Variant #0001052370 (NC_000006.11:g.43638575C>T, NM_152732.4:c.720C>T (RSPH9))

Chromosome 6
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.43638575C>T
DNA change (hg38) -
Published as RSPH9(NM_001193341.2):c.772C>T (p.(Gln258*))
ISCN -
DB-ID MRPS18A_000010
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) 4.0E-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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MRPS18A NM_018135.3 -?/. - c.*924G>A r.(=) p.(=)
RSPH9 NM_152732.4 -?/. - c.720C>T r.(?) p.(=)


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