Variant #0000532293 (NC_000007.13:g.56131957_56131958insCC, NM_006213.4:c.*16790_*16791insGG (PHKG1))

Chromosome 7
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.56131957_56131958insCC
DNA change (hg38) g.56064264_56064265insCC
Published as SUMF2(NM_015411.3):c.-49_-48insCC
ISCN -
DB-ID CCT6A_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) Retrieve
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 2020-06-22 17:29:29 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCT6A NM_001762.3 ?/. - c.*1179_*1180insCC r.(=) p.(=)
PHKG1 NM_006213.4 ?/. - c.*16790_*16791insGG r.(=) p.(=)
SUMF2 NM_015411.2 ?/. - c.10_11insCC r.(?) p.(His4ProfsTer17)


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