Variant #0000324058 (NC_000015.9:g.43658424T>G, NM_014444.2:c.-5129T>G (TUBGCP4))

Chromosome 15
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.43658424T>G
DNA change (hg38) g.43366226T>G
Published as ZSCAN29(NM_152455.3):c.1106A>C (p.(His369Pro))
ISCN -
DB-ID ZSCAN29_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) 2.0E-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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TUBGCP4 NM_014444.2 ?/. - c.-5129T>G r.(?) p.(=)
ZSCAN29 NM_152455.3 ?/. - c.1106A>C r.(?) p.(His369Pro)


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