Variant #0000534851 (NC_000008.10:g.42706014C>T, NM_030954.3:c.*5288G>A (RNF170))

Chromosome 8
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.42706014C>T
DNA change (hg38) g.42850871C>T
Published as RNF170(NM_001160224.1):c.523G>A (p.D175N), RNF170(NM_001160224.2):c.523G>A (p.D175N)
ISCN -
DB-ID RNF170_000006 See all 2 reported entries
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) 0.00401 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RNF170 NM_030954.3 -/. - c.*5288G>A r.(=) p.(=)


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