Variant #0000654586 (NC_000002.11:g.230673034C>T, NM_001284214.1:c.2273G>A (TRIP12))

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.230673034C>T
DNA change (hg38) g.229808318C>T
Published as TRIP12(NM_001284214.1):c.2273G>A (p.(Cys758Tyr)), TRIP12(NM_001348325.2):c.2273G>A (p.C758Y)
ISCN -
DB-ID TRIP12_000059 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIP12 NM_001284214.1 -?/. - c.2273G>A r.(?) p.(Cys758Tyr)


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