Variant #0000304648 (NC_000005.9:g.6632744G>A, NM_017755.5:c.222C>T (NSUN2))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.6632744G>A
DNA change (hg38) g.6632631G>A
Published as NSUN2(NM_017755.5):c.222C>T (p.L74=)
ISCN -
DB-ID NSUN2_000008
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) 0.00195 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-16 17:40:01 +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.-946G>A r.(?) p.(=)
NSUN2 NM_017755.5 -?/. - c.222C>T r.(?) p.(Leu74=)


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