Variant #0000520280 (NC_000003.11:g.50334551T>C, NC_000003.11(NM_003549.3):c.-17-1501A>G (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.50334551T>C
DNA change (hg38) g.50297120T>C
Published as NAT6(NM_001200016.1):c.344A>G (p.(Glu115Gly))
ISCN -
DB-ID C3orf45_000003
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 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.-17-1501A>G r.(=) p.(=)
IFRD2 NM_006764.4 -?/. - c.-4654A>G r.(?) p.(=)
NAT6 NM_012191.3 -?/. - c.410A>G r.(?) p.(Glu137Gly)
HYAL1 NM_033159.2 -?/. - c.*3363A>G r.(=) p.(=)
C3orf45 NM_153215.1 -?/. - c.*9918T>C r.(=) p.(=)


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