Variant #0000296638 (NC_000005.9:g.6632875G>A, NC_000005.9(NM_017755.5):c.97-6C>T (NSUN2))

Chromosome 5
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.6632875G>A
DNA change (hg38) g.6632762G>A
Published as NSUN2(NM_017755.6):c.97-6C>T
ISCN -
DB-ID NSUN2_000009
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) 0.32615 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SRD5A1 NM_001047.2 -/. - c.-815G>A r.(?) p.(=)
NSUN2 NM_017755.5 -/. - c.97-6C>T r.(=) p.(=)


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