Variant #0000930711 (NC_000017.10:g.26696867G>A, NM_080669.4:c.*29805C>T (SLC46A1))

Chromosome 17
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.26696867G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID SEBOX_000006
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) 1.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VTN NM_000638.3 ?/. - c.190C>T r.(?) p.(Arg64Cys)
SEBOX NM_001080837.2 ?/. - c.-4616C>T r.(?) p.(=)
SLC46A1 NM_080669.4 ?/. - c.*29805C>T r.(=) p.(=)


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