Variant #0001003880 (NC_000017.10:g.80788710C>T, NC_000017.10(NM_005993.4):c.1318+15900C>T (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.80788710C>T
DNA change (hg38) -
Published as ZNF750(NM_024702.2):c.1480G>A (p.(Ala494Thr))
ISCN -
DB-ID TBCD_000054
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 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 2024-08-28 13:16:32 +02:00 (CEST)
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.1318+15900C>T r.(=) p.(=)
ZNF750 NM_024702.2 ?/. - c.1480G>A r.(?) p.(Ala494Thr)


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