Variant #0000266869 (NC_000014.8:g.31355096C>G, NM_004086.2:c.1055C>G (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.31355096C>G
DNA change (hg38) g.30885890C>G
Published as COCH(NM_001135058.1):c.1055C>G (p.T352S), COCH(NM_001135058.2):c.1055C>G (p.T352S), LOC100506071(NR_038356.1):n.975G>C
ISCN -
DB-ID COCH_000007 See all 3 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) 0.55894 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.1055C>G r.(?) p.(Thr352Ser)
STRN3 NM_014574.3 -/. - c.*9521G>C r.(=) p.(=)


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