Variant #0000806891 (NC_000015.9:g.72109968C>T, NM_014249.3:c.1176C>T (NR2E3))

Chromosome 15
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.72109968C>T
DNA change (hg38) -
Published as NR2E3(NM_014249.4):c.1176C>T (p.R392=)
ISCN -
DB-ID MYO9A_000018
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) 0 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYO9A NM_006901.3 -?/. - c.*8953G>A r.(=) p.(=)
NR2E3 NM_014249.3 -?/. - c.1176C>T r.(?) p.(Arg392=)


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