Name: rs111694406
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.

rs111694406

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:110585291-110585308 (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)₇ / del(T)₆ / del(T)₅ / delT…
del(T)₇ / del(T)₆ / del(T)₅ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅
Variation Type: Indel Insertion and Deletion
Frequency: dupTTT=0.02152 (276/12826, ALFA)
delT=0.1591 (797/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SMC3 : 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	12826	TTTTTTTTTTTTTTTTTT=0.95876	TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00296, TTTTTTTTTTTTTTTTTTTT=0.01676, TTTTTTTTTTTTTTTTTTTTT=0.02152, TTTTTTTTTTTTTTTTTTTTTT=0.00000	0.961159	0.002913	0.035928	32
European	Sub	10598	TTTTTTTTTTTTTTTTTT=0.95027	TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00349, TTTTTTTTTTTTTTTTTTTT=0.02019, TTTTTTTTTTTTTTTTTTTTT=0.02604, TTTTTTTTTTTTTTTTTTTTTT=0.00000	0.952635	0.003552	0.043813	N/A
African	Sub	1310	TTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	54	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1256	TTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	68	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	52	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	16	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	90	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	376	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	76	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	308	TTTTTTTTTTTTTTTTTT=0.994	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.003, TTTTTTTTTTTTTTTTTTTT=0.003, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	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
Allele Frequency Aggregator	Total	Global	12826	(T)₁₈=0.95876	del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00296, dupTT=0.01676, dupTTT=0.02152, dup(T)₄=0.00000
Allele Frequency Aggregator	European	Sub	10598	(T)₁₈=0.95027	del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00349, dupTT=0.02019, dupTTT=0.02604, dup(T)₄=0.00000
Allele Frequency Aggregator	African	Sub	1310	(T)₁₈=1.0000	del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	376	(T)₁₈=1.000	del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Other	Sub	308	(T)₁₈=0.994	del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTT=0.000, delT=0.000, dupT=0.003, dupTT=0.003, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	90	(T)₁₈=1.00	del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	76	(T)₁₈=1.00	del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Asian	Sub	68	(T)₁₈=1.00	del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
1000Genomes	Global	Study-wide	5008	(T)₁₈=0.8409	delT=0.1591
1000Genomes	African	Sub	1322	(T)₁₈=0.8419	delT=0.1581
1000Genomes	East Asian	Sub	1008	(T)₁₈=0.8651	delT=0.1349
1000Genomes	Europe	Sub	1006	(T)₁₈=0.8151	delT=0.1849
1000Genomes	South Asian	Sub	978	(T)₁₈=0.827	delT=0.173
1000Genomes	American	Sub	694	(T)₁₈=0.860	delT=0.140

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.110585302_110585308del
GRCh38.p14 chr 10	NC_000010.11:g.110585303_110585308del
GRCh38.p14 chr 10	NC_000010.11:g.110585304_110585308del
GRCh38.p14 chr 10	NC_000010.11:g.110585306_110585308del
GRCh38.p14 chr 10	NC_000010.11:g.110585307_110585308del
GRCh38.p14 chr 10	NC_000010.11:g.110585308del
GRCh38.p14 chr 10	NC_000010.11:g.110585308dup
GRCh38.p14 chr 10	NC_000010.11:g.110585307_110585308dup
GRCh38.p14 chr 10	NC_000010.11:g.110585306_110585308dup
GRCh38.p14 chr 10	NC_000010.11:g.110585305_110585308dup
GRCh38.p14 chr 10	NC_000010.11:g.110585304_110585308dup
GRCh37.p13 chr 10	NC_000010.10:g.112345060_112345066del
GRCh37.p13 chr 10	NC_000010.10:g.112345061_112345066del
GRCh37.p13 chr 10	NC_000010.10:g.112345062_112345066del
GRCh37.p13 chr 10	NC_000010.10:g.112345064_112345066del
GRCh37.p13 chr 10	NC_000010.10:g.112345065_112345066del
GRCh37.p13 chr 10	NC_000010.10:g.112345066del
GRCh37.p13 chr 10	NC_000010.10:g.112345066dup
GRCh37.p13 chr 10	NC_000010.10:g.112345065_112345066dup
GRCh37.p13 chr 10	NC_000010.10:g.112345064_112345066dup
GRCh37.p13 chr 10	NC_000010.10:g.112345063_112345066dup
GRCh37.p13 chr 10	NC_000010.10:g.112345062_112345066dup
SMC3 RefSeqGene (LRG_774)	NG_012217.1:g.22612_22618del
SMC3 RefSeqGene (LRG_774)	NG_012217.1:g.22613_22618del
SMC3 RefSeqGene (LRG_774)	NG_012217.1:g.22614_22618del
SMC3 RefSeqGene (LRG_774)	NG_012217.1:g.22616_22618del
SMC3 RefSeqGene (LRG_774)	NG_012217.1:g.22617_22618del
SMC3 RefSeqGene (LRG_774)	NG_012217.1:g.22618del
SMC3 RefSeqGene (LRG_774)	NG_012217.1:g.22618dup
SMC3 RefSeqGene (LRG_774)	NG_012217.1:g.22617_22618dup
SMC3 RefSeqGene (LRG_774)	NG_012217.1:g.22616_22618dup
SMC3 RefSeqGene (LRG_774)	NG_012217.1:g.22615_22618dup
SMC3 RefSeqGene (LRG_774)	NG_012217.1:g.22614_22618dup

