Variant #0000302185 (NC_000011.9:g.792590C>T, NM_001191060.1:c.550G>A (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.792590C>T
DNA change (hg38) g.792590C>T
Published as SLC25A22(NM_001191060.1):c.550G>A (p.A184T)
ISCN -
DB-ID SLC25A22_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) 0 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC25A22 NM_001191060.1 ?/. - c.550G>A r.(?) p.(Ala184Thr)
CEND1 NM_016564.3 ?/. - c.-2643G>A r.(?) p.(=)
PIDD NM_145886.3 ?/. - c.*6717G>A r.(=) p.(=)


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