Variant #0000613519 (NC_000011.9:g.6412984G>A, NM_000543.4:c.689G>A (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.6412984G>A
DNA change (hg38) g.6391754G>A
Published as SMPD1(NM_000543.5):c.689G>A (p.(Arg230His)), SMPD1(NM_001318087.2):c.689G>A (p.R230H)
ISCN -
DB-ID SMPD1_000066 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) 0.0002 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMPD1 NM_000543.4 ?/. - c.689G>A r.(?) p.(Arg230His)
APBB1 NM_001164.2 ?/. - c.*3780C>T r.(=) p.(=)


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