Variant #0000950972 (NC_000017.10:g.59489879_59489885del, NM_005994.3:c.*4012_*4018del (TBX2))

Chromosome 17
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.59489879_59489885del
DNA change (hg38) -
Published as C17orf82(NM_203425.1):c.543_549del (p.(Pro182Asnfs*29))
ISCN -
DB-ID C17orf82_000003
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 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     
TBX2 NM_005994.3 -?/. - c.*4012_*4018del r.(=) p.(=)
C17orf82 NM_203425.1 -?/. - c.543_549del r.(?) p.(Pro182Asnfs*29)


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