Variant #0000557846 (NC_000016.9:g.30102391G>A, NC_000016.9(NM_004608.3):c.118+6C>T (TBX6))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.30102391G>A
DNA change (hg38) g.30091070G>A
Published as TBX6(NM_004608.3):c.118+6C>T (p.(=))
ISCN -
DB-ID TBX6_000009
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) 0.02267 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBX6 NM_004608.3 -?/. - c.118+6C>T r.(=) p.(=)
YPEL3 NM_031477.4 -?/. - c.*1640C>T r.(=) p.(=)


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