Variant #0000291581 (NC_000019.9:g.54687439_54687440del, NM_024298.3:c.458_459del (MBOAT7))

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.54687439_54687440del
DNA change (hg38) g.54183556_54183557del
Published as MBOAT7(NM_024298.4):c.458_459delTC (p.L153Qfs*142)
ISCN -
DB-ID MBOAT7_000001 See all 2 reported entries
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-16 13:32:53 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MBOAT7 NM_024298.3 ?/. - c.458_459del r.(?) p.(Leu153GlnfsTer142)


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