Variant #0000521136 (NC_000004.11:g.1087327_1087328insCTGCCCAGGCTGGAGCCAGCC, NC_000004.11(NM_194439.4):c.247-2702_247-2701insGGCTGGCTCCAGCCTGGGCAG (RNF212))

Chromosome 4
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.1087327_1087328insCTGCCCAGGCTGGAGCCAGCC
DNA change (hg38) g.1093539_1093540insCTGCCCAGGCTGGAGCCAGCC
Published as RNF212(NM_001193318.2):c.721_722insGGCTGGCTCCAGCCTGGGCAG (p.S241delins8)
ISCN -
DB-ID RNF212_000007
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RNF212 NM_001131034.3 -/. - c.247-2702_247-2701insGGCTGGCTCCAGCCTGGGCAG r.(=) p.(=)
RNF212 NM_194439.4 -/. - c.247-2702_247-2701insGGCTGGCTCCAGCCTGGGCAG r.(=) p.(=)


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