Variant #0000887147 (NC_000006.11:g.3154537T>C, NM_001069.2:c.898A>G (TUBB2A))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.3154537T>C
DNA change (hg38) -
Published as TUBB2A(NM_001069.3):c.898A>G (p.M300V)
ISCN -
DB-ID BPHL_000007
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +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     
TUBB2A NM_001069.2 +?/. - c.898A>G r.(?) p.(Met300Val)
BPHL NM_004332.2 +?/. - c.*1728T>C r.(=) p.(=)


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