Variant #0000313586 (NC_000006.11:g.3154344_3154346del, NM_001069.2:c.1090_1092del (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.3154344_3154346del
DNA change (hg38) g.3154110_3154112del
Published as TUBB2A(NM_001069.3):c.1090_1092delTCG (p.S364del)
ISCN -
DB-ID TUBB2A_000005
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.1090_1092del r.(?) p.(Ser364del)
BPHL NM_004332.2 +?/. - c.*1535_*1537del r.(=) p.(=)


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