Variant #0000340467 (NC_000011.9:g.792579G>A, NM_001191060.1:c.561C>T (SLC25A22))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.792579G>A
DNA change (hg38) g.792579G>A
Published as -
ISCN -
DB-ID SLC25A22_000011
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) 0.00916 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-29 12:53:52 +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.561C>T r.(?) p.(Tyr187=)
CEND1 NM_016564.3 -/. - c.-2632C>T r.(?) p.(=)
PIDD NM_145886.3 -/. - c.*6728C>T r.(=) p.(=)


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