Variant #0000913643 (NC_000011.9:g.6411966_6411971del, NM_000543.4:c.138_143del (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.6411966_6411971del
DNA change (hg38) -
Published as SMPD1(NM_000543.4):c.138_143delGCTGGC (p.A48_L49del), SMPD1(NM_000543.5):c.138_143delGCTGGC (p.A48_L49del), SMPD1(NM_001318087.1):c.138_143delGCTGG...
ISCN -
DB-ID SMPD1_000119 See all 4 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMPD1 NM_000543.4 -/. - c.138_143del r.(?) p.(Ala48_Leu49del)
APBB1 NM_001164.2 -/. - c.*4823_*4828del r.(=) p.(=)


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