Name: rs144399770
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.

rs144399770

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:114148326-114148338 (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: delGGCT / dupGGCT / dup(GGCT)₂ / d…
delGGCT / dupGGCT / dup(GGCT)₂ / dup(GGCT)₃
Variation Type: Indel Insertion and Deletion
Frequency: dupGGCT=0.08042 (824/10246, ALFA)
dupGGCT=0.28 (11/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZBTB16 : 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	10246	TGGCTGGCTGGCT=0.90386	TGGCTGGCT=0.01571, TGGCTGGCTGGCTGGCT=0.08042, TGGCTGGCTGGCTGGCTGGCT=0.00000, TGGCTGGCTGGCTGGCTGGCTGGCT=0.00000	0.873868	0.034198	0.091933	32
European	Sub	8478	TGGCTGGCTGGCT=0.8838	TGGCTGGCT=0.0190, TGGCTGGCTGGCTGGCT=0.0972, TGGCTGGCTGGCTGGCTGGCT=0.0000, TGGCTGGCTGGCTGGCTGGCTGGCT=0.0000	0.846587	0.041595	0.111818	32
African	Sub	996	TGGCTGGCTGGCT=1.000	TGGCTGGCT=0.000, TGGCTGGCTGGCTGGCT=0.000, TGGCTGGCTGGCTGGCTGGCT=0.000, TGGCTGGCTGGCTGGCTGGCTGGCT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	34	TGGCTGGCTGGCT=1.00	TGGCTGGCT=0.00, TGGCTGGCTGGCTGGCT=0.00, TGGCTGGCTGGCTGGCTGGCT=0.00, TGGCTGGCTGGCTGGCTGGCTGGCT=0.00	1.0	0.0	0.0	N/A
African American	Sub	962	TGGCTGGCTGGCT=1.000	TGGCTGGCT=0.000, TGGCTGGCTGGCTGGCT=0.000, TGGCTGGCTGGCTGGCTGGCT=0.000, TGGCTGGCTGGCTGGCTGGCTGGCT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	72	TGGCTGGCTGGCT=1.00	TGGCTGGCT=0.00, TGGCTGGCTGGCTGGCT=0.00, TGGCTGGCTGGCTGGCTGGCT=0.00, TGGCTGGCTGGCTGGCTGGCTGGCT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	60	TGGCTGGCTGGCT=1.00	TGGCTGGCT=0.00, TGGCTGGCTGGCTGGCT=0.00, TGGCTGGCTGGCTGGCTGGCT=0.00, TGGCTGGCTGGCTGGCTGGCTGGCT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	12	TGGCTGGCTGGCT=1.00	TGGCTGGCT=0.00, TGGCTGGCTGGCTGGCT=0.00, TGGCTGGCTGGCTGGCTGGCT=0.00, TGGCTGGCTGGCTGGCTGGCTGGCT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	68	TGGCTGGCTGGCT=1.00	TGGCTGGCT=0.00, TGGCTGGCTGGCTGGCT=0.00, TGGCTGGCTGGCTGGCTGGCT=0.00, TGGCTGGCTGGCTGGCTGGCTGGCT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	342	TGGCTGGCTGGCT=1.000	TGGCTGGCT=0.000, TGGCTGGCTGGCTGGCT=0.000, TGGCTGGCTGGCTGGCTGGCT=0.000, TGGCTGGCTGGCTGGCTGGCTGGCT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	54	TGGCTGGCTGGCT=1.00	TGGCTGGCT=0.00, TGGCTGGCTGGCTGGCT=0.00, TGGCTGGCTGGCTGGCTGGCT=0.00, TGGCTGGCTGGCTGGCTGGCTGGCT=0.00	1.0	0.0	0.0	N/A
Other	Sub	236	TGGCTGGCTGGCT=1.000	TGGCTGGCT=0.000, TGGCTGGCTGGCTGGCT=0.000, TGGCTGGCTGGCTGGCTGGCT=0.000, TGGCTGGCTGGCTGGCTGGCTGGCT=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	10246	(TGGC)₃T=0.90386	delGGCT=0.01571, dupGGCT=0.08042, dup(GGCT)₂=0.00000, dup(GGCT)₃=0.00000
Allele Frequency Aggregator	European	Sub	8478	(TGGC)₃T=0.8838	delGGCT=0.0190, dupGGCT=0.0972, dup(GGCT)₂=0.0000, dup(GGCT)₃=0.0000
Allele Frequency Aggregator	African	Sub	996	(TGGC)₃T=1.000	delGGCT=0.000, dupGGCT=0.000, dup(GGCT)₂=0.000, dup(GGCT)₃=0.000
Allele Frequency Aggregator	Latin American 2	Sub	342	(TGGC)₃T=1.000	delGGCT=0.000, dupGGCT=0.000, dup(GGCT)₂=0.000, dup(GGCT)₃=0.000
Allele Frequency Aggregator	Other	Sub	236	(TGGC)₃T=1.000	delGGCT=0.000, dupGGCT=0.000, dup(GGCT)₂=0.000, dup(GGCT)₃=0.000
Allele Frequency Aggregator	Asian	Sub	72	(TGGC)₃T=1.00	delGGCT=0.00, dupGGCT=0.00, dup(GGCT)₂=0.00, dup(GGCT)₃=0.00
Allele Frequency Aggregator	Latin American 1	Sub	68	(TGGC)₃T=1.00	delGGCT=0.00, dupGGCT=0.00, dup(GGCT)₂=0.00, dup(GGCT)₃=0.00
