Variant #0000805854 (NC_000012.11:g.56494932T>C, NM_001982.3:c.3289T>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.56494932T>C
DNA change (hg38) -
Published as ERBB3(NM_001982.3):c.3289T>C (p.(Ser1097Pro), p.S1097P)
ISCN -
DB-ID ERBB3_000017 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) 0.00064 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERBB3 NM_001982.3 ?/. - c.3289T>C r.(?) p.(Ser1097Pro)
PA2G4 NM_006191.2 ?/. - c.-3590T>C r.(?) p.(=)


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