Variant #0000978129 (NC_000008.10:g.145584041G>T, NM_024531.4:c.889G>T (SLC52A2))

Chromosome 8
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.145584041G>T
DNA change (hg38) -
Published as SLC52A2(NM_001363118.1):c.889G>T (p.V297L), SLC52A2(NM_001363118.2):c.889G>T (p.(Val297Leu))
ISCN -
DB-ID SLC52A2_000039 See all 2 reported entries
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) 5.0E-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 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     
SLC52A2 NM_024531.4 ?/. - c.889G>T r.(?) p.(Val297Leu)
FBXL6 NM_024555.5 ?/. - c.-1934C>A r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.