Variant #0000557830 (NC_000016.9:g.30002636C>G, NM_016151.3:c.*3335C>G (TAOK2))

Chromosome 16
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.30002636C>G
DNA change (hg38) g.29991315C>G
Published as TAOK2(NM_004783.3):c.2897C>G (p.A966G)
ISCN -
DB-ID DOC2A_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) 0.00019 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 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     
DOC2A NM_003586.2 ?/. - c.*14871G>C r.(=) p.(=)
HIRIP3 NM_003609.4 ?/. - c.*1892G>C r.(=) p.(=)
TAOK2 NM_016151.3 ?/. - c.*3335C>G r.(=) p.(=)
INO80E NM_173618.1 ?/. - c.-4996C>G r.(?) p.(=)


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