Variant #0001050361 (NC_000001.10:g.179852117G>A, NC_000001.10(NM_001267578.1):c.475+5G>A (TOR1AIP1))

Chromosome 1
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.179852117G>A
DNA change (hg38) -
Published as TOR1AIP1(NM_015602.4):c.475+5G>A
ISCN -
DB-ID TOR1AIP2_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) 8.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TOR1AIP1 NM_001267578.1 ?/. - c.475+5G>A r.spl? p.?
TOR1AIP1 NM_015602.3 ?/. - c.475+5G>A r.spl? p.?
TOR1AIP2 NM_145034.4 ?/. - c.-5571C>T r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.