Gene: SMC3, structural maintenance of chromosomes 3 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SMC3 transcript	NM_005445.4:c.1305+906_13… NM_005445.4:c.1305+906_1305+912del	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)₁₈=	del(T)₇	del(T)₆	del(T)₅	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅
GRCh38.p14 chr 10	NC_000010.11:g.110585291_110585308=	NC_000010.11:g.110585302_110585308del	NC_000010.11:g.110585303_110585308del	NC_000010.11:g.110585304_110585308del	NC_000010.11:g.110585306_110585308del	NC_000010.11:g.110585307_110585308del	NC_000010.11:g.110585308del	NC_000010.11:g.110585308dup	NC_000010.11:g.110585307_110585308dup	NC_000010.11:g.110585306_110585308dup	NC_000010.11:g.110585305_110585308dup	NC_000010.11:g.110585304_110585308dup
GRCh37.p13 chr 10	NC_000010.10:g.112345049_112345066=	NC_000010.10:g.112345060_112345066del	NC_000010.10:g.112345061_112345066del	NC_000010.10:g.112345062_112345066del	NC_000010.10:g.112345064_112345066del	NC_000010.10:g.112345065_112345066del	NC_000010.10:g.112345066del	NC_000010.10:g.112345066dup	NC_000010.10:g.112345065_112345066dup	NC_000010.10:g.112345064_112345066dup	NC_000010.10:g.112345063_112345066dup	NC_000010.10:g.112345062_112345066dup
SMC3 RefSeqGene (LRG_774)	NG_012217.1:g.22601_22618=	NG_012217.1:g.22612_22618del	NG_012217.1:g.22613_22618del	NG_012217.1:g.22614_22618del	NG_012217.1:g.22616_22618del	NG_012217.1:g.22617_22618del	NG_012217.1:g.22618del	NG_012217.1:g.22618dup	NG_012217.1:g.22617_22618dup	NG_012217.1:g.22616_22618dup	NG_012217.1:g.22615_22618dup	NG_012217.1:g.22614_22618dup
SMC3 transcript	NM_005445.3:c.1305+895=	NM_005445.3:c.1305+906_1305+912del	NM_005445.3:c.1305+907_1305+912del	NM_005445.3:c.1305+908_1305+912del	NM_005445.3:c.1305+910_1305+912del	NM_005445.3:c.1305+911_1305+912del	NM_005445.3:c.1305+912del	NM_005445.3:c.1305+912dup	NM_005445.3:c.1305+911_1305+912dup	NM_005445.3:c.1305+910_1305+912dup	NM_005445.3:c.1305+909_1305+912dup	NM_005445.3:c.1305+908_1305+912dup
SMC3 transcript	NM_005445.4:c.1305+895=	NM_005445.4:c.1305+906_1305+912del	NM_005445.4:c.1305+907_1305+912del	NM_005445.4:c.1305+908_1305+912del	NM_005445.4:c.1305+910_1305+912del	NM_005445.4:c.1305+911_1305+912del	NM_005445.4:c.1305+912del	NM_005445.4:c.1305+912dup	NM_005445.4:c.1305+911_1305+912dup	NM_005445.4:c.1305+910_1305+912dup	NM_005445.4:c.1305+909_1305+912dup	NM_005445.4:c.1305+908_1305+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#.

