Variant #0000804208 (NC_000009.11:g.88356830_88356835dup, NM_015239.2:c.-170_-165dup (AGTPBP1))

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.88356830_88356835dup
DNA change (hg38) -
Published as AGTPBP1(NM_001286715.1):c.52_57dupGCCGCC (p.A18_A19dup), AGTPBP1(NM_001286717.1):c.52_57dupGCCGCC (p.(Ala18_Ala19dup))
ISCN -
DB-ID AGTPBP1_000016 See all 2 reported entries
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AGTPBP1 NM_015239.2 -/. - c.-170_-165dup r.(?) p.(=)


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