Variant #0000978972 (NC_000010.10:g.135093287C>T, NM_001256617.1:c.2776G>A (TUBGCP2))

Chromosome 10
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.135093287C>T
DNA change (hg38) -
Published as TUBGCP2(NM_006659.4):c.2692G>A (p.(Ala898Thr))
ISCN -
DB-ID ADAM8_000004
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) 0.00111 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 2024-04-19 20:27:30 +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     
ADAM8 NM_001109.4 -?/. - c.-2966G>A r.(?) p.(=)
TUBGCP2 NM_001256617.1 -?/. - c.2776G>A r.(?) p.(Ala926Thr)
ZNF511 NM_145806.2 -?/. - c.-29161C>T r.(?) p.(=)


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