Variant #0000567577 (NC_000019.9:g.4358128G>A, NC_000019.9(NM_032868.4):c.1236+546G>A (MPND))

Chromosome 19
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.4358128G>A
DNA change (hg38) g.4358131G>A
Published as MPND(NM_001300862.1):c.1285G>A (p.V429I)
ISCN -
DB-ID MPND_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) 5.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SH3GL1 NM_003025.3 ?/. - c.*3469C>T r.(=) p.(=)
MPND NM_032868.4 ?/. - c.1236+546G>A r.(=) p.(=)


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