Variant #0000571307 (NC_000022.10:g.19171098C>T, NM_005984.3:c.-4912G>A (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.19171098C>T
DNA change (hg38) g.19183585C>T
Published as CLTCL1(NM_007098.3):c.4632G>A (p.S1544=)
ISCN -
DB-ID CLTCL1_000009
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) 7.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-17 10:32:09 +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.-4912G>A r.(?) p.(=)
CLTCL1 NM_007098.3 -?/. - c.4632G>A r.(?) p.(Ser1544=)


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