Variant #0000929474 (NC_000008.10:g.70515476A>G, NM_015170.2:c.1111A>G (SULF1))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.70515476A>G
DNA change (hg38) -
Published as SULF1(NM_001128204.1):c.1111A>G (p.(Ile371Val)), SULF1(NM_001128205.2):c.1111A>G (p.I371V), SULF1(NM_015170.2):c.1111A>G (p.I371V)
ISCN -
DB-ID SULF1_000002 See all 3 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) 0.00387 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 2023-07-07 10:10:56 +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     
SULF1 NM_015170.2 -?/. - c.1111A>G r.(?) p.(Ile371Val)


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