Variant #0000504113 (NC_000001.10:g.168262526_168262527insTT, NC_000001.10(NM_005149.2):c.603+10_603+11insTT (TBX19))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.168262526_168262527insTT
DNA change (hg38) g.168293288_168293289insTT
Published as TBX19(NM_005149.2):c.603+9_603+10insTT
ISCN -
DB-ID TBX19_000010
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
TBX19 NM_005149.2 -/. - c.603+10_603+11insTT r.(=) p.(=)


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