Variant #0000532294 (NC_000007.13:g.56136277C>T, NM_006213.4:c.*12470G>A (PHKG1))

Chromosome 7
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.56136277C>T
DNA change (hg38) g.56068584C>T
Published as SUMF2(NM_015411.3):c.170C>T (p.A57V)
ISCN -
DB-ID CCT6A_000004
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) 0.00021 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCT6A NM_001762.3 -?/. - c.*5499C>T r.(=) p.(=)
PHKG1 NM_006213.4 -?/. - c.*12470G>A r.(=) p.(=)
SUMF2 NM_015411.2 -?/. - c.227C>T r.(?) p.(Ala76Val)


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