Variant #0000976592 (NC_000005.9:g.139227867_139227868insA, NM_013982.2:c.2211_2212insT (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.139227867_139227868insA
DNA change (hg38) -
Published as NRG2(NM_004883.3):c.2187_2188insT (p.(Arg730SerfsTer166))
ISCN -
DB-ID NRG2_000010
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NRG2 NM_013982.2 ?/. - c.2211_2212insT r.(?) p.(Arg738Serfs*166)
PSD2 NM_032289.2 ?/. - c.*5808_*5809insA r.(=) p.(=)


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