Variant #0000976957 (NC_000006.11:g.127796839C>T, NM_014702.4:c.-16640G>A (KIAA0408))

Chromosome 6
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.127796839C>T
DNA change (hg38) -
Published as SOGA3(NM_001395923.1):c.2332G>A (p.G778S)
ISCN -
DB-ID KIAA0408_000002
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SOGA3 NM_001012279.2 ?/. - c.2332G>A r.(?) p.(Gly778Ser)
KIAA0408 NM_014702.4 ?/. - c.-16640G>A r.(?) p.(=)


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