Variant #0000607806 (NC_000002.11:g.230656754_230656756dup, NM_001284214.1:c.4160_4162dup (TRIP12))

Chromosome 2
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.230656754_230656756dup
DNA change (hg38) g.229792038_229792040dup
Published as TRIP12(NM_004238.1):c.4018_4019insATG (p.(Asn1339_Val1340insAsp))
ISCN -
DB-ID TRIP12_000054
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 2019-12-04 14:54:23 +01:00 (CET)
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     
TRIP12 NM_001284214.1 ?/. - c.4160_4162dup r.(?) p.(Asn1387_Val1388insAsp)


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