Variant #0000983577 (NC_000019.9:g.49129204C>G, NC_000019.9(NM_001204158.2):c.40-121C>G (SPHK2))

Chromosome 19
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.49129204C>G
DNA change (hg38) -
Published as SPHK2(NM_020126.5):c.96C>G (p.(Val32=))
ISCN -
DB-ID DBP_000003
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) 2.0E-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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL18 NM_000979.3 ?/. - c.-6804G>C r.(?) p.(=)
SPHK2 NM_001204158.2 ?/. - c.40-121C>G r.(=) p.(=)
DBP NM_001352.3 ?/. - c.*4890G>C r.(=) p.(=)


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