Variant #0000978528 (NC_000009.11:g.138395528G>A, NM_016034.4:c.440G>A (MRPS2))

Chromosome 9
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.138395528G>A
DNA change (hg38) -
Published as MRPS2(NM_016034.5):c.440G>A (p.(Arg147His))
ISCN -
DB-ID C9orf116_000004
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 2024-04-19 20:27:30 +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     
MRPS2 NM_016034.4 ?/. - c.440G>A r.(?) p.(Arg147His)
C9orf116 NM_144654.2 ?/. - c.-3831C>T r.(?) p.(=)


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