Name: rs1555163170
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.

rs1555163170

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:49191712-49191738 (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(CT)₆ / del(CT)₅ / del(CT)₄ / d…
del(CT)₆ / del(CT)₅ / del(CT)₄ / del(CT)₃ / delCTCT / delCT / dupCT / dupCTCT / dup(CT)₃ / dup(CT)₄ / dup(CT)₅ / dup(CT)₆
Variation Type: Indel Insertion and Deletion
Frequency: dupCT=0.3165 (1981/6259, ALFA)
(TC)₁₃T=0.1513 (583/3854, ALSPAC)
(TC)₁₃T=0.1583 (587/3708, TWINSUK) (+ 2 more)
(TC)₁₃T=0.5 (4/8, KOREAN)
dupCT=0.5 (4/8, KOREAN)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
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	6259	TCTCTCTCTCTCTCTCTCTCTCTCTCT=0.5509	TCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCT=0.0687, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.3165, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0272, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0356, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0011, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000	0.51617	0.183404	0.300426	32
European	Sub	5445	TCTCTCTCTCTCTCTCTCTCTCTCTCT=0.4843	TCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCT=0.0788, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.3635, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0312, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0410, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0013, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000	0.415638	0.221193	0.363169	32
African	Sub	536	TCTCTCTCTCTCTCTCTCTCTCTCTCT=1.000	TCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	22	TCTCTCTCTCTCTCTCTCTCTCTCTCT=1.00	TCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	1.0	0.0	0.0	N/A
African American	Sub	514	TCTCTCTCTCTCTCTCTCTCTCTCTCT=1.000	TCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	66	TCTCTCTCTCTCTCTCTCTCTCTCTCT=1.00	TCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	50	TCTCTCTCTCTCTCTCTCTCTCTCTCT=1.00	TCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	16	TCTCTCTCTCTCTCTCTCTCTCTCTCT=1.00	TCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	28	TCTCTCTCTCTCTCTCTCTCTCTCTCT=1.00	TCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	76	TCTCTCTCTCTCTCTCTCTCTCTCTCT=1.00	TCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	24	TCTCTCTCTCTCTCTCTCTCTCTCTCT=1.00	TCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	1.0	0.0	0.0	N/A
Other	Sub	84	TCTCTCTCTCTCTCTCTCTCTCTCTCT=0.96	TCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCT=0.01, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.02, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	0.97561	0.02439	0.0	22

