Variant #0000617735 (NC_000019.9:g.49120041G>A, NM_001204158.2:c.-2873G>A (SPHK2))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.49120041G>A
DNA change (hg38) g.48616784G>A
Published as RPL18(NM_000979.3):c.239C>T (p.(Ala80Val))
ISCN -
DB-ID FAM83E_000001
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) 0.00043 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL18 NM_000979.3 -?/. - c.239C>T r.(?) p.(Ala80Val)
SPHK2 NM_001204158.2 -?/. - c.-2873G>A r.(?) p.(=)
FAM83E NM_017708.3 -?/. - c.-3412C>T r.(?) p.(=)
SPACA4 NM_133498.2 -?/. - c.*9431G>A r.(=) p.(=)


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