Variant #0000552495 (NC_000014.8:g.31355057C>T, NM_004086.2:c.1016C>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.31355057C>T
DNA change (hg38) g.30885851C>T
Published as COCH(NM_001135058.1):c.1016C>T (p.T339I)
ISCN -
DB-ID COCH_000022
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COCH NM_004086.2 ?/. - c.1016C>T r.(?) p.(Thr339Ile)
STRN3 NM_014574.3 ?/. - c.*9560G>A r.(=) p.(=)


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