Variant #0000321994 (NC_000011.9:g.6411935T>C, NM_000543.4:c.107T>C (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.6411935T>C
DNA change (hg38) g.6390705T>C
Published as SMPD1(NM_000543.4):c.107T>C (p.V36A, p.(Val36Ala)), SMPD1(NM_000543.4):c.107_113delTGCTGGCinsCGCTGGC (p.V36A), SMPD1(NM_000543.5):c.103_108delCTGGT...
ISCN -
DB-ID SMPD1_000115 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) 0.55418 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.107T>C r.(?) p.(Val36Ala)
APBB1 NM_001164.2 ?/. - c.*4829A>G r.(=) p.(=)


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