Variant #0000929196 (NC_000006.11:g.43612973C>T, NM_152732.4:c.138C>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.43612973C>T
DNA change (hg38) -
Published as RSPH9(NM_152732.5):c.138C>T (p.F46=)
ISCN -
DB-ID MAD2L1BP_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) 1.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-07-07 10:10:56 +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     
MAD2L1BP NM_014628.2 -?/. - c.*4703C>T r.(=) p.(=)
MRPS18A NM_018135.3 -?/. - c.*26526G>A r.(=) p.(=)
RSPH9 NM_152732.4 -?/. - c.138C>T r.(?) p.(=)


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