Allele Frequency Aggregator	South Asian	Sub	54	(TGGC)₃T=1.00	delGGCT=0.00, dupGGCT=0.00, dup(GGCT)₂=0.00, dup(GGCT)₃=0.00
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupGGCT=0.28

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 11	NC_000011.10:g.114148327GGCT[2]
GRCh38.p14 chr 11	NC_000011.10:g.114148327GGCT[4]
GRCh38.p14 chr 11	NC_000011.10:g.114148327GGCT[5]
GRCh38.p14 chr 11	NC_000011.10:g.114148327GGCT[6]
GRCh37.p13 chr 11	NC_000011.9:g.114019049GGCT[2]
GRCh37.p13 chr 11	NC_000011.9:g.114019049GGCT[4]
GRCh37.p13 chr 11	NC_000011.9:g.114019049GGCT[5]
GRCh37.p13 chr 11	NC_000011.9:g.114019049GGCT[6]
ZBTB16 RefSeqGene	NG_012140.2:g.93752GGCT[2]
ZBTB16 RefSeqGene	NG_012140.2:g.93752GGCT[4]
ZBTB16 RefSeqGene	NG_012140.2:g.93752GGCT[5]
ZBTB16 RefSeqGene	NG_012140.2:g.93752GGCT[6]

Gene: ZBTB16, zinc finger and BTB domain containing 16 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZBTB16 transcript variant 2	NM_001018011.3:c.1269-801… NM_001018011.3:c.1269-8011TGGC[2]	N/A	Intron Variant
ZBTB16 transcript variant 3	NM_001354750.2:c.1269-801… NM_001354750.2:c.1269-8011TGGC[2]	N/A	Intron Variant
ZBTB16 transcript variant 4	NM_001354751.2:c.1269-801… NM_001354751.2:c.1269-8011TGGC[2]	N/A	Intron Variant
ZBTB16 transcript variant 5	NM_001354752.1:c.1269-801… NM_001354752.1:c.1269-8011TGGC[2]	N/A	Intron Variant
ZBTB16 transcript variant 1	NM_006006.6:c.1269-8011TG… NM_006006.6:c.1269-8011TGGC[2]	N/A	Intron Variant
ZBTB16 transcript variant X1	XM_005271658.6:c.1269-801… XM_005271658.6:c.1269-8011TGGC[2]	N/A	Intron Variant
ZBTB16 transcript variant X2	XM_047427563.1:c.	N/A	Genic Downstream 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	(TGGC)₃T=	delGGCT	dupGGCT	dup(GGCT)₂	dup(GGCT)₃
GRCh38.p14 chr 11	NC_000011.10:g.114148326_114148338=	NC_000011.10:g.114148327GGCT[2]	NC_000011.10:g.114148327GGCT[4]	NC_000011.10:g.114148327GGCT[5]	NC_000011.10:g.114148327GGCT[6]
GRCh37.p13 chr 11	NC_000011.9:g.114019048_114019060=	NC_000011.9:g.114019049GGCT[2]	NC_000011.9:g.114019049GGCT[4]	NC_000011.9:g.114019049GGCT[5]	NC_000011.9:g.114019049GGCT[6]
ZBTB16 RefSeqGene	NG_012140.2:g.93751_93763=	NG_012140.2:g.93752GGCT[2]	NG_012140.2:g.93752GGCT[4]	NG_012140.2:g.93752GGCT[5]	NG_012140.2:g.93752GGCT[6]
ZBTB16 transcript variant 2	NM_001018011.1:c.1269-8011=	NM_001018011.1:c.1269-8011TGGC[2]	NM_001018011.1:c.1269-8011TGGC[4]	NM_001018011.1:c.1269-8011TGGC[5]	NM_001018011.1:c.1269-8011TGGC[6]
ZBTB16 transcript variant 2	NM_001018011.3:c.1269-8011=	NM_001018011.3:c.1269-8011TGGC[2]	NM_001018011.3:c.1269-8011TGGC[4]	NM_001018011.3:c.1269-8011TGGC[5]	NM_001018011.3:c.1269-8011TGGC[6]
ZBTB16 transcript variant 3	NM_001354750.2:c.1269-8011=	NM_001354750.2:c.1269-8011TGGC[2]	NM_001354750.2:c.1269-8011TGGC[4]	NM_001354750.2:c.1269-8011TGGC[5]	NM_001354750.2:c.1269-8011TGGC[6]
ZBTB16 transcript variant 4	NM_001354751.2:c.1269-8011=	NM_001354751.2:c.1269-8011TGGC[2]	NM_001354751.2:c.1269-8011TGGC[4]	NM_001354751.2:c.1269-8011TGGC[5]	NM_001354751.2:c.1269-8011TGGC[6]
ZBTB16 transcript variant 5	NM_001354752.1:c.1269-8011=	NM_001354752.1:c.1269-8011TGGC[2]	NM_001354752.1:c.1269-8011TGGC[4]	NM_001354752.1:c.1269-8011TGGC[5]	NM_001354752.1:c.1269-8011TGGC[6]
ZBTB16 transcript variant 1	NM_006006.4:c.1269-8011=	NM_006006.4:c.1269-8011TGGC[2]	NM_006006.4:c.1269-8011TGGC[4]	NM_006006.4:c.1269-8011TGGC[5]	NM_006006.4:c.1269-8011TGGC[6]
