Variant #0000568387 (NC_000019.9:g.54696013G>T, NM_024298.3:c.-2828C>A (MBOAT7))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.54696013G>T
DNA change (hg38) g.54192162G>T
Published as TSEN34(NM_001282332.1):c.534G>T (p.L178F)
ISCN -
DB-ID MBOAT7_000010
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 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     
TSEN34 NM_024075.3 -?/. - c.534G>T r.(?) p.(Leu178Phe)
MBOAT7 NM_024298.3 -?/. - c.-2828C>A r.(?) p.(=)


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