Variant #0000658193 (NC_000017.10:g.5342377C>A, NM_001033002.3:c.*6486C>A (RPAIN))

Chromosome 17
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.5342377C>A
DNA change (hg38) g.5439057C>A
Published as C1QBP(NM_001212.3):c.17G>T (p.(Arg6Leu))
ISCN -
DB-ID C1QBP_000003
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) 0.00069 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-03-23 16:13:27 +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     
RPAIN NM_001033002.3 -?/. - c.*6486C>A r.(=) p.(=)
C1QBP NM_001212.3 -?/. - c.17G>T r.(?) p.(Arg6Leu)
DHX33 NM_020162.3 -?/. - c.*5148G>T r.(=) p.(=)


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