ZBTB16 transcript variant 1	NM_006006.6:c.1269-8011=	NM_006006.6:c.1269-8011TGGC[2]	NM_006006.6:c.1269-8011TGGC[4]	NM_006006.6:c.1269-8011TGGC[5]	NM_006006.6:c.1269-8011TGGC[6]
ZBTB16 transcript variant X1	XM_005271657.1:c.1269-8011=	XM_005271657.1:c.1269-8011TGGC[2]	XM_005271657.1:c.1269-8011TGGC[4]	XM_005271657.1:c.1269-8011TGGC[5]	XM_005271657.1:c.1269-8011TGGC[6]
ZBTB16 transcript variant X2	XM_005271658.1:c.1269-8011=	XM_005271658.1:c.1269-8011TGGC[2]	XM_005271658.1:c.1269-8011TGGC[4]	XM_005271658.1:c.1269-8011TGGC[5]	XM_005271658.1:c.1269-8011TGGC[6]
ZBTB16 transcript variant X1	XM_005271658.6:c.1269-8011=	XM_005271658.6:c.1269-8011TGGC[2]	XM_005271658.6:c.1269-8011TGGC[4]	XM_005271658.6:c.1269-8011TGGC[5]	XM_005271658.6:c.1269-8011TGGC[6]

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#.

46 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	1000GENOMES	ss327382714	May 09, 2011 (134)
2	1000GENOMES	ss327473104	May 09, 2011 (134)
3	1000GENOMES	ss327897852	Jan 10, 2018 (151)
4	LUNTER	ss552167840	Apr 25, 2013 (138)
5	LUNTER	ss552434813	Apr 25, 2013 (138)
6	LUNTER	ss553465911	Apr 25, 2013 (138)
7	SSMP	ss664024100	Apr 01, 2015 (144)
8	EVA_GENOME_DK	ss1574419250	Apr 01, 2015 (144)
9	EVA_DECODE	ss1598649829	Apr 01, 2015 (144)
10	EVA_DECODE	ss1598649830	Oct 12, 2018 (152)
11	EVA_DECODE	ss1598649831	Apr 01, 2015 (144)
12	EVA_DECODE	ss1598649832	Apr 01, 2015 (144)
13	EVA_DECODE	ss1598649833	Apr 01, 2015 (144)
14	EVA_UK10K_ALSPAC	ss1707265453	Apr 01, 2015 (144)
15	EVA_UK10K_TWINSUK	ss1707265486	Apr 01, 2015 (144)
16	EVA_UK10K_TWINSUK	ss1710533524	Oct 12, 2018 (152)
17	EVA_UK10K_ALSPAC	ss1710533544	Oct 12, 2018 (152)
18	SWEGEN	ss3008811757	Nov 08, 2017 (151)
19	MCHAISSO	ss3063708638	Jan 10, 2018 (151)
20	MCHAISSO	ss3064535236	Jan 10, 2018 (151)
21	MCHAISSO	ss3065450209	Jan 10, 2018 (151)
22	BEROUKHIMLAB	ss3644329563	Oct 12, 2018 (152)
23	URBANLAB	ss3649709243	Oct 12, 2018 (152)
24	EVA_DECODE	ss3692637593	Jul 13, 2019 (153)
25	EVA_DECODE	ss3692637594	Jul 13, 2019 (153)
26	EVA_DECODE	ss3692637595	Jul 13, 2019 (153)
27	ACPOP	ss3738557016	Jul 13, 2019 (153)
28	ACPOP	ss3738557017	Jul 13, 2019 (153)
29	KOGIC	ss3970787093	Apr 26, 2020 (154)
30	KOGIC	ss3970787094	Apr 26, 2020 (154)
31	GNOMAD	ss4242918112	Apr 26, 2021 (155)
32	GNOMAD	ss4242918113	Apr 26, 2021 (155)
33	GNOMAD	ss4242918114	Apr 26, 2021 (155)
34	GNOMAD	ss4242918115	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5203977705	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5203977706	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5203977707	Apr 26, 2021 (155)
38	1000G_HIGH_COVERAGE	ss5288971167	Oct 16, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5288971168	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5483953683	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5483953684	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5752451161	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5752451162	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5752451163	Oct 16, 2022 (156)
45	EVA	ss5837256615	Oct 16, 2022 (156)
46	EVA	ss5837256616	Oct 16, 2022 (156)
47	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 30879306 (NC_000011.9:114019047::TGGC 2705/3854) Row 30879307 (NC_000011.9:114019047:TGGC: 465/3854)	-	Oct 12, 2018 (152)
48	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 30879306 (NC_000011.9:114019047::TGGC 2705/3854) Row 30879307 (NC_000011.9:114019047:TGGC: 465/3854)	-	Oct 12, 2018 (152)
