Variant #0000306062 (NC_000017.10:g.26684394T>G, NM_152464.1:c.-300T>G (TMEM199))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.26684394T>G
DNA change (hg38) g.28357369=
Published as POLDIP2(NM_015584.5):c.78A>C (p.*26Cext*343)
ISCN -
DB-ID POLDIP2_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) 0.99999 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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POLDIP2 NM_015584.3 -/. - c.81A>C r.(?) p.(Pro27=)
TNFAIP1 NM_021137.4 -/. - c.*12768T>G r.(=) p.(=)
TMEM199 NM_152464.1 -/. - c.-300T>G r.(?) p.(=)


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