Variant #0000610260 (NC_000006.11:g.3154414A>G, NM_001069.2:c.1021T>C (TUBB2A))

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.3154414A>G
DNA change (hg38) g.3154180A>G
Published as TUBB2A(NM_001069.2):c.1021T>C (p.(Phe341Leu))
ISCN -
DB-ID BPHL_000002
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TUBB2A NM_001069.2 ?/. - c.1021T>C r.(?) p.(Phe341Leu)
BPHL NM_004332.2 ?/. - c.*1605A>G r.(=) p.(=)


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