Variant #0000273749 (NC_000014.8:g.31346846C>T, NM_004086.2:c.151C>T (COCH))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.31346846C>T
DNA change (hg38) g.30877640C>T
Published as COCH(NM_001135058.1):c.151C>T (p.P51S), COCH(NM_001135058.2):c.151C>T (p.P51S)
ISCN -
DB-ID COCH_000004 See all 5 reported entries
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 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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COCH NM_004086.2 +/. - c.151C>T r.(?) p.(Pro51Ser)
STRN3 NM_014574.3 +/. - c.*17771G>A r.(=) p.(=)


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