Variant #0000308301 (NC_000022.10:g.19164702C>A, NM_005984.3:c.457G>T (SLC25A1))

Chromosome 22
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.19164702C>A
DNA change (hg38) g.19177189C>A
Published as SLC25A1(NM_005984.4):c.457G>T (p.D153Y)
ISCN -
DB-ID SLC25A1_000024
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 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     
SLC25A1 NM_005984.3 ?/. - c.457G>T r.(?) p.(Asp153Tyr)
CLTCL1 NM_007098.3 ?/. - c.*2801G>T r.(=) p.(=)


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