Name: rs9299384
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.

rs9299384

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr9:104990326-104990344 (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)₉ / del(T)₇ / del(T)₅ / del(…
del(T)₉ / del(T)₇ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₄ / dup(T)₁₅ / dup(T)₁₆ / dup(T)₁₇ / dup(T)₁₈ / ins(T)₂₉
Variation Type: Indel Insertion and Deletion
Frequency: dup(T)₄=0.0966 (890/9210, ALFA)
delT=0.2063 (1033/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CT70 : 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	9210	TTTTTTTTTTTTTTTTTTT=0.8445	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0009, TTTTTTTTTTTTTTTTTTTTT=0.0441, TTTTTTTTTTTTTTTTTTTTTTT=0.0966, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0012, TTTTTTTTTTTTTTTTTTTTTT=0.0099, TTTTTTTTTTTTTTTTTTTTTTTT=0.0028, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.850746	0.045017	0.104237	32
European	Sub	7996	TTTTTTTTTTTTTTTTTTT=0.8210	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0010, TTTTTTTTTTTTTTTTTTTTT=0.0508, TTTTTTTTTTTTTTTTTTTTTTT=0.1112, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0014, TTTTTTTTTTTTTTTTTTTTTT=0.0114, TTTTTTTTTTTTTTTTTTTTTTTT=0.0033, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.825486	0.052721	0.121793	32
African	Sub	732	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	22	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	710	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	38	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	26	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	12	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	54	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	150	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	54	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	186	TTTTTTTTTTTTTTTTTTT=0.995	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.005, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.989247	0.0	0.010753	0

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	9210	(T)₁₉=0.8445	del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0009, dupTT=0.0441, dupTTT=0.0099, dup(T)₄=0.0966, dup(T)₅=0.0028, dup(T)₆=0.0012, dup(T)₇=0.0000, dup(T)₈=0.0000, dup(T)₉=0.0000, dup(T)₁₀=0.0000, dup(T)₁₅=0.0000
Allele Frequency Aggregator	European	Sub	7996	(T)₁₉=0.8210	del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0010, dupTT=0.0508, dupTTT=0.0114, dup(T)₄=0.1112, dup(T)₅=0.0033, dup(T)₆=0.0014, dup(T)₇=0.0000, dup(T)₈=0.0000, dup(T)₉=0.0000, dup(T)₁₀=0.0000, dup(T)₁₅=0.0000
Allele Frequency Aggregator	African	Sub	732	(T)₁₉=1.000	del(T)₇=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₉=0.000, dup(T)₁₀=0.000, dup(T)₁₅=0.000
Allele Frequency Aggregator	Other	Sub	186	(T)₁₉=0.995	del(T)₇=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.005, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₉=0.000, dup(T)₁₀=0.000, dup(T)₁₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	150	(T)₁₉=1.000	del(T)₇=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₉=0.000, dup(T)₁₀=0.000, dup(T)₁₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	54	(T)₁₉=1.00	del(T)₇=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₀=0.00, dup(T)₁₅=0.00
Allele Frequency Aggregator	South Asian	Sub	54	(T)₁₉=1.00	del(T)₇=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₀=0.00, dup(T)₁₅=0.00
Allele Frequency Aggregator	Asian	Sub	38	(T)₁₉=1.00	del(T)₇=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₀=0.00, dup(T)₁₅=0.00
1000Genomes	Global	Study-wide	5008	(T)₁₉=0.7937	delT=0.2063
1000Genomes	African	Sub	1322	(T)₁₉=0.7133	delT=0.2867
1000Genomes	East Asian	Sub	1008	(T)₁₉=0.7758	delT=0.2242
