Variant #0000576287 (NC_000023.10:g.48775899C>G, NM_006875.3:c.85G>C (PIM2))

Chromosome X
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.48775899C>G
DNA change (hg38) g.48918622C>G
Published as PIM2(NM_006875.3):c.85G>C (p.E29Q)
ISCN -
DB-ID PIM2_000009
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) 2.0E-5 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIM2 NM_006875.3 ?/. - c.85G>C r.(?) p.(Glu29Gln)
OTUD5 NM_017602.3 ?/. - c.*4552G>C r.(=) p.(=)


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