Variant #0000802614 (NC_000006.11:g.43612837T>C, NM_152732.4:c.2T>C (RSPH9))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.43612837T>C
DNA change (hg38) -
Published as RSPH9(NM_152732.5):c.2T>C (p.M1?)
ISCN -
DB-ID RSPH9_000007 See all 2 reported entries
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) 3.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-09-17 14:40:49 +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.*4567T>C r.(=) p.(=)
MRPS18A NM_018135.3 +/. - c.*26662A>G r.(=) p.(=)
RSPH9 NM_152732.4 +/. - c.2T>C r.(?) p.(Met1?)


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