Variant #0001056250 (NC_000017.10:g.80765511_80765516del, NM_005993.4:c.1115_1120del (TBCD))

Chromosome 17
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.80765511_80765516del
DNA change (hg38) -
Published as TBCD(NM_005993.5):c.1115_1120del (p.(Lys372_Asp373del))
ISCN -
DB-ID TBCD_000061
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 2025-11-01 13:22:20 +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     
TBCD NM_005993.4 ?/. - c.1115_1120del r.(?) p.(Lys372_Asp373del)
ZNF750 NM_024702.2 ?/. - c.*22509_*22514del r.(=) p.(=)


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