Variant #0000537554 (NC_000009.11:g.140087050_140087052dup, NM_001128228.2:c.1842_1844dup (TPRN))

Chromosome 9
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.140087050_140087052dup
DNA change (hg38) g.137192598_137192600dup
Published as TPRN(NM_001128228.3):c.1842_1844dupGGA (p.E621dup)
ISCN -
DB-ID ANAPC2_000003
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPRN NM_001128228.2 -/. - c.1842_1844dup r.(?) p.(Glu621dup)
SSNA1 NM_003731.2 -/. - c.*2684_*2686dup r.(=) p.(=)
ANAPC2 NM_013366.3 -/. - c.-4043_-4041dup r.(?) p.(=)


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