Variant #0000298419 (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) g.6390736_6390741del
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_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 2021-09-17 14:40:49 +02:00 (CEST)
Options




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.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.