Variant #0000528905 (NC_000006.11:g.43017190C>T, NM_014780.4:c.1780G>A (CUL7))

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.43017190C>T
DNA change (hg38) g.43049452C>T
Published as CUL7(NM_001168370.1):c.2032G>A (p.(Ala678Thr))
ISCN -
DB-ID CUL7_000028
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) 0.00637 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CUL7 NM_014780.4 -?/. - c.1780G>A r.(?) p.(Ala594Thr)
MRPL2 NM_015950.3 -?/. - c.*4822G>A r.(=) p.(=)
KLC4 NM_138343.2 -?/. - c.-10259C>T r.(?) p.(=)


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