Variant #0000249099 (NC_000006.11:g.43640099A>G, NM_152732.4:c.*1413A>G (RSPH9))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.43640099A>G
DNA change (hg38) g.43672362A>G
Published as MRPS18A(NM_018135.4):c.447-456T>C
ISCN -
DB-ID MRPS18A_000002
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) 0.15398 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MRPS18A NM_018135.3 -/. - c.447-456T>C r.(=) p.(=)
RSPH9 NM_152732.4 -/. - c.*1413A>G r.(=) p.(=)


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