Variant #0000571304 (NC_000022.10:g.19165823C>G, NC_000022.10(NM_005984.3):c.95-70G>C (SLC25A1))

Chromosome 22
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.19165823C>G
DNA change (hg38) g.19178310C>G
Published as SLC25A1(NM_001256534.1):c.46G>C (p.G16R)
ISCN -
DB-ID CLTCL1_000006
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) 0.00377 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 2024-04-19 20:27:30 +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.95-70G>C r.(=) p.(=)
CLTCL1 NM_007098.3 -/. - c.*1680G>C r.(=) p.(=)


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