Variant #0000808343 (NC_000017.10:g.79862793C>T, NM_002861.3:c.1086G>A (PCYT2))

Chromosome 17
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.79862793C>T
DNA change (hg38) -
Published as PCYT2(NM_001330518.1):c.1020G>A (p.K340=)
ISCN -
DB-ID ALYREF_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) 0.00016 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCYT2 NM_002861.3 -?/. - c.1086G>A r.(?) p.(Lys362=)
ALYREF NM_005782.3 -?/. - c.-13337G>A r.(?) p.(=)
ANAPC11 NM_016476.10 -?/. - c.*4852C>T r.(=) p.(=)
NPB NM_148896.3 -?/. - c.*2169C>T r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.