Variant #0000524430 (NC_000005.9:g.139227913C>A, NM_013982.2:c.2166G>T (NRG2))

Chromosome 5
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.139227913C>A
DNA change (hg38) g.139848328C>A
Published as NRG2(NM_013982.2):c.2166G>T (p.E722D)
ISCN -
DB-ID NRG2_000006
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NRG2 NM_013982.2 ?/. - c.2166G>T r.(?) p.(Glu722Asp)
PSD2 NM_032289.2 ?/. - c.*5854C>A r.(=) p.(=)


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