Variant #0000657437 (NC_000014.8:g.31349926C>T, NM_004086.2:c.615C>T (COCH))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.31349926C>T
DNA change (hg38) g.30880720C>T
Published as COCH(NM_001347720.1):c.810C>T (p.G270=)
ISCN -
DB-ID COCH_000049
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) 0.0005 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-07-05 13:58:37 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COCH NM_004086.2 -?/. - c.615C>T r.(?) p.(Gly205=)
STRN3 NM_014574.3 -?/. - c.*14691G>A r.(=) p.(=)


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