Variant #0000248892 (NC_000012.11:g.56494998A>T, NM_001982.3:c.3355A>T (ERBB3))

Chromosome 12
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.56494998A>T
DNA change (hg38) g.56101214A>T
Published as ERBB3(NM_001982.4):c.3355A>T (p.S1119C)
ISCN -
DB-ID ERBB3_000019
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) 0.08925 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 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     
ERBB3 NM_001982.3 -/. - c.3355A>T r.(?) p.(Ser1119Cys)
PA2G4 NM_006191.2 -/. - c.-3524A>T r.(?) p.(=)


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