Variant #0001046159 (NC_000008.10:g.32505475C>A, NC_000008.10(NM_013956.3):c.502+31072C>A (NRG1))

Chromosome 8
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.32505475C>A
DNA change (hg38) -
Published as NRG1(NM_001322205.2):c.239C>A (p.P80H)
ISCN -
DB-ID NRG1_000034
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-07-08 13:22:38 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NRG1 NM_013956.3 ?/. - c.502+31072C>A r.(=) p.(=)
NRG1 NM_013964.3 ?/. - c.502+31072C>A r.(=) p.(=)


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