Variant #0000555309 (NC_000015.9:g.72109963_72109964del, NM_014249.3:c.1171_1172del (NR2E3))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.72109963_72109964del
DNA change (hg38) g.71817622_71817623del
Published as -
ISCN -
DB-ID MYO9A_000003 See all 4 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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYO9A NM_006901.3 +/. - c.*8960_*8961del r.(=) p.(=)
NR2E3 NM_014249.3 +/. - c.1171_1172del r.(?) p.(Phe391ProfsTer15)


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