Variant #0000309691 (NC_000019.9:g.54697134G>A, NM_024298.3:c.-3949C>T (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.54697134G>A
DNA change (hg38) g.54193279G>A
Published as TSEN34(NM_001282332.2):c.850G>A (p.V284I)
ISCN -
DB-ID TSEN34_000003
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) 8.0E-5 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     
TSEN34 NM_024075.3 ?/. - c.850G>A r.(?) p.(Val284Ile)
MBOAT7 NM_024298.3 ?/. - c.-3949C>T r.(?) p.(=)


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