Variant #0000723744 (NC_000011.9:g.792735C>G, NC_000011.9(NM_001191060.1):c.413-8G>C (SLC25A22))

Chromosome 11
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.792735C>G
DNA change (hg38) -
Published as SLC25A22(NM_001191060.1):c.413-8G>C
ISCN -
DB-ID CEND1_000010
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) 0.00059 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC25A22 NM_001191060.1 -?/. - c.413-8G>C r.(=) p.(=)
CEND1 NM_016564.3 -?/. - c.-2788G>C r.(?) p.(=)
PIDD NM_145886.3 -?/. - c.*6572G>C r.(=) p.(=)


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