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	6259	(TC)₁₃T=0.5509	del(CT)₆=0.0000, del(CT)₅=0.0000, del(CT)₄=0.0000, del(CT)₃=0.0000, delCTCT=0.0000, delCT=0.0687, dupCT=0.3165, dupCTCT=0.0272, dup(CT)₃=0.0356, dup(CT)₄=0.0011, dup(CT)₅=0.0000, dup(CT)₆=0.0000
Allele Frequency Aggregator	European	Sub	5445	(TC)₁₃T=0.4843	del(CT)₆=0.0000, del(CT)₅=0.0000, del(CT)₄=0.0000, del(CT)₃=0.0000, delCTCT=0.0000, delCT=0.0788, dupCT=0.3635, dupCTCT=0.0312, dup(CT)₃=0.0410, dup(CT)₄=0.0013, dup(CT)₅=0.0000, dup(CT)₆=0.0000
Allele Frequency Aggregator	African	Sub	536	(TC)₁₃T=1.000	del(CT)₆=0.000, del(CT)₅=0.000, del(CT)₄=0.000, del(CT)₃=0.000, delCTCT=0.000, delCT=0.000, dupCT=0.000, dupCTCT=0.000, dup(CT)₃=0.000, dup(CT)₄=0.000, dup(CT)₅=0.000, dup(CT)₆=0.000
Allele Frequency Aggregator	Other	Sub	84	(TC)₁₃T=0.96	del(CT)₆=0.00, del(CT)₅=0.00, del(CT)₄=0.00, del(CT)₃=0.00, delCTCT=0.00, delCT=0.01, dupCT=0.02, dupCTCT=0.00, dup(CT)₃=0.00, dup(CT)₄=0.00, dup(CT)₅=0.00, dup(CT)₆=0.00
Allele Frequency Aggregator	Latin American 2	Sub	76	(TC)₁₃T=1.00	del(CT)₆=0.00, del(CT)₅=0.00, del(CT)₄=0.00, del(CT)₃=0.00, delCTCT=0.00, delCT=0.00, dupCT=0.00, dupCTCT=0.00, dup(CT)₃=0.00, dup(CT)₄=0.00, dup(CT)₅=0.00, dup(CT)₆=0.00
Allele Frequency Aggregator	Asian	Sub	66	(TC)₁₃T=1.00	del(CT)₆=0.00, del(CT)₅=0.00, del(CT)₄=0.00, del(CT)₃=0.00, delCTCT=0.00, delCT=0.00, dupCT=0.00, dupCTCT=0.00, dup(CT)₃=0.00, dup(CT)₄=0.00, dup(CT)₅=0.00, dup(CT)₆=0.00
Allele Frequency Aggregator	Latin American 1	Sub	28	(TC)₁₃T=1.00	del(CT)₆=0.00, del(CT)₅=0.00, del(CT)₄=0.00, del(CT)₃=0.00, delCTCT=0.00, delCT=0.00, dupCT=0.00, dupCTCT=0.00, dup(CT)₃=0.00, dup(CT)₄=0.00, dup(CT)₅=0.00, dup(CT)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	24	(TC)₁₃T=1.00	del(CT)₆=0.00, del(CT)₅=0.00, del(CT)₄=0.00, del(CT)₃=0.00, delCTCT=0.00, delCT=0.00, dupCT=0.00, dupCTCT=0.00, dup(CT)₃=0.00, dup(CT)₄=0.00, dup(CT)₅=0.00, dup(CT)₆=0.00
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	- No frequency provided	dupCT=0.8487
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	- No frequency provided	dupCT=0.8417
KOREAN population from KRGDB	KOREAN	Study-wide	8	- No frequency provided	dupCT=0.5

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 12	NC_000012.12:g.49191713CT[7]
GRCh38.p14 chr 12	NC_000012.12:g.49191713CT[8]
GRCh38.p14 chr 12	NC_000012.12:g.49191713CT[9]
GRCh38.p14 chr 12	NC_000012.12:g.49191713CT[10]
GRCh38.p14 chr 12	NC_000012.12:g.49191713CT[11]
GRCh38.p14 chr 12	NC_000012.12:g.49191713CT[12]
GRCh38.p14 chr 12	NC_000012.12:g.49191713CT[14]
GRCh38.p14 chr 12	NC_000012.12:g.49191713CT[15]
GRCh38.p14 chr 12	NC_000012.12:g.49191713CT[16]
GRCh38.p14 chr 12	NC_000012.12:g.49191713CT[17]
GRCh38.p14 chr 12	NC_000012.12:g.49191713CT[18]
GRCh38.p14 chr 12	NC_000012.12:g.49191713CT[19]
GRCh37.p13 chr 12	NC_000012.11:g.49585496CT[7]
GRCh37.p13 chr 12	NC_000012.11:g.49585496CT[8]
GRCh37.p13 chr 12	NC_000012.11:g.49585496CT[9]
GRCh37.p13 chr 12	NC_000012.11:g.49585496CT[10]
GRCh37.p13 chr 12	NC_000012.11:g.49585496CT[11]
GRCh37.p13 chr 12	NC_000012.11:g.49585496CT[12]
GRCh37.p13 chr 12	NC_000012.11:g.49585496CT[14]
GRCh37.p13 chr 12	NC_000012.11:g.49585496CT[15]
GRCh37.p13 chr 12	NC_000012.11:g.49585496CT[16]
GRCh37.p13 chr 12	NC_000012.11:g.49585496CT[17]
GRCh37.p13 chr 12	NC_000012.11:g.49585496CT[18]
GRCh37.p13 chr 12	NC_000012.11:g.49585496CT[19]
TUBA1A RefSeqGene	NG_008966.1:g.2342GA[7]
TUBA1A RefSeqGene	NG_008966.1:g.2342GA[8]
TUBA1A RefSeqGene	NG_008966.1:g.2342GA[9]
TUBA1A RefSeqGene	NG_008966.1:g.2342GA[10]
TUBA1A RefSeqGene	NG_008966.1:g.2342GA[11]
TUBA1A RefSeqGene	NG_008966.1:g.2342GA[12]
TUBA1A RefSeqGene	NG_008966.1:g.2342GA[14]
TUBA1A RefSeqGene	NG_008966.1:g.2342GA[15]
TUBA1A RefSeqGene	NG_008966.1:g.2342GA[16]
TUBA1A RefSeqGene	NG_008966.1:g.2342GA[17]
TUBA1A RefSeqGene	NG_008966.1:g.2342GA[18]
TUBA1A RefSeqGene	NG_008966.1:g.2342GA[19]

