Variant #0000914821 (NC_000017.10:g.40767031A>G, NM_001070.4:c.1328A>G (TUBG1))

Chromosome 17
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.40767031A>G
DNA change (hg38) -
Published as TUBG1(NM_001070.4):c.1328A>G (p.Y443C)
ISCN -
DB-ID FAM134C_000014
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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TUBG1 NM_001070.4 ?/. - c.1328A>G r.(?) p.(Tyr443Cys)
FAM134C NM_178126.3 ?/. - c.-5689T>C r.(?) p.(=)


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