Name: rs35355726
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.

rs35355726

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:173361453-173361469 (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(T)₅ / del(T)₄ / delTTT / delTT…
del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT
Variation Type: Indel Insertion and Deletion
Frequency: (T)₁₇=0.4061 (1794/4418, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CDCA7 : 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	4418	TTTTTTTTTTTTTTTTT=0.4061	TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.4898, TTTTTTTTTTTTTTTTTT=0.0183, TTTTTTTTTTTTTTTT=0.0858, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	0.319375	0.34115	0.339475	32
European	Sub	4394	TTTTTTTTTTTTTTTTT=0.4040	TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.4914, TTTTTTTTTTTTTTTTTT=0.0184, TTTTTTTTTTTTTTTT=0.0863, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	0.31647	0.342327	0.341203	32
African	Sub	16	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African Others	Sub	2	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	14	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Asian	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
East Asian	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 2	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
South Asian	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other	Sub	8	TTTTTTTTTTTTTTTTT=0.4	TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.6, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0	0.25	0.5	0.25	1

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	4418	(T)₁₇=0.4061	delTTT=0.0000, delTT=0.4898, delT=0.0858, dupT=0.0183, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	European	Sub	4394	(T)₁₇=0.4040	delTTT=0.0000, delTT=0.4914, delT=0.0863, dupT=0.0184, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	African	Sub	16	(T)₁₇=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Other	Sub	8	(T)₁₇=0.4	delTTT=0.0, delTT=0.6, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(T)₁₇=0	delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0
Allele Frequency Aggregator	Latin American 2	Sub	0	(T)₁₇=0	delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0
Allele Frequency Aggregator	South Asian	Sub	0	(T)₁₇=0	delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0
Allele Frequency Aggregator	Asian	Sub	0	(T)₁₇=0	delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=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 2	NC_000002.12:g.173361465_173361469del
GRCh38.p14 chr 2	NC_000002.12:g.173361466_173361469del
GRCh38.p14 chr 2	NC_000002.12:g.173361467_173361469del
GRCh38.p14 chr 2	NC_000002.12:g.173361468_173361469del
GRCh38.p14 chr 2	NC_000002.12:g.173361469del
GRCh38.p14 chr 2	NC_000002.12:g.173361469dup
GRCh38.p14 chr 2	NC_000002.12:g.173361468_173361469dup
GRCh38.p14 chr 2	NC_000002.12:g.173361467_173361469dup
GRCh37.p13 chr 2	NC_000002.11:g.174226193_174226197del
GRCh37.p13 chr 2	NC_000002.11:g.174226194_174226197del
GRCh37.p13 chr 2	NC_000002.11:g.174226195_174226197del
GRCh37.p13 chr 2	NC_000002.11:g.174226196_174226197del
GRCh37.p13 chr 2	NC_000002.11:g.174226197del
GRCh37.p13 chr 2	NC_000002.11:g.174226197dup
GRCh37.p13 chr 2	NC_000002.11:g.174226196_174226197dup
GRCh37.p13 chr 2	NC_000002.11:g.174226195_174226197dup
CDCA7 RefSeqGene	NG_047202.1:g.12449_12453del
CDCA7 RefSeqGene	NG_047202.1:g.12450_12453del
CDCA7 RefSeqGene	NG_047202.1:g.12451_12453del
CDCA7 RefSeqGene	NG_047202.1:g.12452_12453del
CDCA7 RefSeqGene	NG_047202.1:g.12453del
CDCA7 RefSeqGene	NG_047202.1:g.12453dup
CDCA7 RefSeqGene	NG_047202.1:g.12452_12453dup
CDCA7 RefSeqGene	NG_047202.1:g.12451_12453dup