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	(TC)₁₃T=	del(CT)₆	del(CT)₅	del(CT)₄	del(CT)₃	delCTCT	delCT	dupCT	dupCTCT	dup(CT)₃	dup(CT)₄	dup(CT)₅	dup(CT)₆
GRCh38.p14 chr 12	NC_000012.12:g.49191712_49191738=	NC_000012.12:g.49191713CT[7]	NC_000012.12:g.49191713CT[8]	NC_000012.12:g.49191713CT[9]	NC_000012.12:g.49191713CT[10]	NC_000012.12:g.49191713CT[11]	NC_000012.12:g.49191713CT[12]	NC_000012.12:g.49191713CT[14]	NC_000012.12:g.49191713CT[15]	NC_000012.12:g.49191713CT[16]	NC_000012.12:g.49191713CT[17]	NC_000012.12:g.49191713CT[18]	NC_000012.12:g.49191713CT[19]
GRCh37.p13 chr 12	NC_000012.11:g.49585495_49585521=	NC_000012.11:g.49585496CT[7]	NC_000012.11:g.49585496CT[8]	NC_000012.11:g.49585496CT[9]	NC_000012.11:g.49585496CT[10]	NC_000012.11:g.49585496CT[11]	NC_000012.11:g.49585496CT[12]	NC_000012.11:g.49585496CT[14]	NC_000012.11:g.49585496CT[15]	NC_000012.11:g.49585496CT[16]	NC_000012.11:g.49585496CT[17]	NC_000012.11:g.49585496CT[18]	NC_000012.11:g.49585496CT[19]
TUBA1A RefSeqGene	NG_008966.1:g.2341_2367=	NG_008966.1:g.2342GA[7]	NG_008966.1:g.2342GA[8]	NG_008966.1:g.2342GA[9]	NG_008966.1:g.2342GA[10]	NG_008966.1:g.2342GA[11]	NG_008966.1:g.2342GA[12]	NG_008966.1:g.2342GA[14]	NG_008966.1:g.2342GA[15]	NG_008966.1:g.2342GA[16]	NG_008966.1:g.2342GA[17]	NG_008966.1:g.2342GA[18]	NG_008966.1:g.2342GA[19]

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#.

