Variant #0000307169 (NC_000004.11:g.1087514T>C, NC_000004.11(NM_194439.4):c.247-2888A>G (RNF212))

Chromosome 4
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.1087514T>C
DNA change (hg38) g.1093726T>C
Published as RNF212(NM_001193318.2):c.535A>G (p.I179V)
ISCN -
DB-ID RNF212_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) 0.00033 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 2018-01-15 20:58:59 +01:00 (CET)
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.247-2888A>G r.(=) p.(=)
RNF212 NM_194439.4 -?/. - c.247-2888A>G r.(=) p.(=)


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