Variant #0000921778 (NC_000014.8:g.31355191C>T, NM_004086.2:c.1150C>T (COCH))

Chromosome 14
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.31355191C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID COCH_000063
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs756541797
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 9.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-03-21 15:31:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COCH NM_004086.2 ?/. - c.1150C>T r.(?) p.(Arg384Cys)


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