55 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80831693	Oct 12, 2018 (152)
2	HGSV	ss81553162	Aug 21, 2014 (142)
3	HGSV	ss82241883	Aug 21, 2014 (142)
4	BILGI_BIOE	ss666569129	Aug 21, 2014 (144)
5	DDI	ss1536726483	Apr 01, 2015 (144)
6	EVA_UK10K_ALSPAC	ss1707460275	Oct 12, 2018 (152)
7	EVA_UK10K_TWINSUK	ss1707460321	Oct 12, 2018 (152)
8	HAMMER_LAB	ss1807238071	Sep 08, 2015 (146)
9	MCHAISSO	ss3063728856	Jan 10, 2018 (151)
10	MCHAISSO	ss3064558020	Jan 10, 2018 (151)
11	MCHAISSO	ss3065475457	Jan 10, 2018 (151)
12	MCHAISSO	ss3065475458	Jan 10, 2018 (151)
13	EVA_DECODE	ss3693637865	Jul 13, 2019 (153)
14	EVA_DECODE	ss3693637866	Jul 13, 2019 (153)
15	EVA_DECODE	ss3693637867	Jul 13, 2019 (153)
16	EVA_DECODE	ss3693637868	Jul 13, 2019 (153)
17	EVA_DECODE	ss3693637869	Jul 13, 2019 (153)
18	EVA_DECODE	ss3693637870	Jul 13, 2019 (153)
19	ACPOP	ss3739008055	Jul 13, 2019 (153)
20	ACPOP	ss3739008056	Jul 13, 2019 (153)
21	ACPOP	ss3739008058	Jul 13, 2019 (153)
22	ACPOP	ss3739008059	Jul 13, 2019 (153)
23	PACBIO	ss3787221262	Jul 13, 2019 (153)
24	PACBIO	ss3792323863	Jul 13, 2019 (153)
25	PACBIO	ss3797206623	Jul 13, 2019 (153)
26	EVA	ss3833114723	Apr 27, 2020 (154)
27	EVA	ss3840127799	Apr 27, 2020 (154)
28	EVA	ss3845614087	Apr 27, 2020 (154)
29	KRGDB	ss3926863141	Apr 27, 2020 (154)
30	GNOMAD	ss4251504424	Apr 26, 2021 (155)
31	GNOMAD	ss4251504425	Apr 26, 2021 (155)
32	GNOMAD	ss4251504426	Apr 26, 2021 (155)
33	GNOMAD	ss4251504427	Apr 26, 2021 (155)
34	GNOMAD	ss4251504428	Apr 26, 2021 (155)
35	GNOMAD	ss4251504433	Apr 26, 2021 (155)
36	GNOMAD	ss4251504434	Apr 26, 2021 (155)
37	GNOMAD	ss4251504435	Apr 26, 2021 (155)
38	GNOMAD	ss4251504436	Apr 26, 2021 (155)
39	GNOMAD	ss4251504437	Apr 26, 2021 (155)
40	GNOMAD	ss4251504438	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5206239957	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5206239958	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5206239959	Apr 26, 2021 (155)
44	1000G_HIGH_COVERAGE	ss5290750145	Oct 13, 2022 (156)
45	HUGCELL_USP	ss5485509942	Oct 13, 2022 (156)
46	HUGCELL_USP	ss5485509944	Oct 13, 2022 (156)
47	HUGCELL_USP	ss5485509945	Oct 13, 2022 (156)
48	HUGCELL_USP	ss5485509946	Oct 13, 2022 (156)
49	HUGCELL_USP	ss5485509947	Oct 13, 2022 (156)
50	TOMMO_GENOMICS	ss5756003497	Oct 13, 2022 (156)
51	TOMMO_GENOMICS	ss5756003498	Oct 13, 2022 (156)
52	TOMMO_GENOMICS	ss5756003500	Oct 13, 2022 (156)
53	EVA	ss5837944773	Oct 13, 2022 (156)
54	EVA	ss5837944774	Oct 13, 2022 (156)
55	EVA	ss5850374918	Oct 13, 2022 (156)
56	The Avon Longitudinal Study of Parents and Children	NC_000012.11 - 49585522	Oct 12, 2018 (152)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406843407 (NC_000012.12:49191711::TC 53262/119296) Row 406843408 (NC_000012.12:49191711::TCTC 3106/119792) Row 406843409 (NC_000012.12:49191711::TCTCTC 2375/119802)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406843407 (NC_000012.12:49191711::TC 53262/119296) Row 406843408 (NC_000012.12:49191711::TCTC 3106/119792) Row 406843409 (NC_000012.12:49191711::TCTCTC 2375/119802)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406843407 (NC_000012.12:49191711::TC 53262/119296) Row 406843408 (NC_000012.12:49191711::TCTC 3106/119792) Row 406843409 (NC_000012.12:49191711::TCTCTC 2375/119802)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406843407 (NC_000012.12:49191711::TC 53262/119296) Row 406843408 (NC_000012.12:49191711::TCTC 3106/119792) Row 406843409 (NC_000012.12:49191711::TCTCTC 2375/119802)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406843407 (NC_000012.12:49191711::TC 53262/119296) Row 406843408 (NC_000012.12:49191711::TCTC 3106/119792) Row 406843409 (NC_000012.12:49191711::TCTCTC 2375/119802)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406843407 (NC_000012.12:49191711::TC 53262/119296) Row 406843408 (NC_000012.12:49191711::TCTC 3106/119792) Row 406843409 (NC_000012.12:49191711::TCTCTC 2375/119802)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406843407 (NC_000012.12:49191711::TC 53262/119296) Row 406843408 (NC_000012.12:49191711::TCTC 3106/119792) Row 406843409 (NC_000012.12:49191711::TCTCTC 2375/119802)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406843407 (NC_000012.12:49191711::TC 53262/119296) Row 406843408 (NC_000012.12:49191711::TCTC 3106/119792) Row 406843409 (NC_000012.12:49191711::TCTCTC 2375/119802)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406843407 (NC_000012.12:49191711::TC 53262/119296) Row 406843408 (NC_000012.12:49191711::TCTC 3106/119792) Row 406843409 (NC_000012.12:49191711::TCTCTC 2375/119802)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406843407 (NC_000012.12:49191711::TC 53262/119296) Row 406843408 (NC_000012.12:49191711::TCTC 3106/119792) Row 406843409 (NC_000012.12:49191711::TCTCTC 2375/119802)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406843407 (NC_000012.12:49191711::TC 53262/119296) Row 406843408 (NC_000012.12:49191711::TCTC 3106/119792) Row 406843409 (NC_000012.12:49191711::TCTCTC 2375/119802)...	-	Apr 26, 2021 (155)
68	KOREAN population from KRGDB	NC_000012.11 - 49585495	Apr 27, 2020 (154)
69	Northern Sweden Submission ignored due to conflicting rows: Row 12292920 (NC_000012.11:49585494::TC 322/600) Row 12292921 (NC_000012.11:49585494:TC: 40/600) Row 12292923 (NC_000012.11:49585494::TCTC 12/600)...	-	Jul 13, 2019 (153)
70	Northern Sweden Submission ignored due to conflicting rows: Row 12292920 (NC_000012.11:49585494::TC 322/600) Row 12292921 (NC_000012.11:49585494:TC: 40/600) Row 12292923 (NC_000012.11:49585494::TCTC 12/600)...	-	Jul 13, 2019 (153)
71	Northern Sweden Submission ignored due to conflicting rows: Row 12292920 (NC_000012.11:49585494::TC 322/600) Row 12292921 (NC_000012.11:49585494:TC: 40/600) Row 12292923 (NC_000012.11:49585494::TCTC 12/600)...	-	Jul 13, 2019 (153)
72	Northern Sweden Submission ignored due to conflicting rows: Row 12292920 (NC_000012.11:49585494::TC 322/600) Row 12292921 (NC_000012.11:49585494:TC: 40/600) Row 12292923 (NC_000012.11:49585494::TCTC 12/600)...	-	Jul 13, 2019 (153)
73	8.3KJPN Submission ignored due to conflicting rows: Row 64209264 (NC_000012.11:49585494::TC 4874/16760) Row 64209265 (NC_000012.11:49585494::TCTC 265/16760) Row 64209266 (NC_000012.11:49585494:TC: 77/16760)	-	Apr 26, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 64209264 (NC_000012.11:49585494::TC 4874/16760) Row 64209265 (NC_000012.11:49585494::TCTC 265/16760) Row 64209266 (NC_000012.11:49585494:TC: 77/16760)	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 64209264 (NC_000012.11:49585494::TC 4874/16760) Row 64209265 (NC_000012.11:49585494::TCTC 265/16760) Row 64209266 (NC_000012.11:49585494:TC: 77/16760)	-	Apr 26, 2021 (155)
76	14KJPN Submission ignored due to conflicting rows: Row 89840601 (NC_000012.12:49191711:TC: 134/26258) Row 89840602 (NC_000012.12:49191711::TC 7860/26258) Row 89840604 (NC_000012.12:49191711::TCTC 369/26258)	-	Oct 13, 2022 (156)
77	14KJPN Submission ignored due to conflicting rows: Row 89840601 (NC_000012.12:49191711:TC: 134/26258) Row 89840602 (NC_000012.12:49191711::TC 7860/26258) Row 89840604 (NC_000012.12:49191711::TCTC 369/26258)	-	Oct 13, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 89840601 (NC_000012.12:49191711:TC: 134/26258) Row 89840602 (NC_000012.12:49191711::TC 7860/26258) Row 89840604 (NC_000012.12:49191711::TCTC 369/26258)	-	Oct 13, 2022 (156)
79	UK 10K study - Twins	NC_000012.11 - 49585522	Oct 12, 2018 (152)
80	ALFA	NC_000012.12 - 49191712	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)
rs368130489	May 13, 2013 (138)
rs527823879	Apr 01, 2015 (144)
rs796714730	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4251504438	NC_000012.12:49191711:TCTCTCTCTCTC:	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCT	(self)
3933913635	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCT	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCT	(self)
ss4251504437	NC_000012.12:49191711:TCTCTCTCTC:	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCT	(self)
