Variant #0000355095 (NC_000011.9:g.1861912G>A, NC_000011.9(NM_003282.3):c.186+26G>A (TNNI2))

Chromosome 11
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.1861912G>A
DNA change (hg38) g.1840682G>A
Published as -
ISCN -
DB-ID TNNI2_000006
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2271441
Origin Germline
Segregation -
Frequency 0.06-0.22
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.18308 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2009-08-28 18:20:46 +02:00 (CEST)
Date last edited 2012-11-02 20:43:05 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNNI2 NM_003282.3 ?/. 5i c.186+26G>A r.(?) p.(=)


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