Variant #0000680949 (NC_000017.10:g.59560588C>A, NM_018488.2:c.1349C>A (TBX4))

Chromosome 17
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.59560588C>A
DNA change (hg38) -
Published as TBX4(NM_001321120.2):c.1352C>A (p.T451N), TBX4(NM_018488.3):c.1349C>A (p.T450N)
ISCN -
DB-ID TBX4_000039 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) 1.0E-5 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBX4 NM_018488.2 ?/. - c.1349C>A r.(?) p.(Thr450Asn)


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