Variant #0000328971 (NC_000022.10:g.30419470G>A, NM_152510.2:c.-57048G>A (HORMAD2))

Chromosome 22
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.30419470G>A
DNA change (hg38) g.30023481G>A
Published as MTMR3(NM_153050.2):c.3339G>A (p.(=))
ISCN -
DB-ID MTMR3_000001
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) 0.00013 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MTMR3 NM_021090.3 ?/. - c.3425+784G>A r.(=) p.(=)
HORMAD2 NM_152510.2 ?/. - c.-57048G>A r.(?) p.(=)


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