Variant #0000282264 (NC_000017.10:g.78354661C>T, NM_001256071.1:c.13671C>T (RNF213))

Chromosome 17
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.78354661C>T
DNA change (hg38) g.80380861C>T
Published as RNF213(NM_001256071.3):c.13671C>T (p.H4557=), RNF213-AS1(NR_029376.1):n.241-25573G>A
ISCN -
DB-ID RNF213_000019
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) 0.76488 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RNF213 NM_001256071.1 -/. - c.13671C>T r.(?) p.(His4557=)
ENDOV NM_173627.3 -/. - c.-34334C>T r.(?) p.(=)


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