Variant #0000690345 (NC_000009.11:g.103348380_103348400del, NM_001018116.1:c.742_762del (MURC))

Chromosome 9
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.103348380_103348400del
DNA change (hg38) -
Published as CAVIN4(NM_001018116.2):c.742_762delCTGAGACAGTCAGGGGAGAGG (p.L248_R254del)
ISCN -
DB-ID MURC_000003
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-09-15 15:50:26 +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     
MURC NM_001018116.1 ?/. - c.742_762del r.(?) p.(Leu248_Arg254del)


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