Variant #0001039358 (NC_000012.11:g.56493441T>C, NM_001982.3:c.2849T>C (ERBB3))

Chromosome 12
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.56493441T>C
DNA change (hg38) -
Published as ERBB3(NM_001982.4):c.2849T>C (p.(Ile950Thr))
ISCN -
DB-ID PA2G4_000008
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) 6.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERBB3 NM_001982.3 ?/. - c.2849T>C r.(?) p.(Ile950Thr)
PA2G4 NM_006191.2 ?/. - c.-5081T>C r.(?) p.(=)


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