Variant #0000657817 (NC_000016.9:g.30100083C>G, NM_004608.3:c.699G>C (TBX6))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.30100083C>G
DNA change (hg38) g.30088762C>G
Published as TBX6(NM_004608.3):c.699G>C (p.(Trp233Cys))
ISCN -
DB-ID PPP4C_000006 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) 0.00065 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2025-07-08 13:22:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPP4C NM_002720.1 +/. - c.*3700C>G r.(=) p.(=)
TBX6 NM_004608.3 +/. - c.699G>C r.(?) p.(Trp233Cys)
YPEL3 NM_031477.4 +/. - c.*3948G>C r.(=) p.(=)


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