Variant #0000860032 (NC_000005.9:g.908588A>G, NC_000005.9(NM_004237.3):c.866+12A>G (TRIP13))

Chromosome 5
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.908588A>G
DNA change (hg38) -
Published as TRIP13(NM_004237.4):c.866+12A>G
ISCN -
DB-ID BRD9_000004
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) 0.0367 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIP13 NM_004237.3 -/. - c.866+12A>G r.(=) p.(=)
BRD9 NM_023924.4 -/. - c.-15816T>C r.(?) p.(=)


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