Variant #0000727553 (NC_000019.9:g.6368554G>A, NM_006012.2:c.667G>A (CLPP))

Chromosome 19
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.6368554G>A
DNA change (hg38) -
Published as CLPP(NM_006012.2):c.667G>A (p.A223T)
ISCN -
DB-ID ALKBH7_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) 7.0E-5 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLPP NM_006012.2 ?/. - c.667G>A r.(?) p.(Ala223Thr)
ALKBH7 NM_032306.3 ?/. - c.-4278G>A r.(?) p.(=)


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