Variant #0000720957 (NC_000006.11:g.43638600T>A, NM_152732.4:c.745T>A (RSPH9))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.43638600T>A
DNA change (hg38) -
Published as RSPH9(NM_001193341.1):c.797T>A (p.L266H)
ISCN -
DB-ID MRPS18A_000005
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) 0.00019 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 2021-02-08 18:36:18 +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.*899A>T r.(=) p.(=)
RSPH9 NM_152732.4 ?/. - c.745T>A r.(?) p.(Phe249Ile)


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