Variant #0000316654 (NC_000019.9:g.54672410C>T, NM_024298.3:c.*5328G>A (MBOAT7))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.54672410C>T
DNA change (hg38) g.54168684C>T
Published as TMC4(NM_001145303.2):c.460-4G>A
ISCN -
DB-ID TMC4_000001
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) 0.0054 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-16 13:30:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMC4 NM_001145303.1 -/. - c.461-4G>A r.spl? p.?
MBOAT7 NM_024298.3 -/. - c.*5328G>A r.(=) p.(=)


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