Variant #0001055524 (NC_000016.9:g.30100436C>T, NM_004608.3:c.449G>A (TBX6))

Chromosome 16
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.30100436C>T
DNA change (hg38) -
Published as TBX6(NM_004608.4):c.449G>A (p.(Arg150His))
ISCN -
DB-ID PPP4C_000028
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPP4C NM_002720.1 ?/. - c.*4053C>T r.(=) p.(=)
TBX6 NM_004608.3 ?/. - c.449G>A r.(?) p.(Arg150His)
YPEL3 NM_031477.4 ?/. - c.*3595G>A r.(=) p.(=)


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