Variant #0000924515 (NC_000006.11:g.43023701C>A, NM_014780.4:c.-2350G>T (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.43023701C>A
DNA change (hg38) -
Published as MRPL2(NM_001300848.1):c.565G>T (p.(Val189Leu))
ISCN -
DB-ID CUL7_000091
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CUL7 NM_014780.4 -?/. - c.-2350G>T r.(?) p.(=)
MRPL2 NM_015950.3 -?/. - c.565G>T r.(?) p.(Val189Leu)
KLC4 NM_138343.2 -?/. - c.-3748C>A r.(?) p.(=)


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