Variant #0000443194 (NC_000012.11:g.56088477C>T, NM_002206.2:c.2199G>A (ITGA7))

Chromosome 12
Allele Unknown
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.56088477C>T
DNA change (hg38) g.55694693C>T
Published as -
ISCN -
DB-ID ITGA7_000014
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs75740263
Origin Germline
Segregation -
Frequency 0.06-0.07
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2010-11-14 15:42:16 +01:00 (CET)
Date last edited 2012-11-02 20:42:42 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ITGA7 NM_002206.2 ?/. 16 c.2199G>A r.(?) p.(=)


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