Variant #0000994956 (NC_000005.9:g.179227937G>C, NM_014275.4:c.575C>G (MGAT4B))

Chromosome 5
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.179227937G>C
DNA change (hg38) -
Published as MGAT4B(NM_014275.4):c.575C>G (p.(Thr192Ser))
ISCN -
DB-ID LTC4S_000004
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MGAT4B NM_014275.4 ?/. - c.575C>G r.(?) p.(Thr192Ser)
LTC4S NM_145867.1 ?/. - c.*4542G>C r.(=) p.(=)


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