Variant #0000924457 (NC_000006.11:g.167369650G>A, NM_003730.4:c.21C>T (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.167369650G>A
DNA change (hg38) -
Published as RNASET2(NM_003730.5):c.21C>T (p.R7=), RNASET2(NM_003730.6):c.21C>T (p.(Arg7=), p.R7=)
ISCN -
DB-ID RNASET2_000014 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) 0.04801 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +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.21C>T r.(?) p.(Arg7=)


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