Gene: CDCA7, cell division cycle associated 7 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CDCA7 transcript variant 1	NM_031942.5:c.385-1761_38… NM_031942.5:c.385-1761_385-1757del	N/A	Intron Variant
CDCA7 transcript variant 2	NM_145810.3:c.148-1761_14… NM_145810.3:c.148-1761_148-1757del	N/A	Intron Variant
CDCA7 transcript variant X1	XM_047445957.1:c.385-1761… XM_047445957.1:c.385-1761_385-1757del	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	(T)₁₇=	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT
GRCh38.p14 chr 2	NC_000002.12:g.173361453_173361469=	NC_000002.12:g.173361465_173361469del	NC_000002.12:g.173361466_173361469del	NC_000002.12:g.173361467_173361469del	NC_000002.12:g.173361468_173361469del	NC_000002.12:g.173361469del	NC_000002.12:g.173361469dup	NC_000002.12:g.173361468_173361469dup	NC_000002.12:g.173361467_173361469dup
GRCh37.p13 chr 2	NC_000002.11:g.174226181_174226197=	NC_000002.11:g.174226193_174226197del	NC_000002.11:g.174226194_174226197del	NC_000002.11:g.174226195_174226197del	NC_000002.11:g.174226196_174226197del	NC_000002.11:g.174226197del	NC_000002.11:g.174226197dup	NC_000002.11:g.174226196_174226197dup	NC_000002.11:g.174226195_174226197dup
CDCA7 RefSeqGene	NG_047202.1:g.12437_12453=	NG_047202.1:g.12449_12453del	NG_047202.1:g.12450_12453del	NG_047202.1:g.12451_12453del	NG_047202.1:g.12452_12453del	NG_047202.1:g.12453del	NG_047202.1:g.12453dup	NG_047202.1:g.12452_12453dup	NG_047202.1:g.12451_12453dup
CDCA7 transcript variant 1	NM_031942.4:c.385-1773=	NM_031942.4:c.385-1761_385-1757del	NM_031942.4:c.385-1760_385-1757del	NM_031942.4:c.385-1759_385-1757del	NM_031942.4:c.385-1758_385-1757del	NM_031942.4:c.385-1757del	NM_031942.4:c.385-1757dup	NM_031942.4:c.385-1758_385-1757dup	NM_031942.4:c.385-1759_385-1757dup
CDCA7 transcript variant 1	NM_031942.5:c.385-1773=	NM_031942.5:c.385-1761_385-1757del	NM_031942.5:c.385-1760_385-1757del	NM_031942.5:c.385-1759_385-1757del	NM_031942.5:c.385-1758_385-1757del	NM_031942.5:c.385-1757del	NM_031942.5:c.385-1757dup	NM_031942.5:c.385-1758_385-1757dup	NM_031942.5:c.385-1759_385-1757dup
CDCA7 transcript variant 2	NM_145810.2:c.148-1773=	NM_145810.2:c.148-1761_148-1757del	NM_145810.2:c.148-1760_148-1757del	NM_145810.2:c.148-1759_148-1757del	NM_145810.2:c.148-1758_148-1757del	NM_145810.2:c.148-1757del	NM_145810.2:c.148-1757dup	NM_145810.2:c.148-1758_148-1757dup	NM_145810.2:c.148-1759_148-1757dup
CDCA7 transcript variant 2	NM_145810.3:c.148-1773=	NM_145810.3:c.148-1761_148-1757del	NM_145810.3:c.148-1760_148-1757del	NM_145810.3:c.148-1759_148-1757del	NM_145810.3:c.148-1758_148-1757del	NM_145810.3:c.148-1757del	NM_145810.3:c.148-1757dup	NM_145810.3:c.148-1758_148-1757dup	NM_145810.3:c.148-1759_148-1757dup
CDCA7 transcript variant X1	XM_005246883.1:c.253-1773=	XM_005246883.1:c.253-1761_253-1757del	XM_005246883.1:c.253-1760_253-1757del	XM_005246883.1:c.253-1759_253-1757del	XM_005246883.1:c.253-1758_253-1757del	XM_005246883.1:c.253-1757del	XM_005246883.1:c.253-1757dup	XM_005246883.1:c.253-1758_253-1757dup	XM_005246883.1:c.253-1759_253-1757dup
CDCA7 transcript variant X2	XM_005246884.1:c.22-1773=	XM_005246884.1:c.22-1761_22-1757del	XM_005246884.1:c.22-1760_22-1757del	XM_005246884.1:c.22-1759_22-1757del	XM_005246884.1:c.22-1758_22-1757del	XM_005246884.1:c.22-1757del	XM_005246884.1:c.22-1757dup	XM_005246884.1:c.22-1758_22-1757dup	XM_005246884.1:c.22-1759_22-1757dup
CDCA7 transcript variant X1	XM_047445957.1:c.385-1773=	XM_047445957.1:c.385-1761_385-1757del	XM_047445957.1:c.385-1760_385-1757del	XM_047445957.1:c.385-1759_385-1757del	XM_047445957.1:c.385-1758_385-1757del	XM_047445957.1:c.385-1757del	XM_047445957.1:c.385-1757dup	XM_047445957.1:c.385-1758_385-1757dup	XM_047445957.1:c.385-1759_385-1757dup

