Variant #0000608721 (NC_000003.11:g.4459755C>G, NM_182760.3:c.664G>C (SUMF1))

Chromosome 3
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.4459755C>G
DNA change (hg38) g.4418071C>G
Published as SUMF1(NM_001164674.1):c.589G>C (p.(Gly197Arg)), SUMF1(NM_182760.3):c.664G>C (p.G222R)
ISCN -
DB-ID SUMF1_000007 See all 4 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) 0.00167 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SUMF1 NM_182760.3 ?/. - c.664G>C r.(?) p.(Gly222Arg)


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