Variant #0000273750 (NC_000014.8:g.31358935G>C, NM_004086.2:c.1591G>C (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.31358935G>C
DNA change (hg38) g.30889729G>C
Published as COCH(NM_001135058.1):c.1591G>C (p.E531Q)
ISCN -
DB-ID COCH_000010 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +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.-136130G>C r.(?) p.(=)
COCH NM_004086.2 ?/. - c.1591G>C r.(?) p.(Glu531Gln)
STRN3 NM_014574.3 ?/. - c.*5682C>G r.(=) p.(=)


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