Variant #0000982906 (NC_000017.10:g.79863283T>C, NM_002861.3:c.944A>G (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.79863283T>C
DNA change (hg38) -
Published as PCYT2(NM_002861.5):c.944A>G (p.(Asp315Gly))
ISCN -
DB-ID ALYREF_000003
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) 0.00016 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCYT2 NM_002861.3 ?/. - c.944A>G r.(?) p.(Asp315Gly)
ALYREF NM_005782.3 ?/. - c.-13827A>G r.(?) p.(=)
ANAPC11 NM_016476.10 ?/. - c.*5342T>C r.(=) p.(=)
NPB NM_148896.3 ?/. - c.*2659T>C r.(=) p.(=)


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