Variant #0000075724 (NC_000013.10:g.29246545_29246546del, NM_015932.5:c.334_335del (POMP))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Probably affects function
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.29246545_29246546del
DNA change (hg38) g.28672408_28672409del
Published as 333_334delTA
ISCN -
DB-ID POMP_000002
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Timo Heß
Database submission license No license selected
Created by Timo Heß
Date created 2015-08-03 11:51:01 +02:00 (CEST)
Date last edited 2015-09-06 21:50:51 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POMP NM_015932.5 ?/+? 5 c.334_335del r.(?) p.(Ile112Trpfs*3)



Screenings

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