Variant #0000975476 (NC_000002.11:g.99172084_99172098del, NM_001134225.1:c.1635_1649del (INPP4A))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.99172084_99172098del
DNA change (hg38) -
Published as INPP4A(NM_001134225.2):c.1635_1649del (p.(Gln545_Leu549del))
ISCN -
DB-ID INPP4A_000010
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INPP4A NM_001134225.1 -?/. - c.1635_1649del r.(?) p.(Gln545_Leu549del)
INPP4A NM_001566.2 -?/. - c.1650_1664del r.(?) p.(Gln550_Leu554del)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.