Variant #0001003055 (NC_000017.10:g.27042478del, NM_000984.5:c.-4546del (RPL23A))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.27042478del
DNA change (hg38) -
Published as RAB34(NM_031934.6):c.427delA (p.T143Pfs*9)
ISCN -
DB-ID PROCA1_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) 2.0E-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 2024-08-28 13:16:32 +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     
RPL23A NM_000984.5 +?/. - c.-4546del r.(?) p.(=)
RAB34 NM_031934.5 +?/. - c.427del r.(?) p.(Thr143Profs*9)
TLCD1 NM_138463.3 +?/. - c.*9050del r.(?) p.(=)
PROCA1 NM_152465.1 +?/. - c.-3800del r.(?) p.(=)


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