Variant #0001055522 (NC_000016.9:g.30099872_30099873del, NM_004608.3:c.833_834del (TBX6))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.30099872_30099873del
DNA change (hg38) -
Published as TBX6(NM_004608.4):c.833_834del (p.(Cys278*))
ISCN -
DB-ID PPP4C_000026
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPP4C NM_002720.1 +?/. - c.*3489_*3490del r.(=) p.(=)
TBX6 NM_004608.3 +?/. - c.833_834del r.(?) p.(Cys278*)
YPEL3 NM_031477.4 +?/. - c.*4159_*4160del r.(=) p.(=)


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