Variant #0000308302 (NC_000022.10:g.19164209G>A, NC_000022.10(NM_005984.3):c.632-3C>T (SLC25A1))

Chromosome 22
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.19164209G>A
DNA change (hg38) g.19176696G>A
Published as SLC25A1(NM_005984.4):c.632-3C>T
ISCN -
DB-ID SLC25A1_000023
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) 0.00014 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-17 10:29:36 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC25A1 NM_005984.3 -?/. - c.632-3C>T r.spl? p.?
CLTCL1 NM_007098.3 -?/. - c.*3294C>T r.(=) p.(=)


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