Variant #0000999246 (NC_000011.9:g.64534518_64534520del, NM_004630.3:c.1449_1451del (SF1))

Chromosome 11
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.64534518_64534520del
DNA change (hg38) -
Published as SF1(NM_004630.3):c.1449_1451delGCC (p.(Pro484del)), SF1(NM_201995.3):c.1449_1451delGCC (p.P485del)
ISCN -
DB-ID SF1_000009 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 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     
SF1 NM_004630.3 ?/. - c.1449_1451del r.(?) p.(Pro485del)


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