Variant #0000300436 (NC_000008.10:g.32621630C>T, NM_013956.3:c.1648C>T (NRG1))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.32621630C>T
DNA change (hg38) g.32764112C>T
Published as NRG1(NM_013956.4):c.1648C>T (p.R550W), NRG1(NM_013956.5):c.1648C>T (p.R550W)
ISCN -
DB-ID NRG1_000024 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) 0.01413 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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.1648C>T r.(?) p.(Arg550Trp)
NRG1 NM_013964.3 -?/. - c.1633C>T r.(?) p.(Arg545Trp)


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