249373:AAA: 717/3854) Row 14157763 (NC_000005.9:10249374:A: 1946/3854)	-	Oct 12, 2018 (152)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179796860 (NC_000005.10:10249261::A 3700/85116) Row 179796861 (NC_000005.10:10249261::AA 3775/85170) Row 179796862 (NC_000005.10:10249261::AAA 23/85268)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179796860 (NC_000005.10:10249261::A 3700/85116) Row 179796861 (NC_000005.10:10249261::AA 3775/85170) Row 179796862 (NC_000005.10:10249261::AAA 23/85268)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179796860 (NC_000005.10:10249261::A 3700/85116) Row 179796861 (NC_000005.10:10249261::AA 3775/85170) Row 179796862 (NC_000005.10:10249261::AAA 23/85268)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179796860 (NC_000005.10:10249261::A 3700/85116) Row 179796861 (NC_000005.10:10249261::AA 3775/85170) Row 179796862 (NC_000005.10:10249261::AAA 23/85268)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179796860 (NC_000005.10:10249261::A 3700/85116) Row 179796861 (NC_000005.10:10249261::AA 3775/85170) Row 179796862 (NC_000005.10:10249261::AAA 23/85268)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179796860 (NC_000005.10:10249261::A 3700/85116) Row 179796861 (NC_000005.10:10249261::AA 3775/85170) Row 179796862 (NC_000005.10:10249261::AAA 23/85268)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179796860 (NC_000005.10:10249261::A 3700/85116) Row 179796861 (NC_000005.10:10249261::AA 3775/85170) Row 179796862 (NC_000005.10:10249261::AAA 23/85268)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179796860 (NC_000005.10:10249261::A 3700/85116) Row 179796861 (NC_000005.10:10249261::AA 3775/85170) Row 179796862 (NC_000005.10:10249261::AAA 23/85268)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179796860 (NC_000005.10:10249261::A 3700/85116) Row 179796861 (NC_000005.10:10249261::AA 3775/85170) Row 179796862 (NC_000005.10:10249261::AAA 23/85268)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179796860 (NC_000005.10:10249261::A 3700/85116) Row 179796861 (NC_000005.10:10249261::AA 3775/85170) Row 179796862 (NC_000005.10:10249261::AAA 23/85268)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179796860 (NC_000005.10:10249261::A 3700/85116) Row 179796861 (NC_000005.10:10249261::AA 3775/85170) Row 179796862 (NC_000005.10:10249261::AAA 23/85268)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179796860 (NC_000005.10:10249261::A 3700/85116) Row 179796861 (NC_000005.10:10249261::AA 3775/85170) Row 179796862 (NC_000005.10:10249261::AAA 23/85268)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179796860 (NC_000005.10:10249261::A 3700/85116) Row 179796861 (NC_000005.10:10249261::AA 3775/85170) Row 179796862 (NC_000005.10:10249261::AAA 23/85268)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179796860 (NC_000005.10:10249261::A 3700/85116) Row 179796861 (NC_000005.10:10249261::AA 3775/85170) Row 179796862 (NC_000005.10:10249261::AAA 23/85268)...	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 28330432 (NC_000005.9:10249373:A: 782/16744) Row 28330433 (NC_000005.9:10249373::A 102/16744) Row 28330434 (NC_000005.9:10249373:AAAAAAAAA: 46/16744)...	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 28330432 (NC_000005.9:10249373:A: 782/16744) Row 28330433 (NC_000005.9:10249373::A 102/16744) Row 28330434 (NC_000005.9:10249373:AAAAAAAAA: 46/16744)...	-	Apr 26, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 28330432 (NC_000005.9:10249373:A: 782/16744) Row 28330433 (NC_000005.9:10249373::A 102/16744) Row 28330434 (NC_000005.9:10249373:AAAAAAAAA: 46/16744)...	-	Apr 26, 2021 (155)
72	8.3KJPN Submission ignored due to conflicting rows: Row 28330432 (NC_000005.9:10249373:A: 782/16744) Row 28330433 (NC_000005.9:10249373::A 102/16744) Row 28330434 (NC_000005.9:10249373:AAAAAAAAA: 46/16744)...	-	Apr 26, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 28330432 (NC_000005.9:10249373:A: 782/16744) Row 28330433 (NC_000005.9:10249373::A 102/16744) Row 28330434 (NC_000005.9:10249373:AAAAAAAAA: 46/16744)...	-	Apr 26, 2021 (155)
74	14KJPN Submission ignored due to conflicting rows: Row 39865900 (NC_000005.10:10249261:A: 1483/28238) Row 39865901 (NC_000005.10:10249261::A 170/28238) Row 39865902 (NC_000005.10:10249261:AAAAAAAAA: 74/28238)...	-	Oct 13, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 39865900 (NC_000005.10:10249261:A: 1483/28238) Row 39865901 (NC_000005.10:10249261::A 170/28238) Row 39865902 (NC_000005.10:10249261:AAAAAAAAA: 74/28238)...	-	Oct 13, 2022 (156)
76	14KJPN Submission ignored due to conflicting rows: Row 39865900 (NC_000005.10:10249261:A: 1483/28238) Row 39865901 (NC_000005.10:10249261::A 170/28238) Row 39865902 (NC_000005.10:10249261:AAAAAAAAA: 74/28238)...	-	Oct 13, 2022 (156)
77	14KJPN Submission ignored due to conflicting rows: Row 39865900 (NC_000005.10:10249261:A: 1483/28238) Row 39865901 (NC_000005.10:10249261::A 170/28238) Row 39865902 (NC_000005.10:10249261:AAAAAAAAA: 74/28238)...	-	Oct 13, 2022 (156)
78	UK 10K study - Twins Submission ignored due to conflicting rows: Row 14157761 (NC_000005.9:10249373:AAA: 651/3708) Row 14157763 (NC_000005.9:10249374:A: 1908/3708)	-	Oct 12, 2018 (152)
79	UK 10K study - Twins Submission ignored due to conflicting rows: Row 14157761 (NC_000005.9:10249373:AAA: 651/3708) Row 14157762 (NC_000005.9:10249375:A: 784/3708) Row 14157763 (NC_000005.9:10249374:AA: 1908/3708)	-	Apr 26, 2020 (154)
80	UK 10K study - Twins Submission ignored due to conflicting rows: Row 14157761 (NC_000005.9:10249373:AAA: 651/3708) Row 14157763 (NC_000005.9:10249374:A: 1908/3708)	-	Oct 12, 2018 (152)
81	ALFA	NC_000005.10 - 10249262	Apr 26, 2021 (155)

