Variant #0001035609 (NC_000006.11:g.167369655G>A, NM_003730.4:c.16C>T (RNASET2))

Chromosome 6
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.167369655G>A
DNA change (hg38) -
Published as RNASET2(NM_003730.5):c.16C>T (p.L6=), RNASET2(NM_003730.6):c.16C>T (p.(Leu6=))
ISCN -
DB-ID RNASET2_000016 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) 0.0059 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 2025-05-05 21:14:00 +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     
RNASET2 NM_003730.4 -?/. - c.16C>T r.(?) p.(Leu6=)


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