1000Genomes	Europe	Sub	1006	(T)₁₉=0.8569	delT=0.1431
1000Genomes	South Asian	Sub	978	(T)₁₉=0.796	delT=0.204
1000Genomes	American	Sub	694	(T)₁₉=0.879	delT=0.121

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 9	NC_000009.12:g.104990336_104990344del
GRCh38.p14 chr 9	NC_000009.12:g.104990338_104990344del
GRCh38.p14 chr 9	NC_000009.12:g.104990340_104990344del
GRCh38.p14 chr 9	NC_000009.12:g.104990341_104990344del
GRCh38.p14 chr 9	NC_000009.12:g.104990342_104990344del
GRCh38.p14 chr 9	NC_000009.12:g.104990343_104990344del
GRCh38.p14 chr 9	NC_000009.12:g.104990344del
GRCh38.p14 chr 9	NC_000009.12:g.104990344dup
GRCh38.p14 chr 9	NC_000009.12:g.104990343_104990344dup
GRCh38.p14 chr 9	NC_000009.12:g.104990342_104990344dup
GRCh38.p14 chr 9	NC_000009.12:g.104990341_104990344dup
GRCh38.p14 chr 9	NC_000009.12:g.104990340_104990344dup
GRCh38.p14 chr 9	NC_000009.12:g.104990339_104990344dup
GRCh38.p14 chr 9	NC_000009.12:g.104990338_104990344dup
GRCh38.p14 chr 9	NC_000009.12:g.104990337_104990344dup
GRCh38.p14 chr 9	NC_000009.12:g.104990336_104990344dup
GRCh38.p14 chr 9	NC_000009.12:g.104990335_104990344dup
GRCh38.p14 chr 9	NC_000009.12:g.104990331_104990344dup
GRCh38.p14 chr 9	NC_000009.12:g.104990330_104990344dup
GRCh38.p14 chr 9	NC_000009.12:g.104990329_104990344dup
GRCh38.p14 chr 9	NC_000009.12:g.104990328_104990344dup
GRCh38.p14 chr 9	NC_000009.12:g.104990327_104990344dup
GRCh38.p14 chr 9	NC_000009.12:g.104990344_104990345insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 9	NC_000009.11:g.107752617_107752625del
GRCh37.p13 chr 9	NC_000009.11:g.107752619_107752625del
GRCh37.p13 chr 9	NC_000009.11:g.107752621_107752625del
GRCh37.p13 chr 9	NC_000009.11:g.107752622_107752625del
GRCh37.p13 chr 9	NC_000009.11:g.107752623_107752625del
GRCh37.p13 chr 9	NC_000009.11:g.107752624_107752625del
GRCh37.p13 chr 9	NC_000009.11:g.107752625del
GRCh37.p13 chr 9	NC_000009.11:g.107752625dup
GRCh37.p13 chr 9	NC_000009.11:g.107752624_107752625dup
GRCh37.p13 chr 9	NC_000009.11:g.107752623_107752625dup
GRCh37.p13 chr 9	NC_000009.11:g.107752622_107752625dup
GRCh37.p13 chr 9	NC_000009.11:g.107752621_107752625dup
GRCh37.p13 chr 9	NC_000009.11:g.107752620_107752625dup
GRCh37.p13 chr 9	NC_000009.11:g.107752619_107752625dup
GRCh37.p13 chr 9	NC_000009.11:g.107752618_107752625dup
GRCh37.p13 chr 9	NC_000009.11:g.107752617_107752625dup
GRCh37.p13 chr 9	NC_000009.11:g.107752616_107752625dup
GRCh37.p13 chr 9	NC_000009.11:g.107752612_107752625dup
GRCh37.p13 chr 9	NC_000009.11:g.107752611_107752625dup
GRCh37.p13 chr 9	NC_000009.11:g.107752610_107752625dup
GRCh37.p13 chr 9	NC_000009.11:g.107752609_107752625dup
GRCh37.p13 chr 9	NC_000009.11:g.107752608_107752625dup
GRCh37.p13 chr 9	NC_000009.11:g.107752625_107752626insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: CT70, uncharacterized CT70 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CT70 transcript variant X2	XR_002956864.2:n.	N/A	Intron Variant
CT70 transcript variant X4	XR_007061707.1:n.	N/A	Intron Variant
CT70 transcript variant X5	XR_007061708.1:n.	N/A	Intron Variant
CT70 transcript variant X1	XR_001746866.2:n.	N/A	Genic Downstream Transcript Variant
CT70 transcript variant X3	XR_001746867.2:n.	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	(T)₁₉=	del(T)₉	del(T)₇	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₄	dup(T)₁₅	dup(T)₁₆	dup(T)₁₇	dup(T)₁₈	ins(T)₂₉
