Variant #0000562827 (NC_000017.10:g.6387600C>T, NM_031220.3:c.287G>A (PITPNM3))

Chromosome 17
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.6387600C>T
DNA change (hg38) g.6484280C>T
Published as PITPNM3(NM_031220.3):c.287G>A (p.R96Q), PITPNM3(NM_031220.4):c.287G>A (p.R96Q)
ISCN -
DB-ID PITPNM3_000030 See all 2 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) 0.00038 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 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PITPNM3 NM_031220.3 ?/. - c.287G>A r.(?) p.(Arg96Gln)


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