Variant #0000677060 (NC_000003.11:g.50334695C>G, NC_000003.11(NM_003549.3):c.-17-1645G>C (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.50334695C>G
DNA change (hg38) -
Published as NAA80(NM_001200016.1):c.200G>C (p.R67P)
ISCN -
DB-ID C3orf45_000005
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HYAL3 NM_003549.3 -?/. - c.-17-1645G>C r.(=) p.(=)
IFRD2 NM_006764.4 -?/. - c.-4798G>C r.(?) p.(=)
NAT6 NM_012191.3 -?/. - c.266G>C r.(?) p.(Arg89Pro)
HYAL1 NM_033159.2 -?/. - c.*3219G>C r.(=) p.(=)
C3orf45 NM_153215.1 -?/. - c.*10062C>G r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.