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, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41629420	Mar 15, 2006 (137)
2	ABI	ss41689860	Dec 03, 2013 (138)
3	ABI	ss41829505	Dec 03, 2013 (138)
4	HGSV	ss77936453	Sep 08, 2015 (146)
5	HGSV	ss81841726	Sep 08, 2015 (146)
6	HGSV	ss82072607	Sep 08, 2015 (146)
7	BCMHGSC_JDW	ss103638546	Mar 15, 2016 (147)
8	GMI	ss288255673	May 04, 2012 (137)
9	PJP	ss295014876	May 09, 2011 (137)
10	PJP	ss295014877	May 09, 2011 (135)
11	SSMP	ss663259942	Apr 01, 2015 (144)
12	BILGI_BIOE	ss666176279	Apr 25, 2013 (138)
13	EVA_UK10K_TWINSUK	ss1703288618	Apr 01, 2015 (144)
14	EVA_UK10K_ALSPAC	ss1703288667	Apr 01, 2015 (144)
15	EVA_UK10K_TWINSUK	ss1710039407	Apr 01, 2015 (144)
16	EVA_UK10K_ALSPAC	ss1710039409	Apr 01, 2015 (144)
17	HAMMER_LAB	ss1797934407	Sep 08, 2015 (146)
18	SWEGEN	ss2990887942	Nov 08, 2017 (151)
19	MCHAISSO	ss3063967501	Nov 08, 2017 (151)
20	MCHAISSO	ss3064821697	Nov 08, 2017 (151)
21	MCHAISSO	ss3065779647	Nov 08, 2017 (151)
22	URBANLAB	ss3647209850	Oct 11, 2018 (152)
23	EVA_DECODE	ss3705453383	Jul 13, 2019 (153)
24	EVA_DECODE	ss3705453384	Jul 13, 2019 (153)
25	EVA_DECODE	ss3705453385	Jul 13, 2019 (153)
26	EVA_DECODE	ss3705453386	Jul 13, 2019 (153)
27	EVA_DECODE	ss3705453387	Jul 13, 2019 (153)
28	PACBIO	ss3784071874	Jul 13, 2019 (153)
29	PACBIO	ss3789623036	Jul 13, 2019 (153)
30	PACBIO	ss3789623037	Jul 13, 2019 (153)
31	PACBIO	ss3794496062	Jul 13, 2019 (153)
32	PACBIO	ss3794496063	Jul 13, 2019 (153)
33	EVA	ss3827361389	Apr 25, 2020 (154)
34	KOGIC	ss3949528960	Apr 25, 2020 (154)
35	KOGIC	ss3949528961	Apr 25, 2020 (154)
36	KOGIC	ss3949528962	Apr 25, 2020 (154)
37	GNOMAD	ss4055854310	Apr 26, 2021 (155)
38	GNOMAD	ss4055854311	Apr 26, 2021 (155)
39	GNOMAD	ss4055854312	Apr 26, 2021 (155)
40	GNOMAD	ss4055854313	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5155181600	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5155181601	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5155181602	Apr 26, 2021 (155)
44	1000G_HIGH_COVERAGE	ss5251016182	Oct 12, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5251016183	Oct 12, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5251016184	Oct 12, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5251016185	Oct 12, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5251016186	Oct 12, 2022 (156)
49	TOMMO_GENOMICS	ss5685683908	Oct 12, 2022 (156)
50	TOMMO_GENOMICS	ss5685683909	Oct 12, 2022 (156)
51	TOMMO_GENOMICS	ss5685683910	Oct 12, 2022 (156)
52	EVA	ss5933532886	Oct 12, 2022 (156)
53	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 6370399 (NC_000002.11:174226181:T: 3450/3854) Row 6370400 (NC_000002.11:174226180:TTT: 402/3854)	-	Oct 11, 2018 (152)
54	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 6370399 (NC_000002.11:174226181:T: 3450/3854) Row 6370400 (NC_000002.11:174226180:TTT: 402/3854)	-	Oct 11, 2018 (152)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 82254514 (NC_000002.12:173361452::TT 64/98330) Row 82254515 (NC_000002.12:173361452::TTT 1/98334) Row 82254516 (NC_000002.12:173361452:TTTT: 24/98324)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 82254514 (NC_000002.12:173361452::TT 64/98330) Row 82254515 (NC_000002.12:173361452::TTT 1/98334) Row 82254516 (NC_000002.12:173361452:TTTT: 24/98324)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 82254514 (NC_000002.12:173361452::TT 64/98330) Row 82254515 (NC_000002.12:173361452::TTT 1/98334) Row 82254516 (NC_000002.12:173361452:TTTT: 24/98324)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 82254514 (NC_000002.12:173361452::TT 64/98330) Row 82254515 (NC_000002.12:173361452::TTT 1/98334) Row 82254516 (NC_000002.12:173361452:TTTT: 24/98324)...	-	Apr 26, 2021 (155)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 5906961 (NC_000002.12:173361453:TT: 1437/1830) Row 5906962 (NC_000002.12:173361452:TTT: 118/1830) Row 5906963 (NC_000002.12:173361454:T: 94/1830)	-	Apr 25, 2020 (154)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 5906961 (NC_000002.12:173361453:TT: 1437/1830) Row 5906962 (NC_000002.12:173361452:TTT: 118/1830) Row 5906963 (NC_000002.12:173361454:T: 94/1830)	-	Apr 25, 2020 (154)
61	Korean Genome Project Submission ignored due to conflicting rows: Row 5906961 (NC_000002.12:173361453:TT: 1437/1830) Row 5906962 (NC_000002.12:173361452:TTT: 118/1830) Row 5906963 (NC_000002.12:173361454:T: 94/1830)	-	Apr 25, 2020 (154)
62	8.3KJPN Submission ignored due to conflicting rows: Row 13150907 (NC_000002.11:174226180:TT: 15457/16682) Row 13150908 (NC_000002.11:174226180:T: 655/16682) Row 13150909 (NC_000002.11:174226180:TTT: 17/16682)	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 13150907 (NC_000002.11:174226180:TT: 15457/16682) Row 13150908 (NC_000002.11:174226180:T: 655/16682) Row 13150909 (NC_000002.11:174226180:TTT: 17/16682)	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 13150907 (NC_000002.11:174226180:TT: 15457/16682) Row 13150908 (NC_000002.11:174226180:T: 655/16682) Row 13150909 (NC_000002.11:174226180:TTT: 17/16682)	-	Apr 26, 2021 (155)
