Variant #0000305691 (NC_000017.10:g.6428686G>A, NM_031220.3:c.216C>T (PITPNM3))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.6428686G>A
DNA change (hg38) g.6525366G>A
Published as PITPNM3(NM_031220.3):c.216C>T (p.D72=), PITPNM3(NM_031220.4):c.216C>T (p.D72=)
ISCN -
DB-ID PITPNM3_000017 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) 0.00103 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 2018-01-15 20:58:59 +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     
PITPNM3 NM_031220.3 -?/. - c.216C>T r.(?) p.(Asp72=)


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