Variant #0000889681 (NC_000011.9:g.125769731A>G, NC_000011.9(NM_031307.3):c.-47+3334T>C (PUS3))

Chromosome 11
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.125769731A>G
DNA change (hg38) -
Published as HYLS1(NM_001134793.1):c.468A>G (p.L156=), HYLS1(NM_145014.2):c.468A>G (p.L156=)
ISCN -
DB-ID HYLS1_000008 See all 2 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) 0.00227 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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HYLS1 NM_001134793.1 -?/. - c.468A>G r.(?) p.(Leu156=)
DDX25 NM_013264.4 -?/. - c.-4682A>G r.(?) p.(=)
PUS3 NM_031307.3 -?/. - c.-47+3334T>C r.(=) p.(=)
HYLS1 NM_145014.2 -?/. - c.468A>G r.(?) p.(Leu156=)


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