Variant #0000568383 (NC_000019.9:g.54682480A>C, NC_000019.9(NM_024298.3):c.1031+2T>G (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.54682480A>C
DNA change (hg38) g.54178763A>C
Published as MBOAT7(NM_001146082.2):c.1033T>G (p.*345Gext*8)
ISCN -
DB-ID MBOAT7_000006
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-16 13:31:05 +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.1031+2T>G r.spl? p.?


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