Name: rs34278624
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.

rs34278624

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:57855946-57855960 (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 / delAAA / delAA / delA / …
del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dup(A)₇
Variation Type: Indel Insertion and Deletion
Frequency: delAA=0.0350 (135/3854, ALSPAC)
delAA=0.0000 (0/1044, ALFA)
delA=0.0000 (0/1044, ALFA) (+ 2 more)
dupA=0.0000 (0/1044, ALFA)
dupAA=0.0000 (0/1044, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: KIFC3 : 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	Alt HMOZ	HTRZ	HWEP
Total	Global	1044	AAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
European	Sub	424	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	542	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	26	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	516	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	2	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	0	AAAAAAAAAAAAAAA=0	AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	2	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	4	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	24	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	6	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	42	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	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
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(A)₁₅=0.9650	delAA=0.0350
Allele Frequency Aggregator	Total	Global	1044	(A)₁₅=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	542	(A)₁₅=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	European	Sub	424	(A)₁₅=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	42	(A)₁₅=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 2	Sub	24	(A)₁₅=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	6	(A)₁₅=1.0	delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
Allele Frequency Aggregator	Latin American 1	Sub	4	(A)₁₅=1.0	delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
Allele Frequency Aggregator	Asian	Sub	2	(A)₁₅=1.0	delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0

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 16	NC_000016.10:g.57855957_57855960del
GRCh38.p14 chr 16	NC_000016.10:g.57855958_57855960del
GRCh38.p14 chr 16	NC_000016.10:g.57855959_57855960del
GRCh38.p14 chr 16	NC_000016.10:g.57855960del
GRCh38.p14 chr 16	NC_000016.10:g.57855960dup
GRCh38.p14 chr 16	NC_000016.10:g.57855959_57855960dup
GRCh38.p14 chr 16	NC_000016.10:g.57855954_57855960dup
GRCh37.p13 chr 16	NC_000016.9:g.57889861_57889864del
GRCh37.p13 chr 16	NC_000016.9:g.57889862_57889864del
GRCh37.p13 chr 16	NC_000016.9:g.57889863_57889864del
GRCh37.p13 chr 16	NC_000016.9:g.57889864del
GRCh37.p13 chr 16	NC_000016.9:g.57889864dup
GRCh37.p13 chr 16	NC_000016.9:g.57889863_57889864dup
GRCh37.p13 chr 16	NC_000016.9:g.57889858_57889864dup

