Variant #0000621550 (NC_000005.9:g.179223263G>A, NM_014275.4:c.*1782C>T (MGAT4B))

Chromosome 5
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.179223263G>A
DNA change (hg38) g.179796262G>A
Published as LTC4S(NM_145867.1):c.321G>A (p.P107=)
ISCN -
DB-ID LTC4S_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) 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-06-18 11:18:37 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MGAT4B NM_014275.4 -?/. - c.*1782C>T r.(=) p.(=)
LTC4S NM_145867.1 -?/. - c.321G>A r.(?) p.(Pro107=)


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