Variant #0000322350 (NC_000011.9:g.67406397del, NC_000011.9(NM_005995.4):c.7+546del (TBX10))

Chromosome 11
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.67406397del
DNA change (hg38) g.67638926del
Published as TBX10(NM_005995.4):c.7+546del (p.(=))
ISCN -
DB-ID TBX10_000001
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 2018-01-15 20:58:59 +01:00 (CET)
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     
TBX10 NM_005995.4 ?/. - c.7+546del r.(=) p.(=)
ACY3 NM_080658.1 ?/. - c.*3804del r.(?) p.(=)


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