49	The Danish reference pan genome	NC_000011.9 - 114019048	Apr 26, 2020 (154)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392541215 (NC_000011.10:114148325::TGGC 16912/83732) Row 392541216 (NC_000011.10:114148325::TGGCTGGC 7/84534) Row 392541217 (NC_000011.10:114148325::TGGCTGGCTGGC 1/84534)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392541215 (NC_000011.10:114148325::TGGC 16912/83732) Row 392541216 (NC_000011.10:114148325::TGGCTGGC 7/84534) Row 392541217 (NC_000011.10:114148325::TGGCTGGCTGGC 1/84534)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392541215 (NC_000011.10:114148325::TGGC 16912/83732) Row 392541216 (NC_000011.10:114148325::TGGCTGGC 7/84534) Row 392541217 (NC_000011.10:114148325::TGGCTGGCTGGC 1/84534)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392541215 (NC_000011.10:114148325::TGGC 16912/83732) Row 392541216 (NC_000011.10:114148325::TGGCTGGC 7/84534) Row 392541217 (NC_000011.10:114148325::TGGCTGGCTGGC 1/84534)...	-	Apr 26, 2021 (155)
54	Korean Genome Project Submission ignored due to conflicting rows: Row 27165094 (NC_000011.10:114148329::TGGC 293/1828) Row 27165095 (NC_000011.10:114148325:TGGC: 11/1828)	-	Apr 26, 2020 (154)
55	Korean Genome Project Submission ignored due to conflicting rows: Row 27165094 (NC_000011.10:114148329::TGGC 293/1828) Row 27165095 (NC_000011.10:114148325:TGGC: 11/1828)	-	Apr 26, 2020 (154)
56	Northern Sweden Submission ignored due to conflicting rows: Row 11841881 (NC_000011.9:114019047::TGGC 131/590) Row 11841882 (NC_000011.9:114019047:TGGC: 25/590)	-	Jul 13, 2019 (153)
57	Northern Sweden Submission ignored due to conflicting rows: Row 11841881 (NC_000011.9:114019047::TGGC 131/590) Row 11841882 (NC_000011.9:114019047:TGGC: 25/590)	-	Jul 13, 2019 (153)
58	8.3KJPN Submission ignored due to conflicting rows: Row 61947012 (NC_000011.9:114019047::TGGC 3042/16618) Row 61947013 (NC_000011.9:114019047:TGGC: 210/16618) Row 61947014 (NC_000011.9:114019047::TGGCTGGC 1/16618)	-	Apr 26, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 61947012 (NC_000011.9:114019047::TGGC 3042/16618) Row 61947013 (NC_000011.9:114019047:TGGC: 210/16618) Row 61947014 (NC_000011.9:114019047::TGGCTGGC 1/16618)	-	Apr 26, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 61947012 (NC_000011.9:114019047::TGGC 3042/16618) Row 61947013 (NC_000011.9:114019047:TGGC: 210/16618) Row 61947014 (NC_000011.9:114019047::TGGCTGGC 1/16618)	-	Apr 26, 2021 (155)
61	14KJPN Submission ignored due to conflicting rows: Row 86288265 (NC_000011.10:114148325::TGGC 4526/28064) Row 86288266 (NC_000011.10:114148325:TGGC: 385/28064) Row 86288267 (NC_000011.10:114148325::TGGCTGGC 1/28064)	-	Oct 16, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 86288265 (NC_000011.10:114148325::TGGC 4526/28064) Row 86288266 (NC_000011.10:114148325:TGGC: 385/28064) Row 86288267 (NC_000011.10:114148325::TGGCTGGC 1/28064)	-	Oct 16, 2022 (156)
63	14KJPN Submission ignored due to conflicting rows: Row 86288265 (NC_000011.10:114148325::TGGC 4526/28064) Row 86288266 (NC_000011.10:114148325:TGGC: 385/28064) Row 86288267 (NC_000011.10:114148325::TGGCTGGC 1/28064)	-	Oct 16, 2022 (156)
64	UK 10K study - Twins Submission ignored due to conflicting rows: Row 30879306 (NC_000011.9:114019047::TGGC 2605/3708) Row 30879307 (NC_000011.9:114019047:TGGC: 415/3708)	-	Oct 12, 2018 (152)
