Variant #0000509245 (NC_000002.11:g.132236920C>G, NM_001085365.1:c.*4714G>C (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.132236920C>G
DNA change (hg38) g.131479347C>G
Published as TUBA3D(NM_080386.3):c.266C>G (p.(Pro89Arg))
ISCN -
DB-ID MZT2A_000001
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 2019-07-18 18:22:55 +02:00 (CEST)
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     
MZT2A NM_001085365.1 ?/. - c.*4714G>C r.(=) p.(=)
TUBA3D NM_080386.3 ?/. - c.266C>G r.(?) p.(Pro89Arg)


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