Variant #0000849738 (NC_000002.11:g.220115512T>C, NM_001008910.2:c.*2231T>C (STK16))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.220115512T>C
DNA change (hg38) -
Published as TUBA4A(NM_001278552.2):c.864A>G (p.V288=), TUBA4A(NM_006000.3):c.909A>G (p.V303=)
ISCN -
DB-ID TUBA4A_000001 See all 3 reported entries
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) 0.00451 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STK16 NM_001008910.2 -/. - c.*2231T>C r.(=) p.(=)
TUBA4A NM_006000.1 -/. - c.909A>G r.(?) p.(Val303=)


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