Variant #0000304545 (NC_000008.10:g.32621386G>A, NM_013956.3:c.1404G>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.32621386G>A
DNA change (hg38) g.32763868G>A
Published as NRG1(NM_013956.4):c.1404G>A (p.M468I)
ISCN -
DB-ID NRG1_000022
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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NRG1 NM_013956.3 ?/. - c.1404G>A r.(?) p.(Met468Ile)
NRG1 NM_013964.3 ?/. - c.1389G>A r.(?) p.(Met463Ile)


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