GRCh38.p14 chr 9	NC_000009.12:g.104990326_104990344=	NC_000009.12:g.104990336_104990344del	NC_000009.12:g.104990338_104990344del	NC_000009.12:g.104990340_104990344del	NC_000009.12:g.104990341_104990344del	NC_000009.12:g.104990342_104990344del	NC_000009.12:g.104990343_104990344del	NC_000009.12:g.104990344del	NC_000009.12:g.104990344dup	NC_000009.12:g.104990343_104990344dup	NC_000009.12:g.104990342_104990344dup	NC_000009.12:g.104990341_104990344dup	NC_000009.12:g.104990340_104990344dup	NC_000009.12:g.104990339_104990344dup	NC_000009.12:g.104990338_104990344dup	NC_000009.12:g.104990337_104990344dup	NC_000009.12:g.104990336_104990344dup	NC_000009.12:g.104990335_104990344dup	NC_000009.12:g.104990331_104990344dup	NC_000009.12:g.104990330_104990344dup	NC_000009.12:g.104990329_104990344dup	NC_000009.12:g.104990328_104990344dup	NC_000009.12:g.104990327_104990344dup	NC_000009.12:g.104990344_104990345insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 9	NC_000009.11:g.107752607_107752625=	NC_000009.11:g.107752617_107752625del	NC_000009.11:g.107752619_107752625del	NC_000009.11:g.107752621_107752625del	NC_000009.11:g.107752622_107752625del	NC_000009.11:g.107752623_107752625del	NC_000009.11:g.107752624_107752625del	NC_000009.11:g.107752625del	NC_000009.11:g.107752625dup	NC_000009.11:g.107752624_107752625dup	NC_000009.11:g.107752623_107752625dup	NC_000009.11:g.107752622_107752625dup	NC_000009.11:g.107752621_107752625dup	NC_000009.11:g.107752620_107752625dup	NC_000009.11:g.107752619_107752625dup	NC_000009.11:g.107752618_107752625dup	NC_000009.11:g.107752617_107752625dup	NC_000009.11:g.107752616_107752625dup	NC_000009.11:g.107752612_107752625dup	NC_000009.11:g.107752611_107752625dup	NC_000009.11:g.107752610_107752625dup	NC_000009.11:g.107752609_107752625dup	NC_000009.11:g.107752608_107752625dup	NC_000009.11:g.107752625_107752626insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

74 SubSNP, 40 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95523119	Feb 05, 2009 (130)
2	HUMANGENOME_JCVI	ss97764861	Feb 13, 2009 (130)
3	PJP	ss295432571	May 09, 2011 (137)
4	PJP	ss295432572	May 09, 2011 (134)
5	1000GENOMES	ss1368593971	Aug 21, 2014 (142)
6	EVA_UK10K_ALSPAC	ss1706507516	Apr 01, 2015 (144)
7	EVA_UK10K_ALSPAC	ss1706507518	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1706507530	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1706507531	Apr 01, 2015 (144)
10	SWEGEN	ss3005377107	Nov 08, 2017 (151)
11	SWEGEN	ss3005377108	Nov 08, 2017 (151)
12	SWEGEN	ss3005377109	Nov 08, 2017 (151)
13	SWEGEN	ss3005377110	Nov 08, 2017 (151)
14	SWEGEN	ss3005377111	Nov 08, 2017 (151)
15	EVA_DECODE	ss3724490703	Jul 13, 2019 (153)
16	EVA_DECODE	ss3724490704	Jul 13, 2019 (153)
17	EVA_DECODE	ss3724490705	Jul 13, 2019 (153)
18	EVA_DECODE	ss3724490706	Jul 13, 2019 (153)
19	EVA_DECODE	ss3724490707	Jul 13, 2019 (153)
20	EVA_DECODE	ss3724490708	Jul 13, 2019 (153)
21	PACBIO	ss3786487907	Jul 13, 2019 (153)
22	PACBIO	ss3791693028	Jul 13, 2019 (153)
23	PACBIO	ss3796574504	Jul 13, 2019 (153)
24	KHV_HUMAN_GENOMES	ss3812693404	Jul 13, 2019 (153)
25	EVA	ss3831792043	Apr 26, 2020 (154)
26	GNOMAD	ss4207157312	Apr 26, 2021 (155)
27	GNOMAD	ss4207157313	Apr 26, 2021 (155)
28	GNOMAD	ss4207157314	Apr 26, 2021 (155)
29	GNOMAD	ss4207157315	Apr 26, 2021 (155)
30	GNOMAD	ss4207157316	Apr 26, 2021 (155)
31	GNOMAD	ss4207157317	Apr 26, 2021 (155)
32	GNOMAD	ss4207157318	Apr 26, 2021 (155)
33	GNOMAD	ss4207157319	Apr 26, 2021 (155)
34	GNOMAD	ss4207157320	Apr 26, 2021 (155)
35	GNOMAD	ss4207157321	Apr 26, 2021 (155)
36	GNOMAD	ss4207157322	Apr 26, 2021 (155)
37	GNOMAD	ss4207157323	Apr 26, 2021 (155)
38	GNOMAD	ss4207157324	Apr 26, 2021 (155)
39	GNOMAD	ss4207157325	Apr 26, 2021 (155)
40	GNOMAD	ss4207157326	Apr 26, 2021 (155)
41	GNOMAD	ss4207157327	Apr 26, 2021 (155)
42	GNOMAD	ss4207157329	Apr 26, 2021 (155)
43	GNOMAD	ss4207157330	Apr 26, 2021 (155)
44	GNOMAD	ss4207157331	Apr 26, 2021 (155)
45	GNOMAD	ss4207157332	Apr 26, 2021 (155)
46	GNOMAD	ss4207157333	Apr 26, 2021 (155)
