Variant #0000994687 (NC_000005.9:g.139227776C>T, NM_013982.2:c.2303G>A (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.139227776C>T
DNA change (hg38) -
Published as NRG2(NM_004883.2):c.2279G>A (p.(Arg760Lys))
ISCN -
DB-ID NRG2_000012
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) 0.00325 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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.2303G>A r.(?) p.(Arg768Lys)
PSD2 NM_032289.2 ?/. - c.*5717C>T r.(=) p.(=)


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