Variant #0000247955 (NC_000006.11:g.167344583A>G, NM_003730.4:c.516T>C (RNASET2))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.167344583A>G
DNA change (hg38) g.166931095A>G
Published as RNASET2(NM_003730.5):c.516T>C (p.L172=), RNASET2(NM_003730.6):c.516T>C (p.L172=)
ISCN -
DB-ID RNASET2_000007 See all 3 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) 0.1639 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RNASET2 NM_003730.4 -/. - c.516T>C r.(?) p.(Leu172=)


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