Gene: KIFC3, kinesin family member C3 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
KIFC3 transcript variant 3	NM_001130099.1:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant 2	NM_001130100.2:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant 4	NM_001318710.2:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant 5	NM_001318711.2:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant 6	NM_001318712.2:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant 7	NM_001318713.2:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant 8	NM_001318714.2:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant 9	NM_001318715.2:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant 1	NM_005550.4:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant 10	NR_134678.2:n.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X2	XM_005255937.2:c.108+6780… XM_005255937.2:c.108+6780_108+6783del	N/A	Intron Variant
KIFC3 transcript variant X1	XM_006721188.2:c.108+6780… XM_006721188.2:c.108+6780_108+6783del	N/A	Intron Variant
KIFC3 transcript variant X9	XM_011523075.2:c.108+6780… XM_011523075.2:c.108+6780_108+6783del	N/A	Intron Variant
KIFC3 transcript variant X10	XM_011523076.2:c.108+6780… XM_011523076.2:c.108+6780_108+6783del	N/A	Intron Variant
KIFC3 transcript variant X3	XM_017023221.2:c.108+6780… XM_017023221.2:c.108+6780_108+6783del	N/A	Intron Variant
KIFC3 transcript variant X15	XM_047434085.1:c.108+6780… XM_047434085.1:c.108+6780_108+6783del	N/A	Intron Variant
KIFC3 transcript variant X11	XM_011523077.2:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X19	XM_011523078.2:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X25	XM_011523079.2:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X13	XM_017023224.2:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X17	XM_017023225.2:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X27	XM_024450266.2:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X29	XM_024450267.2:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X28	XM_024450268.2:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X4	XM_047434078.1:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X5	XM_047434079.1:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X6	XM_047434080.1:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X7	XM_047434081.1:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X8	XM_047434082.1:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X12	XM_047434083.1:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X14	XM_047434084.1:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X16	XM_047434086.1:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X18	XM_047434087.1:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X20	XM_047434088.1:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X21	XM_047434089.1:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X22	XM_047434090.1:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X23	XM_047434091.1:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X24	XM_047434092.1:c.	N/A	Genic Upstream Transcript Variant
KIFC3 transcript variant X26	XM_047434093.1:c.	N/A	Genic Upstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(A)₁₅=	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dup(A)₇
GRCh38.p14 chr 16	NC_000016.10:g.57855946_57855960=	NC_000016.10:g.57855957_57855960del	NC_000016.10:g.57855958_57855960del	NC_000016.10:g.57855959_57855960del	NC_000016.10:g.57855960del	NC_000016.10:g.57855960dup	NC_000016.10:g.57855959_57855960dup	NC_000016.10:g.57855954_57855960dup
GRCh37.p13 chr 16	NC_000016.9:g.57889850_57889864=	NC_000016.9:g.57889861_57889864del	NC_000016.9:g.57889862_57889864del	NC_000016.9:g.57889863_57889864del	NC_000016.9:g.57889864del	NC_000016.9:g.57889864dup	NC_000016.9:g.57889863_57889864dup	NC_000016.9:g.57889858_57889864dup
KIFC3 transcript variant X4	XM_005255937.1:c.108+6783=	XM_005255937.1:c.108+6780_108+6783del	XM_005255937.1:c.108+6781_108+6783del	XM_005255937.1:c.108+6782_108+6783del	XM_005255937.1:c.108+6783del	XM_005255937.1:c.108+6783dup	XM_005255937.1:c.108+6782_108+6783dup	XM_005255937.1:c.108+6777_108+6783dup
KIFC3 transcript variant X2	XM_005255937.2:c.108+6783=	XM_005255937.2:c.108+6780_108+6783del	XM_005255937.2:c.108+6781_108+6783del	XM_005255937.2:c.108+6782_108+6783del	XM_005255937.2:c.108+6783del	XM_005255937.2:c.108+6783dup	XM_005255937.2:c.108+6782_108+6783dup	XM_005255937.2:c.108+6777_108+6783dup
KIFC3 transcript variant X2	XM_005255938.1:c.108+6783=	XM_005255938.1:c.108+6780_108+6783del	XM_005255938.1:c.108+6781_108+6783del	XM_005255938.1:c.108+6782_108+6783del	XM_005255938.1:c.108+6783del	XM_005255938.1:c.108+6783dup	XM_005255938.1:c.108+6782_108+6783dup	XM_005255938.1:c.108+6777_108+6783dup
KIFC3 transcript variant X1	XM_006721188.2:c.108+6783=	XM_006721188.2:c.108+6780_108+6783del	XM_006721188.2:c.108+6781_108+6783del	XM_006721188.2:c.108+6782_108+6783del	XM_006721188.2:c.108+6783del	XM_006721188.2:c.108+6783dup	XM_006721188.2:c.108+6782_108+6783dup	XM_006721188.2:c.108+6777_108+6783dup
KIFC3 transcript variant X9	XM_011523075.2:c.108+6783=	XM_011523075.2:c.108+6780_108+6783del	XM_011523075.2:c.108+6781_108+6783del	XM_011523075.2:c.108+6782_108+6783del	XM_011523075.2:c.108+6783del	XM_011523075.2:c.108+6783dup	XM_011523075.2:c.108+6782_108+6783dup	XM_011523075.2:c.108+6777_108+6783dup
KIFC3 transcript variant X10	XM_011523076.2:c.108+6783=	XM_011523076.2:c.108+6780_108+6783del	XM_011523076.2:c.108+6781_108+6783del	XM_011523076.2:c.108+6782_108+6783del	XM_011523076.2:c.108+6783del	XM_011523076.2:c.108+6783dup	XM_011523076.2:c.108+6782_108+6783dup	XM_011523076.2:c.108+6777_108+6783dup
KIFC3 transcript variant X3	XM_017023221.2:c.108+6783=	XM_017023221.2:c.108+6780_108+6783del	XM_017023221.2:c.108+6781_108+6783del	XM_017023221.2:c.108+6782_108+6783del	XM_017023221.2:c.108+6783del	XM_017023221.2:c.108+6783dup	XM_017023221.2:c.108+6782_108+6783dup	XM_017023221.2:c.108+6777_108+6783dup
KIFC3 transcript variant X15	XM_047434085.1:c.108+6783=	XM_047434085.1:c.108+6780_108+6783del	XM_047434085.1:c.108+6781_108+6783del	XM_047434085.1:c.108+6782_108+6783del	XM_047434085.1:c.108+6783del	XM_047434085.1:c.108+6783dup	XM_047434085.1:c.108+6782_108+6783dup	XM_047434085.1:c.108+6777_108+6783dup

