Variant #0000931246 (NC_000022.10:g.19753957C>T, NM_080647.1:c.1055C>T (TBX1))

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.19753957C>T
DNA change (hg38) -
Published as TBX1(NM_001379200.1):c.1082C>T (p.(Pro361Leu)), TBX1(NM_080647.1):c.1055C>T (p.P352L)
ISCN -
DB-ID TBX1_000094 See all 2 reported entries
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) 0.0001 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBX1 NM_001379200.1 -?/. - c.1082C>T r.(?) p.(Pro361Leu)
TBX1 NM_080647.1 -?/. - c.1055C>T r.(?) p.(Pro352Leu)


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