Variant #0000330540 (NC_000005.9:g.138286942dup, NM_001037633.1:c.947dup (SIL1))

Chromosome 5
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.138286942dup
DNA change (hg38) g.138951253dup
Published as SIL1(NM_001037633.1):c.947_948insT (p.(Arg317GlufsTer35)), SIL1(NM_001037633.1):c.947dupT (p.R317Efs*35)
ISCN -
DB-ID SIL1_000013 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-17 15:29:06 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SIL1 NM_001037633.1 ?/. - c.947dup r.(?) p.(Arg317GlufsTer35)


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