Variant #0000623133 (NC_000014.8:g.31346836T>C, NM_004086.2:c.141T>C (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.31346836T>C
DNA change (hg38) g.30877630T>C
Published as COCH(NM_001347720.1):c.336T>C (p.D112=)
ISCN -
DB-ID COCH_000024 See all 2 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) 9.0E-5 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-07-05 13:57:26 +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.141T>C r.(?) p.(Asp47=)
STRN3 NM_014574.3 -?/. - c.*17781A>G r.(=) p.(=)


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