Variant #0000655954 (NC_000008.10:g.104413815G>A, NM_030780.3:c.741C>T (SLC25A32))

Chromosome 8
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.104413815G>A
DNA change (hg38) g.103401587G>A
Published as SLC25A32(NM_030780.4):c.741C>T (p.V247=)
ISCN -
DB-ID DCAF13_000001
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DCAF13 NM_015420.6 -?/. - c.-13404G>A r.(?) p.(=)
SLC25A32 NM_030780.3 -?/. - c.741C>T r.(?) p.(Val247=)


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