Variant #0000308646 (NC_000011.9:g.6412786G>T, NM_000543.4:c.491G>T (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.6412786G>T
DNA change (hg38) g.6391556G>T
Published as SMPD1(NM_000543.4):c.491G>T (p.G164V)
ISCN -
DB-ID SMPD1_000122
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.491G>T r.(?) p.(Gly164Val)
APBB1 NM_001164.2 ?/. - c.*3978C>A r.(=) p.(=)


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