40 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BUSHMAN	ss193204818	Jul 04, 2010 (132)
2	SSIP	ss947266795	Aug 21, 2014 (142)
3	1000GENOMES	ss1370100948	Aug 21, 2014 (142)
4	SWEGEN	ss3007148703	Nov 08, 2017 (151)
5	SWEGEN	ss3007148704	Nov 08, 2017 (151)
6	SWEGEN	ss3007148705	Nov 08, 2017 (151)
7	ACPOP	ss3737679739	Jul 13, 2019 (153)
8	ACPOP	ss3737679740	Jul 13, 2019 (153)
9	PACBIO	ss3786786122	Jul 13, 2019 (153)
10	KHV_HUMAN_GENOMES	ss3813963106	Jul 13, 2019 (153)
11	EVA	ss3832332500	Apr 26, 2020 (154)
12	GNOMAD	ss4225600585	Apr 26, 2021 (155)
13	GNOMAD	ss4225600586	Apr 26, 2021 (155)
14	GNOMAD	ss4225600587	Apr 26, 2021 (155)
15	GNOMAD	ss4225600588	Apr 26, 2021 (155)
16	GNOMAD	ss4225600589	Apr 26, 2021 (155)
17	GNOMAD	ss4225600591	Apr 26, 2021 (155)
18	GNOMAD	ss4225600592	Apr 26, 2021 (155)
19	GNOMAD	ss4225600593	Apr 26, 2021 (155)
20	GNOMAD	ss4225600594	Apr 26, 2021 (155)
21	TOMMO_GENOMICS	ss5199476776	Apr 26, 2021 (155)
22	TOMMO_GENOMICS	ss5199476777	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5199476778	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5199476779	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5199476780	Apr 26, 2021 (155)
26	1000G_HIGH_COVERAGE	ss5285468224	Oct 16, 2022 (156)
27	1000G_HIGH_COVERAGE	ss5285468225	Oct 16, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5285468226	Oct 16, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5285468227	Oct 16, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5285468228	Oct 16, 2022 (156)
31	HUGCELL_USP	ss5480891228	Oct 16, 2022 (156)
32	HUGCELL_USP	ss5480891229	Oct 16, 2022 (156)
33	HUGCELL_USP	ss5480891230	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5480891231	Oct 16, 2022 (156)
35	TOMMO_GENOMICS	ss5745847473	Oct 16, 2022 (156)
36	TOMMO_GENOMICS	ss5745847474	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5745847475	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5745847476	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5745847478	Oct 16, 2022 (156)
40	EVA	ss5849740260	Oct 16, 2022 (156)
41	1000Genomes	NC_000010.10 - 112345049	Oct 12, 2018 (152)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 363992730 (NC_000010.11:110585290::T 1329/113674) Row 363992731 (NC_000010.11:110585290::TT 7956/113606) Row 363992732 (NC_000010.11:110585290::TTT 4340/113658)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 363992730 (NC_000010.11:110585290::T 1329/113674) Row 363992731 (NC_000010.11:110585290::TT 7956/113606) Row 363992732 (NC_000010.11:110585290::TTT 4340/113658)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 363992730 (NC_000010.11:110585290::T 1329/113674) Row 363992731 (NC_000010.11:110585290::TT 7956/113606) Row 363992732 (NC_000010.11:110585290::TTT 4340/113658)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 363992730 (NC_000010.11:110585290::T 1329/113674) Row 363992731 (NC_000010.11:110585290::TT 7956/113606) Row 363992732 (NC_000010.11:110585290::TTT 4340/113658)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 363992730 (NC_000010.11:110585290::T 1329/113674) Row 363992731 (NC_000010.11:110585290::TT 7956/113606) Row 363992732 (NC_000010.11:110585290::TTT 4340/113658)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 363992730 (NC_000010.11:110585290::T 1329/113674) Row 363992731 (NC_000010.11:110585290::TT 7956/113606) Row 363992732 (NC_000010.11:110585290::TTT 4340/113658)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 363992730 (NC_000010.11:110585290::T 1329/113674) Row 363992731 (NC_000010.11:110585290::TT 7956/113606) Row 363992732 (NC_000010.11:110585290::TTT 4340/113658)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 363992730 (NC_000010.11:110585290::T 1329/113674) Row 363992731 (NC_000010.11:110585290::TT 7956/113606) Row 363992732 (NC_000010.11:110585290::TTT 4340/113658)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 363992730 (NC_000010.11:110585290::T 1329/113674) Row 363992731 (NC_000010.11:110585290::TT 7956/113606) Row 363992732 (NC_000010.11:110585290::TTT 4340/113658)...	-	Apr 26, 2021 (155)
51	Northern Sweden Submission ignored due to conflicting rows: Row 10964604 (NC_000010.10:112345048::TTT 17/600) Row 10964605 (NC_000010.10:112345048::TT 20/600)	-	Jul 13, 2019 (153)
52	Northern Sweden Submission ignored due to conflicting rows: Row 10964604 (NC_000010.10:112345048::TTT 17/600) Row 10964605 (NC_000010.10:112345048::TT 20/600)	-	Jul 13, 2019 (153)
53	8.3KJPN Submission ignored due to conflicting rows: Row 57446083 (NC_000010.10:112345048::TT 5144/16746) Row 57446084 (NC_000010.10:112345048::T 554/16746) Row 57446085 (NC_000010.10:112345048:T: 19/16746)...	-	Apr 26, 2021 (155)
