Variant #0000979432 (NC_000011.9:g.125769988G>A, NC_000011.9(NM_031307.3):c.-47+3077C>T (PUS3))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.125769988G>A
DNA change (hg38) -
Published as HYLS1(NM_001134793.2):c.725G>A (p.(Arg242Gln))
ISCN -
DB-ID HYLS1_000017
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) 5.0E-5 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 2024-04-19 20:27:30 +02:00 (CEST)
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.725G>A r.(?) p.(Arg242Gln)
DDX25 NM_013264.4 ?/. - c.-4425G>A r.(?) p.(=)
PUS3 NM_031307.3 ?/. - c.-47+3077C>T r.(=) p.(=)
HYLS1 NM_145014.2 ?/. - c.725G>A r.(?) p.(Arg242Gln)


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