Variant #0001043821 (NC_000022.10:g.31338205G>T, NM_001303256.2:c.480C>A (MORC2))

Chromosome 22
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.31338205G>T
DNA change (hg38) -
Published as MORC2(NM_001303256.3):c.480C>A (p.(Asp160Glu)), MORC2(NM_014941.3):c.294C>A (p.D98E)
ISCN -
DB-ID MORC2_000054 See all 2 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) 1.0E-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 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     
MORC2 NM_001303256.2 -?/. - c.480C>A r.(?) p.(Asp160Glu)


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