Variant #0000327232 (NC_000002.11:g.130949511C>T, NM_017951.4:c.-10337G>A (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.130949511C>T
DNA change (hg38) g.130191938C>T
Published as TUBA3E(NM_207312.2):c.1246G>A (p.(Gly416Arg))
ISCN -
DB-ID MZT2B_000003
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) 0.00296 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 2024-04-19 20:20:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMPD4 NM_017951.4 ?/. - c.-10337G>A r.(?) p.(=)
MZT2B NM_025029.3 ?/. - c.*1312C>T r.(=) p.(=)
TUBA3E NM_207312.2 ?/. - c.1246G>A r.(?) p.(Gly416Arg)


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