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#.

43 SubSNP, 13 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40646485	Mar 13, 2006 (126)
2	HUMANGENOME_JCVI	ss95678559	Feb 13, 2009 (137)
3	BUSHMAN	ss193420547	Jul 04, 2010 (132)
4	GMI	ss289296727	May 04, 2012 (137)
5	PJP	ss294890672	May 09, 2011 (134)
6	SSMP	ss664320082	Apr 01, 2015 (144)
7	EVA_UK10K_ALSPAC	ss1708558101	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1708558678	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1710703123	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1710703140	Apr 01, 2015 (144)
11	SWEGEN	ss3014582347	Nov 08, 2017 (151)
12	MCHAISSO	ss3063846902	Nov 08, 2017 (151)
13	BEROUKHIMLAB	ss3644401502	Oct 12, 2018 (152)
14	BIOINF_KMB_FNS_UNIBA	ss3645421222	Oct 12, 2018 (152)
15	URBANLAB	ss3650519393	Oct 12, 2018 (152)
16	EVA_DECODE	ss3699347636	Jul 13, 2019 (153)
17	EVA_DECODE	ss3699347637	Jul 13, 2019 (153)
18	EVA_DECODE	ss3699347638	Jul 13, 2019 (153)
19	EVA_DECODE	ss3699347639	Jul 13, 2019 (153)
20	EVA_DECODE	ss3699347640	Jul 13, 2019 (153)
21	PACBIO	ss3788051830	Jul 13, 2019 (153)
22	PACBIO	ss3793032823	Jul 13, 2019 (153)
23	PACBIO	ss3797917820	Jul 13, 2019 (153)
24	EVA	ss3834591850	Apr 27, 2020 (154)
25	EVA	ss3840901521	Apr 27, 2020 (154)
26	EVA	ss3846393499	Apr 27, 2020 (154)
27	GNOMAD	ss4301725838	Apr 26, 2021 (155)
28	GNOMAD	ss4301725839	Apr 26, 2021 (155)
29	GNOMAD	ss4301725840	Apr 26, 2021 (155)
30	GNOMAD	ss4301725841	Apr 26, 2021 (155)
31	GNOMAD	ss4301725842	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5219764621	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5219764622	Apr 26, 2021 (155)
34	1000G_HIGH_COVERAGE	ss5301107573	Oct 16, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5301107575	Oct 16, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5301107576	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5494445596	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5494445597	Oct 16, 2022 (156)
39	HUGCELL_USP	ss5494445598	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5774830356	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5774830357	Oct 16, 2022 (156)
42	EVA	ss5851584910	Oct 16, 2022 (156)
43	EVA	ss5980923933	Oct 16, 2022 (156)
44	The Avon Longitudinal Study of Parents and Children	NC_000016.9 - 57889850	Oct 12, 2018 (152)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 490785650 (NC_000016.10:57855945::A 517/113066) Row 490785651 (NC_000016.10:57855945::AA 3/113108) Row 490785653 (NC_000016.10:57855945:A: 78064/112914)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 490785650 (NC_000016.10:57855945::A 517/113066) Row 490785651 (NC_000016.10:57855945::AA 3/113108) Row 490785653 (NC_000016.10:57855945:A: 78064/112914)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 490785650 (NC_000016.10:57855945::A 517/113066) Row 490785651 (NC_000016.10:57855945::AA 3/113108) Row 490785653 (NC_000016.10:57855945:A: 78064/112914)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 490785650 (NC_000016.10:57855945::A 517/113066) Row 490785651 (NC_000016.10:57855945::AA 3/113108) Row 490785653 (NC_000016.10:57855945:A: 78064/112914)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 490785650 (NC_000016.10:57855945::A 517/113066) Row 490785651 (NC_000016.10:57855945::AA 3/113108) Row 490785653 (NC_000016.10:57855945:A: 78064/112914)...	-	Apr 26, 2021 (155)
50	8.3KJPN Submission ignored due to conflicting rows: Row 77733928 (NC_000016.9:57889849:A: 15497/16718) Row 77733929 (NC_000016.9:57889849:AA: 123/16718)	-	Apr 26, 2021 (155)
