Variant #0000562519 (NC_000017.10:g.59560704G>A, NM_018488.2:c.1465G>A (TBX4))

Chromosome 17
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.59560704G>A
DNA change (hg38) g.61483343G>A
Published as TBX4(NM_001321120.2):c.1468G>A (p.A490T), TBX4(NM_018488.2):c.1465G>A (p.(Ala489Thr))
ISCN -
DB-ID TBX4_000030 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) 2.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBX4 NM_018488.2 -?/. - c.1465G>A r.(?) p.(Ala489Thr)


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