Variant #0001043698 (NC_000022.10:g.19164101G>T, NM_005984.3:c.737C>A (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.19164101G>T
DNA change (hg38) -
Published as SLC25A1(NM_005984.5):c.737C>A (p.(Thr246Asn))
ISCN -
DB-ID CLTCL1_000019
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC25A1 NM_005984.3 ?/. - c.737C>A r.(?) p.(Thr246Asn)
CLTCL1 NM_007098.3 ?/. - c.*3402C>A r.(=) p.(=)


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