Name: rs569434507
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.

rs569434507

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:68486232-68486247 (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)₄ / delAA / delA / dupA / du…
del(A)₄ / delAA / delA / dupA / dupAA / dupAAA / dup(A)₅ / dup(A)₆ / dup(A)₈
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₄=0.00000 (0/10346, ALFA)
delAA=0.00000 (0/10346, ALFA)
delA=0.00000 (0/10346, ALFA) (+ 2 more)
dupA=0.00000 (0/10346, ALFA)
dupAA=0.00000 (0/10346, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SLC25A16 : 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	10346	AAAAAAAAAAAAAAAA=1.00000	AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAA=0.00000	1.0	N/A
European	Sub	6576	AAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	2614	AAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	108	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African American	Sub	2506	AAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	64	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	48	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	16	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	128	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Latin American 2	Sub	482	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	78	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	404	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=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	10346	(A)₁₆=1.00000	del(A)₄=0.00000, delAA=0.00000, delA=0.00000, dupA=0.00000, dupAA=0.00000
Allele Frequency Aggregator	European	Sub	6576	(A)₁₆=1.0000	del(A)₄=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	2614	(A)₁₆=1.0000	del(A)₄=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	482	(A)₁₆=1.000	del(A)₄=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	404	(A)₁₆=1.000	del(A)₄=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	128	(A)₁₆=1.000	del(A)₄=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	South Asian	Sub	78	(A)₁₆=1.00	del(A)₄=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	64	(A)₁₆=1.00	del(A)₄=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=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 10	NC_000010.11:g.68486244_68486247del
GRCh38.p14 chr 10	NC_000010.11:g.68486246_68486247del
GRCh38.p14 chr 10	NC_000010.11:g.68486247del
GRCh38.p14 chr 10	NC_000010.11:g.68486247dup
GRCh38.p14 chr 10	NC_000010.11:g.68486246_68486247dup
GRCh38.p14 chr 10	NC_000010.11:g.68486245_68486247dup
GRCh38.p14 chr 10	NC_000010.11:g.68486243_68486247dup
GRCh38.p14 chr 10	NC_000010.11:g.68486242_68486247dup
GRCh38.p14 chr 10	NC_000010.11:g.68486240_68486247dup
GRCh37.p13 chr 10	NC_000010.10:g.70246001_70246004del
GRCh37.p13 chr 10	NC_000010.10:g.70246003_70246004del
GRCh37.p13 chr 10	NC_000010.10:g.70246004del
GRCh37.p13 chr 10	NC_000010.10:g.70246004dup
GRCh37.p13 chr 10	NC_000010.10:g.70246003_70246004dup
GRCh37.p13 chr 10	NC_000010.10:g.70246002_70246004dup
GRCh37.p13 chr 10	NC_000010.10:g.70246000_70246004dup
GRCh37.p13 chr 10	NC_000010.10:g.70245999_70246004dup
GRCh37.p13 chr 10	NC_000010.10:g.70245997_70246004dup
SLC25A16 RefSeqGene	NG_046972.1:g.46289_46292del
SLC25A16 RefSeqGene	NG_046972.1:g.46291_46292del
SLC25A16 RefSeqGene	NG_046972.1:g.46292del
SLC25A16 RefSeqGene	NG_046972.1:g.46292dup
SLC25A16 RefSeqGene	NG_046972.1:g.46291_46292dup
SLC25A16 RefSeqGene	NG_046972.1:g.46290_46292dup
SLC25A16 RefSeqGene	NG_046972.1:g.46288_46292dup
SLC25A16 RefSeqGene	NG_046972.1:g.46287_46292dup
SLC25A16 RefSeqGene	NG_046972.1:g.46285_46292dup