47	GNOMAD	ss4207157334	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5194697953	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5194697954	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5194697955	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5194697956	Apr 26, 2021 (155)
52	TOMMO_GENOMICS	ss5194697957	Apr 26, 2021 (155)
53	TOMMO_GENOMICS	ss5194697958	Apr 26, 2021 (155)
54	1000G_HIGH_COVERAGE	ss5281719878	Oct 13, 2022 (156)
55	1000G_HIGH_COVERAGE	ss5281719879	Oct 13, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5281719880	Oct 13, 2022 (156)
57	1000G_HIGH_COVERAGE	ss5281719881	Oct 13, 2022 (156)
58	1000G_HIGH_COVERAGE	ss5281719882	Oct 13, 2022 (156)
59	1000G_HIGH_COVERAGE	ss5281719883	Oct 13, 2022 (156)
60	HUGCELL_USP	ss5477629841	Oct 13, 2022 (156)
61	HUGCELL_USP	ss5477629842	Oct 13, 2022 (156)
62	HUGCELL_USP	ss5477629843	Oct 13, 2022 (156)
63	HUGCELL_USP	ss5477629844	Oct 13, 2022 (156)
64	HUGCELL_USP	ss5477629845	Oct 13, 2022 (156)
65	HUGCELL_USP	ss5477629846	Oct 13, 2022 (156)
66	TOMMO_GENOMICS	ss5739051796	Oct 13, 2022 (156)
67	TOMMO_GENOMICS	ss5739051797	Oct 13, 2022 (156)
68	TOMMO_GENOMICS	ss5739051798	Oct 13, 2022 (156)
69	TOMMO_GENOMICS	ss5739051799	Oct 13, 2022 (156)
70	TOMMO_GENOMICS	ss5739051800	Oct 13, 2022 (156)
71	TOMMO_GENOMICS	ss5739051801	Oct 13, 2022 (156)
72	EVA	ss5829566565	Oct 13, 2022 (156)
73	EVA	ss5829566566	Oct 13, 2022 (156)
74	EVA	ss5829566567	Oct 13, 2022 (156)
75	1000Genomes	NC_000009.11 - 107752607	Oct 12, 2018 (152)
76	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 26234397 (NC_000009.11:107752606::TTTT 787/3854) Row 26234398 (NC_000009.11:107752606::TTT 494/3854)	-	Oct 12, 2018 (152)
77	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 26234397 (NC_000009.11:107752606::TTTT 787/3854) Row 26234398 (NC_000009.11:107752606::TTT 494/3854)	-	Oct 12, 2018 (152)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
99	gnomAD - Genomes Submission ignored due to conflicting rows: Row 333848474 (NC_000009.12:104990325::T 910/109182) Row 333848475 (NC_000009.12:104990325::TT 7442/109096) Row 333848476 (NC_000009.12:104990325::TTT 3133/109170)...	-	Apr 26, 2021 (155)
100	8.3KJPN Submission ignored due to conflicting rows: Row 52667260 (NC_000009.11:107752606::TTTT 3922/16682) Row 52667261 (NC_000009.11:107752606::T 421/16682) Row 52667262 (NC_000009.11:107752606:T: 597/16682)...	-	Apr 26, 2021 (155)
101	8.3KJPN Submission ignored due to conflicting rows: Row 52667260 (NC_000009.11:107752606::TTTT 3922/16682) Row 52667261 (NC_000009.11:107752606::T 421/16682) Row 52667262 (NC_000009.11:107752606:T: 597/16682)...	-	Apr 26, 2021 (155)
102	8.3KJPN Submission ignored due to conflicting rows: Row 52667260 (NC_000009.11:107752606::TTTT 3922/16682) Row 52667261 (NC_000009.11:107752606::T 421/16682) Row 52667262 (NC_000009.11:107752606:T: 597/16682)...	-	Apr 26, 2021 (155)
103	8.3KJPN Submission ignored due to conflicting rows: Row 52667260 (NC_000009.11:107752606::TTTT 3922/16682) Row 52667261 (NC_000009.11:107752606::T 421/16682) Row 52667262 (NC_000009.11:107752606:T: 597/16682)...	-	Apr 26, 2021 (155)
104	8.3KJPN Submission ignored due to conflicting rows: Row 52667260 (NC_000009.11:107752606::TTTT 3922/16682) Row 52667261 (NC_000009.11:107752606::T 421/16682) Row 52667262 (NC_000009.11:107752606:T: 597/16682)...	-	Apr 26, 2021 (155)
105	8.3KJPN Submission ignored due to conflicting rows: Row 52667260 (NC_000009.11:107752606::TTTT 3922/16682) Row 52667261 (NC_000009.11:107752606::T 421/16682) Row 52667262 (NC_000009.11:107752606:T: 597/16682)...	-	Apr 26, 2021 (155)
