Variant #0000888469 (NC_000008.10:g.90983460G>A, NM_002485.4:c.643C>T (NBN))

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.90983460G>A
DNA change (hg38) -
Published as NBN(NM_001024688.2):c.397C>T (p.R133W), NBN(NM_002485.4):c.643C>T (p.R215W, p.(Arg215Trp)), NBN(NM_002485.5):c.643C>T (p.R215W)
ISCN -
DB-ID NBN_000020 See all 8 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) 0.00247 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NBN NM_002485.4 ?/. - c.643C>T r.(?) p.(Arg215Trp)


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