Variant #0000298422 (NC_000011.9:g.6415463G>A, NM_000543.4:c.1522G>A (SMPD1))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.6415463G>A
DNA change (hg38) g.6394233G>A
Published as SMPD1(NM_000543.5):c.1522G>A (p.G508R), SMPD1(NM_001318088.2):c.601G>A (p.G201R)
ISCN -
DB-ID SMPD1_000101 See all 37 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) 0.19173 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMPD1 NM_000543.4 -/. - c.1522G>A r.(?) p.(Gly508Arg)
APBB1 NM_001164.2 -/. - c.*1301C>T r.(=) p.(=)


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