Variant #0001043703 (NC_000022.10:g.19168297_19168298del, NM_005984.3:c.-2109_-2108del (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.19168297_19168298del
DNA change (hg38) -
Published as CLTCL1(NM_007098.4):c.4852_4853del (p.(Leu1619Alafs*16))
ISCN -
DB-ID CLTCL1_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_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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC25A1 NM_005984.3 ?/. - c.-2109_-2108del r.(?) p.(=)
CLTCL1 NM_007098.3 ?/. - c.4852_4853del r.(?) p.(Leu1619Alafs*16)


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