Gene: SLC25A16, solute carrier family 25 member 16 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SLC25A16 transcript variant 2	NM_001324312.2:c.842+909_… NM_001324312.2:c.842+909_842+912del	N/A	Intron Variant
SLC25A16 transcript variant 4	NM_001324314.2:c.548+909_… NM_001324314.2:c.548+909_548+912del	N/A	Intron Variant
SLC25A16 transcript variant 5	NM_001324315.1:c.548+909_… NM_001324315.1:c.548+909_548+912del	N/A	Intron Variant
SLC25A16 transcript variant 6	NM_001324317.2:c.440+909_… NM_001324317.2:c.440+909_440+912del	N/A	Intron Variant
SLC25A16 transcript variant 1	NM_152707.4:c.842+909_842… NM_152707.4:c.842+909_842+912del	N/A	Intron Variant
SLC25A16 transcript variant 3	NM_001324313.2:c.	N/A	Genic Downstream Transcript Variant
SLC25A16 transcript variant 7	NR_136737.1:n.	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)₁₆=	del(A)₄	delAA	delA	dupA	dupAA	dupAAA	dup(A)₅	dup(A)₆	dup(A)₈
GRCh38.p14 chr 10	NC_000010.11:g.68486232_68486247=	NC_000010.11:g.68486244_68486247del	NC_000010.11:g.68486246_68486247del	NC_000010.11:g.68486247del	NC_000010.11:g.68486247dup	NC_000010.11:g.68486246_68486247dup	NC_000010.11:g.68486245_68486247dup	NC_000010.11:g.68486243_68486247dup	NC_000010.11:g.68486242_68486247dup	NC_000010.11:g.68486240_68486247dup
GRCh37.p13 chr 10	NC_000010.10:g.70245989_70246004=	NC_000010.10:g.70246001_70246004del	NC_000010.10:g.70246003_70246004del	NC_000010.10:g.70246004del	NC_000010.10:g.70246004dup	NC_000010.10:g.70246003_70246004dup	NC_000010.10:g.70246002_70246004dup	NC_000010.10:g.70246000_70246004dup	NC_000010.10:g.70245999_70246004dup	NC_000010.10:g.70245997_70246004dup
SLC25A16 RefSeqGene	NG_046972.1:g.46277_46292=	NG_046972.1:g.46289_46292del	NG_046972.1:g.46291_46292del	NG_046972.1:g.46292del	NG_046972.1:g.46292dup	NG_046972.1:g.46291_46292dup	NG_046972.1:g.46290_46292dup	NG_046972.1:g.46288_46292dup	NG_046972.1:g.46287_46292dup	NG_046972.1:g.46285_46292dup
SLC25A16 transcript variant 2	NM_001324312.2:c.842+912=	NM_001324312.2:c.842+909_842+912del	NM_001324312.2:c.842+911_842+912del	NM_001324312.2:c.842+912del	NM_001324312.2:c.842+912dup	NM_001324312.2:c.842+911_842+912dup	NM_001324312.2:c.842+910_842+912dup	NM_001324312.2:c.842+908_842+912dup	NM_001324312.2:c.842+907_842+912dup	NM_001324312.2:c.842+905_842+912dup
SLC25A16 transcript variant 4	NM_001324314.2:c.548+912=	NM_001324314.2:c.548+909_548+912del	NM_001324314.2:c.548+911_548+912del	NM_001324314.2:c.548+912del	NM_001324314.2:c.548+912dup	NM_001324314.2:c.548+911_548+912dup	NM_001324314.2:c.548+910_548+912dup	NM_001324314.2:c.548+908_548+912dup	NM_001324314.2:c.548+907_548+912dup	NM_001324314.2:c.548+905_548+912dup
SLC25A16 transcript variant 5	NM_001324315.1:c.548+912=	NM_001324315.1:c.548+909_548+912del	NM_001324315.1:c.548+911_548+912del	NM_001324315.1:c.548+912del	NM_001324315.1:c.548+912dup	NM_001324315.1:c.548+911_548+912dup	NM_001324315.1:c.548+910_548+912dup	NM_001324315.1:c.548+908_548+912dup	NM_001324315.1:c.548+907_548+912dup	NM_001324315.1:c.548+905_548+912dup
SLC25A16 transcript variant 6	NM_001324317.2:c.440+912=	NM_001324317.2:c.440+909_440+912del	NM_001324317.2:c.440+911_440+912del	NM_001324317.2:c.440+912del	NM_001324317.2:c.440+912dup	NM_001324317.2:c.440+911_440+912dup	NM_001324317.2:c.440+910_440+912dup	NM_001324317.2:c.440+908_440+912dup	NM_001324317.2:c.440+907_440+912dup	NM_001324317.2:c.440+905_440+912dup
SLC25A16 transcript variant 1	NM_152707.3:c.842+912=	NM_152707.3:c.842+909_842+912del	NM_152707.3:c.842+911_842+912del	NM_152707.3:c.842+912del	NM_152707.3:c.842+912dup	NM_152707.3:c.842+911_842+912dup	NM_152707.3:c.842+910_842+912dup	NM_152707.3:c.842+908_842+912dup	NM_152707.3:c.842+907_842+912dup	NM_152707.3:c.842+905_842+912dup
SLC25A16 transcript variant 1	NM_152707.4:c.842+912=	NM_152707.4:c.842+909_842+912del	NM_152707.4:c.842+911_842+912del	NM_152707.4:c.842+912del	NM_152707.4:c.842+912dup	NM_152707.4:c.842+911_842+912dup	NM_152707.4:c.842+910_842+912dup	NM_152707.4:c.842+908_842+912dup	NM_152707.4:c.842+907_842+912dup	NM_152707.4:c.842+905_842+912dup
SLC25A16 transcript variant X1	XM_005270181.1:c.842+912=	XM_005270181.1:c.842+909_842+912del	XM_005270181.1:c.842+911_842+912del	XM_005270181.1:c.842+912del	XM_005270181.1:c.842+912dup	XM_005270181.1:c.842+911_842+912dup	XM_005270181.1:c.842+910_842+912dup	XM_005270181.1:c.842+908_842+912dup	XM_005270181.1:c.842+907_842+912dup	XM_005270181.1:c.842+905_842+912dup
SLC25A16 transcript variant X2	XM_005270182.1:c.548+912=	XM_005270182.1:c.548+909_548+912del	XM_005270182.1:c.548+911_548+912del	XM_005270182.1:c.548+912del	XM_005270182.1:c.548+912dup	XM_005270182.1:c.548+911_548+912dup	XM_005270182.1:c.548+910_548+912dup	XM_005270182.1:c.548+908_548+912dup	XM_005270182.1:c.548+907_548+912dup	XM_005270182.1:c.548+905_548+912dup
SLC25A16 transcript variant X3	XM_005270183.1:c.419+912=	XM_005270183.1:c.419+909_419+912del	XM_005270183.1:c.419+911_419+912del	XM_005270183.1:c.419+912del	XM_005270183.1:c.419+912dup	XM_005270183.1:c.419+911_419+912dup	XM_005270183.1:c.419+910_419+912dup	XM_005270183.1:c.419+908_419+912dup	XM_005270183.1:c.419+907_419+912dup	XM_005270183.1:c.419+905_419+912dup

