Variant #0000514702 (NC_000002.11:g.220115274C>T, NM_001008910.2:c.*1993C>T (STK16))

Chromosome 2
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.220115274C>T
DNA change (hg38) g.219250552C>T
Published as TUBA4A(NM_001278552.1):c.1102G>A (p.(Ala368Thr))
ISCN -
DB-ID STK16_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) 1.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STK16 NM_001008910.2 +/. - c.*1993C>T r.(=) p.(=)
TUBA4A NM_006000.1 +/. - c.1147G>A r.(?) p.(Ala383Thr)


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