Variant #0000893575 (NC_000017.10:g.40765072C>T, NM_001070.4:c.587C>T (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.40765072C>T
DNA change (hg38) -
Published as TUBG1(NM_001070.5):c.587C>T (p.T196M)
ISCN -
DB-ID FAM134C_000012
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 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TUBG1 NM_001070.4 ?/. - c.587C>T r.(?) p.(Thr196Met)
FAM134C NM_178126.3 ?/. - c.-3730G>A r.(?) p.(=)


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