Variant #0000528906 (NC_000006.11:g.43017858T>C, NM_014780.4:c.1412A>G (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.43017858T>C
DNA change (hg38) g.43050120T>C
Published as CUL7(NM_001168370.1):c.1664A>G (p.(Tyr555Cys))
ISCN -
DB-ID CUL7_000029
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) 0.00014 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CUL7 NM_014780.4 ?/. - c.1412A>G r.(?) p.(Tyr471Cys)
MRPL2 NM_015950.3 ?/. - c.*4154A>G r.(=) p.(=)
KLC4 NM_138343.2 ?/. - c.-9591T>C r.(?) p.(=)


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