54	8.3KJPN Submission ignored due to conflicting rows: Row 57446083 (NC_000010.10:112345048::TT 5144/16746) Row 57446084 (NC_000010.10:112345048::T 554/16746) Row 57446085 (NC_000010.10:112345048:T: 19/16746)...	-	Apr 26, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 57446083 (NC_000010.10:112345048::TT 5144/16746) Row 57446084 (NC_000010.10:112345048::T 554/16746) Row 57446085 (NC_000010.10:112345048:T: 19/16746)...	-	Apr 26, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 57446083 (NC_000010.10:112345048::TT 5144/16746) Row 57446084 (NC_000010.10:112345048::T 554/16746) Row 57446085 (NC_000010.10:112345048:T: 19/16746)...	-	Apr 26, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 57446083 (NC_000010.10:112345048::TT 5144/16746) Row 57446084 (NC_000010.10:112345048::T 554/16746) Row 57446085 (NC_000010.10:112345048:T: 19/16746)...	-	Apr 26, 2021 (155)
58	14KJPN Submission ignored due to conflicting rows: Row 79684577 (NC_000010.11:110585290::TT 8440/28182) Row 79684578 (NC_000010.11:110585290::T 899/28182) Row 79684579 (NC_000010.11:110585290:T: 22/28182)...	-	Oct 16, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 79684577 (NC_000010.11:110585290::TT 8440/28182) Row 79684578 (NC_000010.11:110585290::T 899/28182) Row 79684579 (NC_000010.11:110585290:T: 22/28182)...	-	Oct 16, 2022 (156)
60	14KJPN Submission ignored due to conflicting rows: Row 79684577 (NC_000010.11:110585290::TT 8440/28182) Row 79684578 (NC_000010.11:110585290::T 899/28182) Row 79684579 (NC_000010.11:110585290:T: 22/28182)...	-	Oct 16, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 79684577 (NC_000010.11:110585290::TT 8440/28182) Row 79684578 (NC_000010.11:110585290::T 899/28182) Row 79684579 (NC_000010.11:110585290:T: 22/28182)...	-	Oct 16, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 79684577 (NC_000010.11:110585290::TT 8440/28182) Row 79684578 (NC_000010.11:110585290::T 899/28182) Row 79684579 (NC_000010.11:110585290:T: 22/28182)...	-	Oct 16, 2022 (156)
63	ALFA	NC_000010.11 - 110585291	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
15129519217	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
15129519217	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4225600594	NC_000010.11:110585290:TTTTT:	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
15129519217	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4225600593	NC_000010.11:110585290:TTT:	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4225600592, ss5285468226	NC_000010.11:110585290:TT:	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
15129519217	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
51508857, ss1370100948, ss3786786122, ss5199476778	NC_000010.10:112345048:T:	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3813963106, ss4225600591, ss5285468225, ss5480891228, ss5745847475, ss5849740260	NC_000010.11:110585290:T:	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
15129519217	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss193204818	NT_030059.14:68891769:T:	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3007148705, ss5199476777	NC_000010.10:112345048::T	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4225600585, ss5285468228, ss5480891229, ss5745847474	NC_000010.11:110585290::T	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
15129519217	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3007148703, ss3737679740, ss5199476776	NC_000010.10:112345048::TT	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4225600586, ss5285468224, ss5480891230, ss5745847473	NC_000010.11:110585290::TT	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
15129519217	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3007148704, ss3737679739, ss3832332500, ss5199476779	NC_000010.10:112345048::TTT	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss947266795	NC_000010.10:112345049::TTT	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4225600587, ss5285468227, ss5480891231, ss5745847476	NC_000010.11:110585290::TTT	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
15129519217	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4225600588	NC_000010.11:110585290::TTTT	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
15129519217	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5199476780	NC_000010.10:112345048::TTTTT	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4225600589, ss5745847478	NC_000010.11:110585290::TTTTT	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3130441908	NC_000010.11:110585290:TTTTTTT:	NC_000010.11:110585290:TTTTTTTTTTT… NC_000010.11:110585290:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT

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

No publications for rs111694406

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

rs111694406