Variant #0000717835 (NC_000002.11:g.130914172C>A, NM_017951.4:c.1291G>T (SMPD4))

Chromosome 2
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.130914172C>A
DNA change (hg38) -
Published as SMPD4(NM_017951.5):c.1174G>T (p.A392S)
ISCN -
DB-ID MZT2B_000017
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) 3.0E-5 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMPD4 NM_017951.4 ?/. - c.1291G>T r.(?) p.(Ala431Ser)
MZT2B NM_025029.3 ?/. - c.-25684C>A r.(?) p.(=)


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