Variant #0000610370 (NC_000006.11:g.43618165C>T, NM_152732.4:c.281C>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.43618165C>T
DNA change (hg38) g.43650428C>T
Published as RSPH9(NM_001193341.1):c.281C>T (p.A94V)
ISCN -
DB-ID MRPS18A_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) 5.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MRPS18A NM_018135.3 -?/. - c.*21334G>A r.(=) p.(=)
RSPH9 NM_152732.4 -?/. - c.281C>T r.(?) p.(Ala94Val)


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