51	8.3KJPN Submission ignored due to conflicting rows: Row 77733928 (NC_000016.9:57889849:A: 15497/16718) Row 77733929 (NC_000016.9:57889849:AA: 123/16718)	-	Apr 26, 2021 (155)
52	14KJPN Submission ignored due to conflicting rows: Row 108667460 (NC_000016.10:57855945:A: 21075/23716) Row 108667461 (NC_000016.10:57855945:AA: 171/23716)	-	Oct 16, 2022 (156)
53	14KJPN Submission ignored due to conflicting rows: Row 108667460 (NC_000016.10:57855945:A: 21075/23716) Row 108667461 (NC_000016.10:57855945:AA: 171/23716)	-	Oct 16, 2022 (156)
54	UK 10K study - Twins Submission ignored due to conflicting rows: Row 38599087 (NC_000016.9:57889850:A: 2893/3708) Row 38599088 (NC_000016.9:57889849:AA: 114/3708)	-	Apr 27, 2020 (154)
55	UK 10K study - Twins	-	Oct 12, 2018 (152)
56	ALFA	NC_000016.10 - 57855946	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)
rs71155206	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5980923933	NC_000016.9:57889849:AAAA:	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAA
ss3699347640, ss4301725842	NC_000016.10:57855945:AAA:	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
38599088, ss1708558101, ss1708558678, ss3014582347, ss5219764622	NC_000016.9:57889849:AA:	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4301725841, ss5301107575, ss5494445597, ss5774830357	NC_000016.10:57855945:AA:	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
1133710257	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3699347639	NC_000016.10:57855946:AA:	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss289296727, ss294890672	NC_000016.8:56447350:A:	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss664320082, ss3644401502, ss3788051830, ss3793032823, ss3797917820, ss3834591850, ss3840901521, ss5219764621	NC_000016.9:57889849:A:	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss1710703123, ss1710703140	NC_000016.9:57889850:A:	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3063846902, ss3645421222, ss3650519393, ss3846393499, ss4301725840, ss5301107573, ss5494445596, ss5774830356, ss5851584910	NC_000016.10:57855945:A:	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
1133710257	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3699347638	NC_000016.10:57855947:A:	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss40646485	NT_010498.15:11504048:A:	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss95678559	NT_010498.15:11504062:A:	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss193420547	NT_010498.16:11475263:A:	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4301725838, ss5301107576, ss5494445598	NC_000016.10:57855945::A	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
1133710257	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3699347637	NC_000016.10:57855948::A	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4301725839	NC_000016.10:57855945::AA	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
1133710257	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3699347636	NC_000016.10:57855948::AAAAAAA	NC_000016.10:57855945:AAAAAAAAAAAA… NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(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 rs34278624

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
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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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs34278624