Variant #0000690685 (NC_000010.10:g.135106137G>A, NM_001256617.1:c.1164C>T (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.135106137G>A
DNA change (hg38) -
Published as TUBGCP2(NM_001256617.1):c.1164C>T (p.H388=)
ISCN -
DB-ID TUBGCP2_000010
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) 0.0028 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +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     
TUBGCP2 NM_001256617.1 -?/. - c.1164C>T r.(?) p.(His388=)
ZNF511 NM_145806.2 -?/. - c.-16311G>A r.(?) p.(=)


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