Variant #0000974286 (NC_000002.11:g.132238115C>T, NM_001085365.1:c.*3519G>A (MZT2A))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.132238115C>T
DNA change (hg38) -
Published as TUBA3D(NM_080386.4):c.849C>T (p.(His283=))
ISCN -
DB-ID MZT2A_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) 0.00257 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:20:39 +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.*3519G>A r.(=) p.(=)
TUBA3D NM_080386.3 -?/. - c.849C>T r.(?) p.(=)


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