Variant #0000565621 (NC_000019.9:g.11034685dup, NC_000019.9(NM_024029.3):c.485-3dup (YIPF2))

Chromosome 19
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.11034685dup
DNA change (hg38) g.10924009dup
Published as YIPF2(NM_024029.4):c.485-3dupC
ISCN -
DB-ID C19orf52_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 2020-07-15 11:49:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
YIPF2 NM_024029.3 -/. - c.485-3dup r.spl? p.?
C19orf52 NM_138358.2 -/. - c.-4814dup r.(?) p.(=)
CARM1 NM_199141.1 -/. - c.*2252dup r.(?) p.(=)


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