Variant #0000286710 (NC_000009.11:g.103340658C>T, NM_001018116.1:c.233C>T (MURC))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.103340658C>T
DNA change (hg38) g.100578376C>T
Published as CAVIN4(NM_001018116.2):c.233C>T (p.S78L)
ISCN -
DB-ID MURC_000002
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) 0.00157 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MURC NM_001018116.1 -/. - c.233C>T r.(?) p.(Ser78Leu)
MSANTD3-TMEFF1 NM_001198812.1 -/. - c.*1776C>T r.(=) p.(=)
TMEFF1 NM_003692.4 -/. - c.*1776C>T r.(=) p.(=)
MSANTD3 NM_080655.2 -/. - c.*127410C>T r.(=) p.(=)


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