Variant #0000315859 (NC_000002.11:g.219566715C>G, NM_022453.2:c.-30022G>C (RNF25))

Chromosome 2
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.219566715C>G
DNA change (hg38) g.218701992C>G
Published as STK36(NM_015690.4):c.3931C>G (p.P1311A)
ISCN -
DB-ID STK36_000005
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STK36 NM_015690.4 ?/. - c.3931C>G r.(?) p.(Pro1311Ala)
RNF25 NM_022453.2 ?/. - c.-30022G>C r.(?) p.(=)


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