Variant #0001075702 (NC_000006.11:g.3225580G>A, NM_178012.4:c.743C>T (TUBB2B))

Chromosome 6
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.3225580G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID TUBB2B_000031 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs777598117
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-04-29 11:10:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TUBB2B NM_178012.4 ?/. - c.743C>T r.(?) p.(Ala248Val)


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