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#.

25 SubSNP, 17 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SSIP	ss947260606	Aug 21, 2014 (142)
2	MCHAISSO	ss3063658301	Nov 08, 2017 (151)
3	ACPOP	ss3737423364	Jul 13, 2019 (153)
4	ACPOP	ss3737423366	Jul 13, 2019 (153)
5	PACBIO	ss3786705572	Jul 13, 2019 (153)
6	EVA	ss3839631765	Apr 26, 2020 (154)
7	EVA	ss3845104412	Apr 26, 2020 (154)
8	GNOMAD	ss4220473686	Apr 26, 2021 (155)
9	GNOMAD	ss4220473687	Apr 26, 2021 (155)
10	GNOMAD	ss4220473688	Apr 26, 2021 (155)
11	GNOMAD	ss4220473689	Apr 26, 2021 (155)
12	GNOMAD	ss4220473690	Apr 26, 2021 (155)
13	GNOMAD	ss4220473691	Apr 26, 2021 (155)
14	GNOMAD	ss4220473693	Apr 26, 2021 (155)
15	GNOMAD	ss4220473694	Apr 26, 2021 (155)
16	TOMMO_GENOMICS	ss5198134593	Apr 26, 2021 (155)
17	TOMMO_GENOMICS	ss5198134594	Apr 26, 2021 (155)
18	TOMMO_GENOMICS	ss5198134595	Apr 26, 2021 (155)
19	1000G_HIGH_COVERAGE	ss5284442809	Oct 16, 2022 (156)
20	1000G_HIGH_COVERAGE	ss5284442811	Oct 16, 2022 (156)
21	HUGCELL_USP	ss5479980985	Oct 16, 2022 (156)
22	HUGCELL_USP	ss5479980986	Oct 16, 2022 (156)
23	TOMMO_GENOMICS	ss5744108398	Oct 16, 2022 (156)
24	TOMMO_GENOMICS	ss5744108399	Oct 16, 2022 (156)
25	TOMMO_GENOMICS	ss5744108400	Oct 16, 2022 (156)
26	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355449296 (NC_000010.11:68486231::A 4105/77794) Row 355449297 (NC_000010.11:68486231::AA 18/77854) Row 355449298 (NC_000010.11:68486231::AAA 1/77860)...	-	Apr 26, 2021 (155)
27	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355449296 (NC_000010.11:68486231::A 4105/77794) Row 355449297 (NC_000010.11:68486231::AA 18/77854) Row 355449298 (NC_000010.11:68486231::AAA 1/77860)...	-	Apr 26, 2021 (155)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355449296 (NC_000010.11:68486231::A 4105/77794) Row 355449297 (NC_000010.11:68486231::AA 18/77854) Row 355449298 (NC_000010.11:68486231::AAA 1/77860)...	-	Apr 26, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355449296 (NC_000010.11:68486231::A 4105/77794) Row 355449297 (NC_000010.11:68486231::AA 18/77854) Row 355449298 (NC_000010.11:68486231::AAA 1/77860)...	-	Apr 26, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355449296 (NC_000010.11:68486231::A 4105/77794) Row 355449297 (NC_000010.11:68486231::AA 18/77854) Row 355449298 (NC_000010.11:68486231::AAA 1/77860)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355449296 (NC_000010.11:68486231::A 4105/77794) Row 355449297 (NC_000010.11:68486231::AA 18/77854) Row 355449298 (NC_000010.11:68486231::AAA 1/77860)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355449296 (NC_000010.11:68486231::A 4105/77794) Row 355449297 (NC_000010.11:68486231::AA 18/77854) Row 355449298 (NC_000010.11:68486231::AAA 1/77860)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355449296 (NC_000010.11:68486231::A 4105/77794) Row 355449297 (NC_000010.11:68486231::AA 18/77854) Row 355449298 (NC_000010.11:68486231::AAA 1/77860)...	-	Apr 26, 2021 (155)
34	Northern Sweden Submission ignored due to conflicting rows: Row 10708229 (NC_000010.10:70245988::A 11/556) Row 10708231 (NC_000010.10:70245988:A: 13/556)	-	Jul 13, 2019 (153)
35	Northern Sweden Submission ignored due to conflicting rows: Row 10708229 (NC_000010.10:70245988::A 11/556) Row 10708231 (NC_000010.10:70245988:A: 13/556)	-	Jul 13, 2019 (153)
