Variant #0000306352 (NC_000006.11:g.41754598C>T, NM_001134493.1:c.-838C>T (TOMM6))

Chromosome 6
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.41754598C>T
DNA change (hg38) g.41786860C>T
Published as PRICKLE4(NM_013397.5):c.886C>T (p.L296=)
ISCN -
DB-ID PRICKLE4_000003
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-19 11:52:09 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TOMM6 NM_001134493.1 -?/. - c.-838C>T r.(?) p.(=)
PRICKLE4 NM_013397.5 -?/. - c.886C>T r.(?) p.(Leu296=)
USP49 NM_018561.3 -?/. - c.*11817G>A r.(=) p.(=)


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