Variant #0000950636 (NC_000016.9:g.30100399G>A, NM_004608.3:c.486C>T (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.30100399G>A
DNA change (hg38) -
Published as TBX6(NM_004608.3):c.486C>T (p.G162=)
ISCN -
DB-ID PPP4C_000020
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) 3.0E-5 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 2023-11-27 17:35:39 +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.*4016G>A r.(=) p.(=)
TBX6 NM_004608.3 ?/. - c.486C>T r.(?) p.(=)
YPEL3 NM_031477.4 ?/. - c.*3632C>T r.(=) p.(=)


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