Variant #0000862693 (NC_000011.9:g.71940703C>G, NC_000011.9(NM_001567.3):c.754-4C>G (INPPL1))

Chromosome 11
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.71940703C>G
DNA change (hg38) -
Published as INPPL1(NM_001567.3):c.754-4C>G (p.?)
ISCN -
DB-ID INPPL1_000033
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) 7.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INPPL1 NM_001567.3 -?/. - c.754-4C>G r.spl? p.?
PHOX2A NM_005169.3 -?/. - c.*10090G>C r.(=) p.(=)


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