Variant #0000800379 (NC_000002.11:g.219553458G>A, NM_022453.2:c.-16765C>T (RNF25))

Chromosome 2
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.219553458G>A
DNA change (hg38) -
Published as STK36(NM_015690.4):c.1419G>A (p.L473=)
ISCN -
DB-ID RNF25_000003
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) 0.00021 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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     
STK36 NM_015690.4 -?/. - c.1419G>A r.(?) p.(Leu473=)
RNF25 NM_022453.2 -?/. - c.-16765C>T r.(?) p.(=)


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