Variant #0000681668 (NC_000020.10:g.57605482T>C, NM_030773.3:c.*5644T>C (TUBB1))

Chromosome 20
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.57605482T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID ATP5E_000004
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP5E NM_006886.3 +/. - c.35A>G r.(?) p.(Tyr12Cys)
SLMO2 NM_016045.2 +/. - c.*4580A>G r.(=) p.(=)
TUBB1 NM_030773.3 +/. - c.*5644T>C r.(=) p.(=)


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