Variant #0000848948 (NC_000002.11:g.132236937G>A, NM_001085365.1:c.*4697C>T (MZT2A))

Chromosome 2
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.132236937G>A
DNA change (hg38) -
Published as TUBA3D(NM_080386.3):c.283G>A (p.G95R)
ISCN -
DB-ID MZT2A_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) 0 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MZT2A NM_001085365.1 ?/. - c.*4697C>T r.(=) p.(=)
TUBA3D NM_080386.3 ?/. - c.283G>A r.(?) p.(Gly95Arg)


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