Variant #0000253879 (NC_000014.8:g.31359024A>T, NM_004086.2:c.*27A>T (COCH))

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.31359024A>T
DNA change (hg38) g.30889818A>T
Published as COCH(NM_001135058.1):c.*27A>T
ISCN -
DB-ID COCH_000011
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) 0.24855 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AP4S1 NM_001128126.2 -/. - c.-136041A>T r.(?) p.(=)
COCH NM_004086.2 -/. - c.*27A>T r.(=) p.(=)
STRN3 NM_014574.3 -/. - c.*5593T>A r.(=) p.(=)


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