3933913635	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCT	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCT	(self)
ss4251504436	NC_000012.12:49191711:TCTCTCTC:	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCT	(self)
3933913635	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCT	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCT	(self)
ss3693637865, ss4251504435	NC_000012.12:49191711:TCTCTC:	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCT	(self)
3933913635	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCT	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCT	(self)
ss81553162, ss82241883	NC_000012.9:47871784:CTCT:	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCT	(self)
ss1807238071, ss3833114723	NC_000012.11:49585494:TCTC:	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCT	(self)
ss4251504434, ss5485509946	NC_000012.12:49191711:TCTC:	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCT	(self)
3933913635	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCT	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3693637866	NC_000012.12:49191713:TCTC:	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3739008056, ss3840127799, ss5206239959, ss5837944774	NC_000012.11:49585494:TC:	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3845614087, ss4251504433, ss5485509944, ss5756003497	NC_000012.12:49191711:TC:	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCT	(self)
3933913635	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCT	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3693637867	NC_000012.12:49191715:TC:	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCT	(self)
34040535, ss666569129, ss1536726483, ss3739008055, ss3787221262, ss3792323863, ss3797206623, ss3926863141, ss5206239957, ss5837944773	NC_000012.11:49585494::TC	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
32039110, 32039110, ss1707460275, ss1707460321	NC_000012.11:49585521::CT	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3063728856, ss3064558020, ss3065475457, ss3065475458, ss4251504424, ss5290750145, ss5485509942, ss5756003498, ss5850374918	NC_000012.12:49191711::TC	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
3933913635	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3693637868	NC_000012.12:49191717::TC	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss80831693	NT_029419.12:11728827::CT	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3739008058, ss5206239958	NC_000012.11:49585494::TCTC	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss4251504425, ss5485509947, ss5756003500	NC_000012.12:49191711::TCTC	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
3933913635	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3693637869	NC_000012.12:49191717::TCTC	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3739008059	NC_000012.11:49585494::TCTCTC	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss4251504426, ss5485509945	NC_000012.12:49191711::TCTCTC	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
3933913635	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3693637870	NC_000012.12:49191717::TCTCTC	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss4251504427	NC_000012.12:49191711::TCTCTCTC	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
3933913635	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss4251504428	NC_000012.12:49191711::TCTCTCTCTC	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
3933913635	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
3933913635	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3170447806	NC_000012.12:49191711::TCTCTCTCTCTC	NC_000012.12:49191711:TCTCTCTCTCTC… NC_000012.12:49191711:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT

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

No publications for rs1555163170

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

rs1555163170