65	14KJPN Submission ignored due to conflicting rows: Row 19521012 (NC_000002.12:173361452:TT: 24940/27372) Row 19521013 (NC_000002.12:173361452:T: 1037/27372) Row 19521014 (NC_000002.12:173361452:TTT: 26/27372)	-	Oct 12, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 19521012 (NC_000002.12:173361452:TT: 24940/27372) Row 19521013 (NC_000002.12:173361452:T: 1037/27372) Row 19521014 (NC_000002.12:173361452:TTT: 26/27372)	-	Oct 12, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 19521012 (NC_000002.12:173361452:TT: 24940/27372) Row 19521013 (NC_000002.12:173361452:T: 1037/27372) Row 19521014 (NC_000002.12:173361452:TTT: 26/27372)	-	Oct 12, 2022 (156)
68	UK 10K study - Twins Submission ignored due to conflicting rows: Row 6370399 (NC_000002.11:174226181:T: 3324/3708) Row 6370400 (NC_000002.11:174226180:TTT: 383/3708)	-	Oct 11, 2018 (152)
69	UK 10K study - Twins Submission ignored due to conflicting rows: Row 6370399 (NC_000002.11:174226181:T: 3324/3708) Row 6370400 (NC_000002.11:174226180:TTT: 383/3708)	-	Oct 11, 2018 (152)
70	ALFA	NC_000002.12 - 173361453	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)
rs59398698	May 25, 2008 (130)
rs143254089	May 11, 2012 (137)
rs151319601	Sep 17, 2011 (135)
rs35423390	May 11, 2012 (137)
rs35910288	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4055854313	NC_000002.12:173361452:TTTTT:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3705453383, ss4055854312	NC_000002.12:173361452:TTTT:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss1703288618, ss1703288667, ss5155181602	NC_000002.11:174226180:TTT:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3949528961, ss5251016185, ss5685683910	NC_000002.12:173361452:TTT:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
9435098633	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3705453384	NC_000002.12:173361453:TTT:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss77936453, ss81841726, ss82072607	NC_000002.9:174051702:TT:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss288255673, ss295014876	NC_000002.10:173934426:TT:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss295014877	NC_000002.10:173934441:TT:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss663259942, ss1797934407, ss2990887942, ss3784071874, ss3789623036, ss3794496062, ss5155181600	NC_000002.11:174226180:TT:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss1710039407, ss1710039409	NC_000002.11:174226181:TT:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3063967501, ss3064821697, ss3065779647, ss3647209850, ss5251016182, ss5685683908, ss5933532886	NC_000002.12:173361452:TT:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
9435098633	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3949528960	NC_000002.12:173361453:TT:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3705453385	NC_000002.12:173361454:TT:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss666176279, ss3789623037, ss3794496063, ss3827361389, ss5155181601	NC_000002.11:174226180:T:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
	NC_000002.11:174226181:T:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss5251016184, ss5685683909	NC_000002.12:173361452:T:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
9435098633	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3949528962	NC_000002.12:173361454:T:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3705453386	NC_000002.12:173361455:T:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss41689860	NT_005403.17:24435612:T:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss41629420	NT_005403.17:24435613:T:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss41829505	NT_005403.17:24435614:T:	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss5251016183	NC_000002.12:173361452::T	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
9435098633	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3705453387	NC_000002.12:173361456::T	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss103638546	NT_005403.17:24435615:G:TG	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4055854310, ss5251016186	NC_000002.12:173361452::TT	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
9435098633	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4055854311	NC_000002.12:173361452::TTT	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
9435098633	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000002.12:173361452:TTTTTTTTTTT… NC_000002.12:173361452:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(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 rs35355726

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

rs35355726