Variant #0000690129 (NC_000008.10:g.104419956T>C, NM_030780.3:c.211A>G (SLC25A32))

Chromosome 8
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.104419956T>C
DNA change (hg38) -
Published as SLC25A32(NM_030780.4):c.211A>G (p.T71A)
ISCN -
DB-ID DCAF13_000002
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) 6.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DCAF13 NM_015420.6 ?/. - c.-7263T>C r.(?) p.(=)
SLC25A32 NM_030780.3 ?/. - c.211A>G r.(?) p.(Thr71Ala)


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