Variant #0001000823 (NC_000014.8:g.21058683A>C, NM_145250.3:c.-450T>G (RNASE11))

Chromosome 14
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.21058683A>C
DNA change (hg38) -
Published as RNASE12(NM_001024822.2):c.200T>G (p.(Val67Gly))
ISCN -
DB-ID RNASE11_000004
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) 0.00053 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 2024-08-28 13:16:32 +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     
RNASE12 NM_001024822.2 ?/. - c.200T>G r.(?) p.(Val67Gly)
RNASE11 NM_145250.3 ?/. - c.-450T>G r.(?) p.(=)


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