Variant #0000554306 (NC_000015.9:g.43689494C>T, NM_014444.2:c.1254C>T (TUBGCP4))

Chromosome 15
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.43689494C>T
DNA change (hg38) g.43397296C>T
Published as TUBGCP4(NM_001286414.2):c.1254C>T (p.I418=), TUBGCP4(NM_014444.5):c.1254C>T (p.(Ile418=))
ISCN -
DB-ID TUBGCP4_000006 See all 2 reported entries
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) 0.00336 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TUBGCP4 NM_014444.2 -?/. - c.1254C>T r.(?) p.(Ile418=)


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