106	14KJPN Submission ignored due to conflicting rows: Row 72888900 (NC_000009.12:104990325::TTTT 6897/28256) Row 72888901 (NC_000009.12:104990325:T: 1062/28256) Row 72888902 (NC_000009.12:104990325::TTT 239/28256)...	-	Oct 13, 2022 (156)
107	14KJPN Submission ignored due to conflicting rows: Row 72888900 (NC_000009.12:104990325::TTTT 6897/28256) Row 72888901 (NC_000009.12:104990325:T: 1062/28256) Row 72888902 (NC_000009.12:104990325::TTT 239/28256)...	-	Oct 13, 2022 (156)
108	14KJPN Submission ignored due to conflicting rows: Row 72888900 (NC_000009.12:104990325::TTTT 6897/28256) Row 72888901 (NC_000009.12:104990325:T: 1062/28256) Row 72888902 (NC_000009.12:104990325::TTT 239/28256)...	-	Oct 13, 2022 (156)
109	14KJPN Submission ignored due to conflicting rows: Row 72888900 (NC_000009.12:104990325::TTTT 6897/28256) Row 72888901 (NC_000009.12:104990325:T: 1062/28256) Row 72888902 (NC_000009.12:104990325::TTT 239/28256)...	-	Oct 13, 2022 (156)
110	14KJPN Submission ignored due to conflicting rows: Row 72888900 (NC_000009.12:104990325::TTTT 6897/28256) Row 72888901 (NC_000009.12:104990325:T: 1062/28256) Row 72888902 (NC_000009.12:104990325::TTT 239/28256)...	-	Oct 13, 2022 (156)
111	14KJPN Submission ignored due to conflicting rows: Row 72888900 (NC_000009.12:104990325::TTTT 6897/28256) Row 72888901 (NC_000009.12:104990325:T: 1062/28256) Row 72888902 (NC_000009.12:104990325::TTT 239/28256)...	-	Oct 13, 2022 (156)
112	UK 10K study - Twins Submission ignored due to conflicting rows: Row 26234397 (NC_000009.11:107752606::TTTT 785/3708) Row 26234398 (NC_000009.11:107752606::TTT 426/3708)	-	Oct 12, 2018 (152)
113	UK 10K study - Twins Submission ignored due to conflicting rows: Row 26234397 (NC_000009.11:107752606::TTTT 785/3708) Row 26234398 (NC_000009.11:107752606::TTT 426/3708)	-	Oct 12, 2018 (152)
114	ALFA	NC_000009.12 - 104990326	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)
rs150339837	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4207157334	NC_000009.12:104990325:TTTTTTTTT:	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
5048722599	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4207157333	NC_000009.12:104990325:TTTTT:	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
5048722599	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4207157332	NC_000009.12:104990325:TTTT:	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
5048722599	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4207157331	NC_000009.12:104990325:TTT:	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
5048722599	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4207157330	NC_000009.12:104990325:TT:	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
5048722599	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
47228632, ss1368593971, ss5194697955	NC_000009.11:107752606:T:	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3724490703, ss3812693404, ss4207157329, ss5281719883, ss5477629841, ss5739051797	NC_000009.12:104990325:T:	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
5048722599	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3005377111, ss5194697954	NC_000009.11:107752606::T	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4207157312, ss5281719878, ss5477629842, ss5739051799	NC_000009.12:104990325::T	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
5048722599	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3724490704	NC_000009.12:104990326::T	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3005377108, ss3786487907, ss3791693028, ss3796574504, ss5194697958	NC_000009.11:107752606::TT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4207157313, ss5281719882, ss5477629846, ss5739051801	NC_000009.12:104990325::TT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
