Variant #0000285156 (NC_000003.11:g.50338047G>A, NM_003549.3:c.-1421C>T (HYAL3))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.50338047G>A
DNA change (hg38) g.50300616G>A
Published as HYAL1(NM_153281.1):c.1175C>T (p.T392M)
ISCN -
DB-ID HYAL1_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) 0.00608 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.-1421C>T r.(?) p.(=)
NAT6 NM_012191.3 -/. - c.-1402C>T r.(?) p.(=)
HYAL1 NM_033159.2 -/. - c.1175C>T r.(?) p.(Thr392Met)


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