Variant #0001004964 (NC_000019.9:g.49120006C>T, NM_001204158.2:c.-2908C>T (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.49120006C>T
DNA change (hg38) -
Published as RPL18(NM_000979.3):c.274G>A (p.(Val92Ile))
ISCN -
DB-ID FAM83E_000004
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
RPL18 NM_000979.3 -?/. - c.274G>A r.(?) p.(Val92Ile)
SPHK2 NM_001204158.2 -?/. - c.-2908C>T r.(?) p.(=)
FAM83E NM_017708.3 -?/. - c.-3377G>A r.(?) p.(=)
SPACA4 NM_133498.2 -?/. - c.*9396C>T r.(=) p.(=)


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