Variant #0000979915 (NC_000011.9:g.792589G>C, NM_001191060.1:c.551C>G (SLC25A22))

Chromosome 11
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.792589G>C
DNA change (hg38) -
Published as SLC25A22(NM_001191061.2):c.551C>G (p.(Ala184Gly))
ISCN -
DB-ID CEND1_000012
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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC25A22 NM_001191060.1 ?/. - c.551C>G r.(?) p.(Ala184Gly)
CEND1 NM_016564.3 ?/. - c.-2642C>G r.(?) p.(=)
PIDD NM_145886.3 ?/. - c.*6718C>G r.(=) p.(=)


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