Variant #0000262258 (NC_000019.9:g.6372980G>A, NM_006012.2:c.*4259G>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.6372980G>A
DNA change (hg38) g.6372969G>A
Published as ALKBH7(NM_032306.4):c.149G>A (p.R50Q)
ISCN -
DB-ID ALKBH7_000001
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 2018-01-15 20:58:59 +01:00 (CET)
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     
PSPN NM_004158.2 ?/. - c.*2325C>T r.(=) p.(=)
CLPP NM_006012.2 ?/. - c.*4259G>A r.(=) p.(=)
ALKBH7 NM_032306.3 ?/. - c.149G>A r.(?) p.(Arg50Gln)


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