Variant #0000968884 (NC_000017.10:g.40762123C>A, NC_000017.10(NM_001070.4):c.50-3C>A (TUBG1))

Chromosome 17
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.40762123C>A
DNA change (hg38) -
Published as TUBG1(NM_001070.4):c.50-3C>A, TUBG1(NM_001070.5):c.50-3C>A
ISCN -
DB-ID FAM134C_000011 See all 3 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) 1.0E-5 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 2024-02-26 20:06:56 +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.50-3C>A r.spl? p.?
FAM134C NM_178126.3 -?/. - c.-781G>T r.(?) p.(=)


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