Variant #0000328143 (NC_000002.11:g.230701593C>T, NM_001284214.1:c.1241G>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.230701593C>T
DNA change (hg38) g.229836877C>T
Published as TRIP12(NM_001284214.1):c.1241G>A (p.(Arg414Gln)), TRIP12(NM_004238.3):c.1115G>A (p.R372Q)
ISCN -
DB-ID TRIP12_000010 See all 2 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIP12 NM_001284214.1 -?/. - c.1241G>A r.(?) p.(Arg414Gln)


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