Variant #0000544873 (NC_000011.9:g.6413108T>C, NM_000543.4:c.813T>C (SMPD1))

Chromosome 11
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.6413108T>C
DNA change (hg38) g.6391878T>C
Published as SMPD1(NM_000543.4):c.813T>C (p.P271=), SMPD1(NM_000543.5):c.813T>C (p.P271=)
ISCN -
DB-ID SMPD1_000153 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) 0.0043 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMPD1 NM_000543.4 -?/. - c.813T>C r.(?) p.(Pro271=)
APBB1 NM_001164.2 -?/. - c.*3656A>G r.(=) p.(=)


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