Variant #0000321262 (NC_000001.10:g.204506603T>G, NM_002393.4:c.389T>G (MDM4))

Chromosome 1
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.204506603T>G
DNA change (hg38) g.204537475T>G
Published as MDM4(NM_002393.4):c.389T>G (p.(Ile130Ser))
ISCN -
DB-ID MDM4_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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MDM4 NM_002393.4 ?/. - c.389T>G r.(?) p.(Ile130Ser)
LRRN2 NM_006338.2 ?/. - c.*80376A>C r.(=) p.(=)


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