Variant #0000314442 (NC_000022.10:g.19748690G>A, NM_080647.1:c.297G>A (TBX1))

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.19748690G>A
DNA change (hg38) g.19761167G>A
Published as TBX1(NM_001379200.1):c.324G>A (p.(Ala108=)), TBX1(NM_080647.1):c.297G>A (p.A99=)
ISCN -
DB-ID TBX1_000002 See all 4 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) 0.02332 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 2018-01-15 20:58:59 +01:00 (CET)
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     
TBX1 NM_080647.1 -/. - c.297G>A r.(?) p.(Ala99=)


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