Variant #0000296327 (NC_000008.10:g.90995019C>T, NBN(NM_002485.4):c.102G>A)

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.90995019C>T
DNA change (hg38) g.89982791C>T
Published as NBN(NM_002485.4):c.102G>A (p.L34=), NBN(NM_002485.5):c.102G>A (p.L34=)
ISCN -
DB-ID NBN_000052 See all 12 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) 0.35362 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NBN NM_002485.4 -/. - c.102G>A r.(?) p.(Leu34=)