Variant #0000525910 (NC_000005.9:g.6632843G>C, NM_017755.5:c.123C>G (NSUN2))

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.6632843G>C
DNA change (hg38) g.6632730G>C
Published as NSUN2(NM_017755.6):c.123C>G (p.(Ile41Met))
ISCN -
DB-ID NSUN2_000017 See all 2 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) 1.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SRD5A1 NM_001047.2 ?/. - c.-847G>C r.(?) p.(=)
NSUN2 NM_017755.5 ?/. - c.123C>G r.(?) p.(Ile41Met)


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