Variant #0000279861 (NC_000015.9:g.75188506C>T, NM_002435.1:c.684C>T (MPI))

Chromosome 15
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.75188506C>T
DNA change (hg38) g.74896165C>T
Published as MPI(NM_002435.3):c.684C>T (p.N228=)
ISCN -
DB-ID MPI_000019
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) 0.02581 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MPI NM_002435.1 -/. - c.684C>T r.(?) p.(Asn228=)
FAM219B NM_020447.3 -/. - c.*6454G>A r.(=) p.(=)


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