Variant #0000274642 (NC_000006.11:g.43021548G>A, NM_014780.4:c.-197C>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.43021548G>A
DNA change (hg38) g.43053810G>A
Published as CUL7(NM_001168370.1):c.49C>T (p.H17Y)
ISCN -
DB-ID CUL7_000008
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_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 2020-03-23 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.-197C>T r.(?) p.(=)
MRPL2 NM_015950.3 -?/. - c.*464C>T r.(=) p.(=)
KLC4 NM_138343.2 -?/. - c.-5901G>A r.(?) p.(=)


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