Variant #0000997488 (NC_000009.11:g.127617940_127617941del, NM_007209.3:c.*2256_*2257del (RPL35))

Chromosome 9
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.127617940_127617941del
DNA change (hg38) -
Published as WDR38(NM_001276374.1):c.218_219delCT (p.(Pro73fs))
ISCN -
DB-ID RPL35_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) 0.00033 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 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     
WDR38 NM_001045476.2 ?/. - c.218_219del r.(?) p.(Pro73Argfs*11)
RPL35 NM_007209.3 ?/. - c.*2256_*2257del r.(=) p.(=)


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