Variant #0000307392 (NC_000006.11:g.43638636G>A, NM_152732.4:c.781G>A (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.43638636G>A
DNA change (hg38) g.43670899G>A
Published as RSPH9(NM_001193341.1):c.833G>A (p.R278H)
ISCN -
DB-ID RSPH9_000006
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) 0.0765 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 2018-01-15 20:58:59 +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.*863C>T r.(=) p.(=)
RSPH9 NM_152732.4 -/. - c.781G>A r.(?) p.(Val261Ile)


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