Variant #0000544870 (NC_000011.9:g.6412931T>C, NM_000543.4:c.636T>C (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.6412931T>C
DNA change (hg38) g.6391701T>C
Published as SMPD1(NM_000543.5):c.636T>C (p.D212=), SMPD1(NM_001318087.2):c.636T>C (p.D212=)
ISCN -
DB-ID SMPD1_000123 See all 3 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) 0.1236 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.636T>C r.(?) p.(Asp212=)
APBB1 NM_001164.2 -/. - c.*3833A>G r.(=) p.(=)


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