Variant #0000979707 (NC_000011.9:g.6411966_6411971dup, NM_000543.4:c.138_143dup (SMPD1))

Chromosome 11
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.6411966_6411971dup
DNA change (hg38) -
Published as SMPD1(NM_000543.5):c.138_143dup (p.(Ala48_Leu49dup))
ISCN -
DB-ID SMPD1_000176
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_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 2024-08-28 13:16:32 +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.138_143dup r.(?) p.(Ala48_Leu49dup)
APBB1 NM_001164.2 ?/. - c.*4823_*4828dup r.(=) p.(=)


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