Variant #0001041622 (NC_000017.10:g.1399420dup, NM_001080779.1:c.-3639dup (MYO1C))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.1399420dup
DNA change (hg38) -
Published as INPP5K(NM_016532.4):c.1224dup (p.(Glu409*))
ISCN -
DB-ID INPP5K_000015
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 2025-05-05 21:14:00 +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     
MYO1C NM_001080779.1 ?/. - c.-3639dup r.(?) p.(=)
INPP5K NM_001135642.1 ?/. - c.996dup r.(?) p.(Glu333*)
INPP5K NM_016532.3 ?/. - c.1224dup r.(?) p.(Glu409*)


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