Variant #0000557847 (NC_000016.9:g.30129758C>T, NM_024307.2:c.-4959G>A (GDPD3))

Chromosome 16
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.30129758C>T
DNA change (hg38) g.30118437C>T
Published as MAPK3(NM_002746.2):c.455G>A (p.R152Q)
ISCN -
DB-ID GDPD3_000001
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) Retrieve
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 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAPK3 NM_001040056.1 ?/. - c.455G>A r.(?) p.(Arg152Gln)
GDPD3 NM_024307.2 ?/. - c.-4959G>A r.(?) p.(=)


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