Variant #0000557912 (NC_000016.9:g.30762640C>T, NC_000016.9(NM_000294.2):c.271+38C>T (PHKG2))

Chromosome 16
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.30762640C>T
DNA change (hg38) g.30751319C>T
Published as -
ISCN -
DB-ID C16orf93_000007
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) 0.9918 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHKG2 NM_000294.2 -/. - c.271+38C>T r.(=) p.(=)
C16orf93 NM_001014979.2 -/. - c.*6157G>A r.(=) p.(=)


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