Variant #0000321825 (NC_000010.10:g.135113012C>T, NM_001256617.1:c.375G>A (TUBGCP2))

Chromosome 10
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.135113012C>T
DNA change (hg38) g.133299508C>T
Published as TUBGCP2(NM_001256617.1):c.375G>A (p.(=))
ISCN -
DB-ID TUBGCP2_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) 1.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-29 11:34:03 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TUBGCP2 NM_001256617.1 ?/. - c.375G>A r.(?) p.(Ala125=)
ZNF511 NM_145806.2 ?/. - c.-9436C>T r.(?) p.(=)


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