Variant #0000509180 (NC_000002.11:g.130931095G>A, NM_017951.4:c.378C>T (SMPD4))

Chromosome 2
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.130931095G>A
DNA change (hg38) g.130173522G>A
Published as SMPD4(NM_017951.4):c.378C>T (p.L126=)
ISCN -
DB-ID MZT2B_000007
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) 0.00372 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMPD4 NM_017951.4 -/. - c.378C>T r.(?) p.(Leu126=)
MZT2B NM_025029.3 -/. - c.-8761G>A r.(?) p.(=)


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