Variant #0000658299 (NC_000017.10:g.79865722C>T, NM_002861.3:c.419G>A (PCYT2))

Chromosome 17
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.79865722C>T
DNA change (hg38) g.81907846C>T
Published as -
ISCN -
DB-ID NPB_000002
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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCYT2 NM_002861.3 ?/. - c.419G>A r.(?) p.(Arg140His)
SIRT7 NM_016538.2 ?/. - c.*4570G>A r.(=) p.(=)
NPB NM_148896.3 ?/. - c.*5098C>T r.(=) p.(=)


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