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

Associated ID	History Updated (Build)
rs34312206	May 11, 2012 (137)
rs72277310	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4099209029	NC_000005.10:10249261:AAAAAAAAAAAA:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
4352590919	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss2996432610	NC_000005.9:10249373:AAAAAAAAAAA:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4099209028	NC_000005.10:10249261:AAAAAAAAAAA:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
4352590919	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss5170361127	NC_000005.9:10249373:AAAAAAAAA:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4099209027, ss5706028798	NC_000005.10:10249261:AAAAAAAAA:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
4352590919	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4099209026	NC_000005.10:10249261:AAAAAAA:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
4352590919	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4099209025	NC_000005.10:10249261:AAAAAA:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
4352590919	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4099209024	NC_000005.10:10249261:AAAAA:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
4352590919	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5170361129	NC_000005.9:10249373:AAAA:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3714096647, ss4099209023	NC_000005.10:10249261:AAAA:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
4352590919	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss1704559253, ss1704559712, ss5834514357	NC_000005.9:10249373:AAA:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4099209022	NC_000005.10:10249261:AAA:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
4352590919	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3714096646	NC_000005.10:10249262:AAA:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5170361128, ss5834514355	NC_000005.9:10249373:AA:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss1710194598, ss1710194604	NC_000005.9:10249374:AA:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4099209021, ss5461211518	NC_000005.10:10249261:AA:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
4352590919	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3714096645	NC_000005.10:10249263:AA:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss295212258	NC_000005.8:10302373:A:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3785023543, ss3795318347, ss3829093877, ss5170361125, ss5834514356	NC_000005.9:10249373:A:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
	NC_000005.9:10249374:A:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss1710194596, ss1710194602	NC_000005.9:10249375:A:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3647985679, ss4099209020, ss5262863527, ss5461211519, ss5706028796	NC_000005.10:10249261:A:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
4352590919	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3714096644	NC_000005.10:10249264:A:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss42553563, ss95385911	NT_006576.16:10239393:A:	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5170361126	NC_000005.9:10249373::A	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4099209014, ss5262863528, ss5461211520, ss5706028797	NC_000005.10:10249261::A	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
4352590919	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3714096643	NC_000005.10:10249265::A	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4099209015, ss5461211521	NC_000005.10:10249261::AA	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
4352590919	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3714096642	NC_000005.10:10249265::AA	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4099209016	NC_000005.10:10249261::AAA	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
4352590919	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4099209017	NC_000005.10:10249261::AAAA	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4352590919	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5706028800	NC_000005.10:10249261::AAAAAAAA	NC_000005.10:10249261:AAAAAAAAAAAA… NC_000005.10:10249261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA

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

No publications for rs5865886

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

rs5865886