Variant #0000520279 (NC_000003.11:g.50332501C>T, NM_003549.3:c.533G>A (HYAL3))

Chromosome 3
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.50332501C>T
DNA change (hg38) g.50295070C>T
Published as HYAL3(NM_001200029.1):c.533G>A (p.(Arg178His))
ISCN -
DB-ID C3orf45_000002
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) 0.00543 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HYAL3 NM_003549.3 -?/. - c.533G>A r.(?) p.(Arg178His)
IFRD2 NM_006764.4 -?/. - c.-2604G>A r.(?) p.(=)
NAT6 NM_012191.3 -?/. - c.*1533G>A r.(=) p.(=)
HYAL1 NM_033159.2 -?/. - c.*5413G>A r.(=) p.(=)
C3orf45 NM_153215.1 -?/. - c.*7868C>T r.(=) p.(=)


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