Variant #0000126772 (NC_000011.9:g.22214903G>C, NM_213599.2:c.-136G>C (ANO5))

Chromosome 11
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.22214903G>C
DNA change (hg38) g.22193357G>C
Published as -
ISCN -
DB-ID ANO5_000026 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs12792259
Origin Germline
Segregation -
Frequency -
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 2010-02-14 22:37:07 +01:00 (CET)
Date last edited 2012-11-02 20:40:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANO5 NM_213599.2 ?/. 1 c.-136G>C r.(?) p.(=)


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