Variant #0000803798 (NC_000009.11:g.103340711G>C, NM_001018116.1:c.286G>C (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.103340711G>C
DNA change (hg38) -
Published as CAVIN4(NM_001018116.2):c.286G>C (p.V96L)
ISCN -
DB-ID MSANTD3_000001
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MURC NM_001018116.1 ?/. - c.286G>C r.(?) p.(Val96Leu)
MSANTD3-TMEFF1 NM_001198812.1 ?/. - c.*1829G>C r.(=) p.(=)
TMEFF1 NM_003692.4 ?/. - c.*1829G>C r.(=) p.(=)
MSANTD3 NM_080655.2 ?/. - c.*127463G>C r.(=) p.(=)


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