Variant #0001039714 (NC_000013.10:g.45150032G>A, NM_006022.3:c.-139268C>T (TSC22D1))

Chromosome 13
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.45150032G>A
DNA change (hg38) -
Published as TSC22D1(NM_183422.4):c.179C>T (p.(Pro60Leu))
ISCN -
DB-ID TSC22D1_000010
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) 0.00019 View details
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     
TSC22D1 NM_006022.3 ?/. - c.-139268C>T r.(?) p.(=)
TSC22D1-AS1 NR_038381.1 ?/. - n.1G>A r.(?) -


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