Variant #0001035792 (NC_000006.11:g.43019001C>A, NM_014780.4:c.938G>T (CUL7))

Chromosome 6
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.43019001C>A
DNA change (hg38) -
Published as CUL7(NM_014780.5):c.938G>T (p.(Trp313Leu))
ISCN -
DB-ID CUL7_000113
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 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CUL7 NM_014780.4 ?/. - c.938G>T r.(?) p.(Trp313Leu)
MRPL2 NM_015950.3 ?/. - c.*3011G>T r.(=) p.(=)
KLC4 NM_138343.2 ?/. - c.-8448C>A r.(?) p.(=)


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