Variant #0000865118 (NC_000017.10:g.26696021C>G, NM_080669.4:c.*30651G>C (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.26696021C>G
DNA change (hg38) -
Published as VTN(NM_000638.3):c.698G>C (p.(Gly233Ala))
ISCN -
DB-ID SEBOX_000005
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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VTN NM_000638.3 ?/. - c.698G>C r.(?) p.(Gly233Ala)
SEBOX NM_001080837.2 ?/. - c.-3770G>C r.(?) p.(=)
SLC46A1 NM_080669.4 ?/. - c.*30651G>C r.(=) p.(=)


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