Variant #0000561536 (NC_000017.10:g.40766624G>A, NM_001070.4:c.1107G>A (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.40766624G>A
DNA change (hg38) g.42614606G>A
Published as TUBG1(NM_001070.4):c.1107G>A (p.S369=)
ISCN -
DB-ID FAM134C_000006
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) 0.00024 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 2020-07-13 14:03:22 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TUBG1 NM_001070.4 ?/. - c.1107G>A r.(?) p.(Ser369=)
FAM134C NM_178126.3 ?/. - c.-5282C>T r.(?) p.(=)


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