65	UK 10K study - Twins Submission ignored due to conflicting rows: Row 30879306 (NC_000011.9:114019047::TGGC 2605/3708) Row 30879307 (NC_000011.9:114019047:TGGC: 415/3708)	-	Oct 12, 2018 (152)
66	ALFA	NC_000011.10 - 114148326	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
ss327897852, ss552434813	NC_000011.8:113524257:TGGC:	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCT	(self)
ss664024100, ss1707265453, ss1707265486, ss3008811757, ss3738557017, ss5203977706, ss5837256616	NC_000011.9:114019047:TGGC:	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCT	(self)
ss3692637593, ss3970787094, ss4242918115, ss5288971168, ss5483953683, ss5752451162	NC_000011.10:114148325:TGGC:	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCT	(self)
9320782837	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCT	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCT	(self)
ss327382714, ss327473104, ss552167840, ss553465911	NC_000011.8:113524257::TGGC	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCTGGCTGGCT	(self)
ss1598649829	NC_000011.8:113524258::GGCT	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCTGGCTGGCT	(self)
ss1598649830	NC_000011.8:113524259::GCTG	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCTGGCTGGCT	(self)
ss1598649831	NC_000011.8:113524260::CTGG	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCTGGCTGGCT	(self)
ss1598649832	NC_000011.8:113524265::TGGC	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCTGGCTGGCT	(self)
ss1598649833	NC_000011.8:113524266::GGCT	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCTGGCTGGCT	(self)
322176, ss1574419250, ss3644329563, ss3738557016, ss5203977705, ss5837256615	NC_000011.9:114019047::TGGC	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCTGGCTGGCT	(self)
ss1710533524, ss1710533544	NC_000011.9:114019051::TGGC	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCTGGCTGGCT	(self)
ss3063708638, ss3064535236, ss3065450209, ss3649709243, ss4242918112, ss5288971167, ss5483953684, ss5752451161	NC_000011.10:114148325::TGGC	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCTGGCTGGCT	(self)
9320782837	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCTGGCTGGCT	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCTGGCTGGCT	(self)
ss3692637594, ss3970787093	NC_000011.10:114148329::TGGC	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCTGGCTGGCT	(self)
ss5203977707	NC_000011.9:114019047::TGGCTGGC	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCTGGCTGGCTGGCT	(self)
ss4242918113, ss5752451163	NC_000011.10:114148325::TGGCTGGC	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCTGGCTGGCTGGCT	(self)
9320782837	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCTGGCTGGCTGGCT	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCTGGCTGGCTGGCT	(self)
ss3692637595	NC_000011.10:114148329::TGGCTGGC	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCTGGCTGGCTGGCT	(self)
ss4242918114	NC_000011.10:114148325::TGGCTGGCTG… NC_000011.10:114148325::TGGCTGGCTGGC	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCTGGCTGGCTGGCTGGCT	(self)
9320782837	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCTGGCTGGCTGGCTGGCT	NC_000011.10:114148325:TGGCTGGCTGG… NC_000011.10:114148325:TGGCTGGCTGGCT:TGGCTGGCTGGCTGGCTGGCTGGCT	(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 rs144399770

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).
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs144399770