36	8.3KJPN Submission ignored due to conflicting rows: Row 56103900 (NC_000010.10:70245988::AA 9/16628) Row 56103901 (NC_000010.10:70245988::A 2160/16628) Row 56103902 (NC_000010.10:70245988:A: 165/16628)	-	Apr 26, 2021 (155)
37	8.3KJPN Submission ignored due to conflicting rows: Row 56103900 (NC_000010.10:70245988::AA 9/16628) Row 56103901 (NC_000010.10:70245988::A 2160/16628) Row 56103902 (NC_000010.10:70245988:A: 165/16628)	-	Apr 26, 2021 (155)
38	8.3KJPN Submission ignored due to conflicting rows: Row 56103900 (NC_000010.10:70245988::AA 9/16628) Row 56103901 (NC_000010.10:70245988::A 2160/16628) Row 56103902 (NC_000010.10:70245988:A: 165/16628)	-	Apr 26, 2021 (155)
39	14KJPN Submission ignored due to conflicting rows: Row 77945502 (NC_000010.11:68486231::A 3874/28230) Row 77945503 (NC_000010.11:68486231:A: 300/28230) Row 77945504 (NC_000010.11:68486231::AA 17/28230)	-	Oct 16, 2022 (156)
40	14KJPN Submission ignored due to conflicting rows: Row 77945502 (NC_000010.11:68486231::A 3874/28230) Row 77945503 (NC_000010.11:68486231:A: 300/28230) Row 77945504 (NC_000010.11:68486231::AA 17/28230)	-	Oct 16, 2022 (156)
41	14KJPN Submission ignored due to conflicting rows: Row 77945502 (NC_000010.11:68486231::A 3874/28230) Row 77945503 (NC_000010.11:68486231:A: 300/28230) Row 77945504 (NC_000010.11:68486231::AA 17/28230)	-	Oct 16, 2022 (156)
42	ALFA	NC_000010.11 - 68486232	Apr 26, 2021 (155)

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

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
6950989652	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4220473694	NC_000010.11:68486231:AA:	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
6950989652	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss947260606, ss3737423366, ss3786705572, ss3839631765, ss5198134595	NC_000010.10:70245988:A:	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3845104412, ss4220473693, ss5284442809, ss5479980986, ss5744108399	NC_000010.11:68486231:A:	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
6950989652	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3737423364, ss5198134594	NC_000010.10:70245988::A	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3063658301, ss4220473686, ss5284442811, ss5479980985, ss5744108398	NC_000010.11:68486231::A	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
6950989652	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5198134593	NC_000010.10:70245988::AA	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4220473687, ss5744108400	NC_000010.11:68486231::AA	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
6950989652	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4220473688	NC_000010.11:68486231::AAA	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4220473689	NC_000010.11:68486231::AAAAA	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4220473690	NC_000010.11:68486231::AAAAAA	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220473691	NC_000010.11:68486231::AAAAAAAA	NC_000010.11:68486231:AAAAAAAAAAAA… NC_000010.11:68486231:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(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 rs569434507

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

rs569434507