5048722599	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3724490705	NC_000009.12:104990326::TT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss1706507518, ss1706507531, ss3005377109, ss5194697956, ss5829566567	NC_000009.11:107752606::TTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4207157314, ss5281719881, ss5477629845, ss5739051798	NC_000009.12:104990325::TTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
5048722599	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3724490706	NC_000009.12:104990326::TTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss295432571	NC_000009.10:106792428::TTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1706507516, ss1706507530, ss3005377107, ss3831792043, ss5194697953, ss5829566565	NC_000009.11:107752606::TTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4207157315, ss5281719880, ss5477629843, ss5739051796	NC_000009.12:104990325::TTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
5048722599	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3724490707	NC_000009.12:104990326::TTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss97764861	NT_008470.19:36917138::TTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95523119	NT_008470.19:36917157::TTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss295432572	NC_000009.10:106792442::TTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3005377110, ss5194697957, ss5829566566	NC_000009.11:107752606::TTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4207157316, ss5281719879, ss5477629844, ss5739051800	NC_000009.12:104990325::TTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
5048722599	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3724490708	NC_000009.12:104990326::TTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4207157317	NC_000009.12:104990325::TTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5048722599	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4207157318	NC_000009.12:104990325::TTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5048722599	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4207157319	NC_000009.12:104990325::TTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5048722599	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4207157320	NC_000009.12:104990325::TTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5048722599	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4207157321	NC_000009.12:104990325::TTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5048722599	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4207157322	NC_000009.12:104990325::TTTTTTTTTT… NC_000009.12:104990325::TTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4207157323	NC_000009.12:104990325::TTTTTTTTTT… NC_000009.12:104990325::TTTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5048722599	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4207157324	NC_000009.12:104990325::TTTTTTTTTT… NC_000009.12:104990325::TTTTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4207157325	NC_000009.12:104990325::TTTTTTTTTT… NC_000009.12:104990325::TTTTTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4207157326	NC_000009.12:104990325::TTTTTTTTTT… NC_000009.12:104990325::TTTTTTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4207157327	NC_000009.12:104990325::TTTTTTTTTT… NC_000009.12:104990325::TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3597172489	NC_000009.12:104990325:TTTTTTT:	NC_000009.12:104990325:TTTTTTTTTTT… NC_000009.12:104990325:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT

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

No publications for rs9299384

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

rs9299384