Variant #0000295883 (NC_000017.10:g.8192922C>T, NC_000017.10(NM_016492.4):c.437+16C>T (RANGRF))

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.8192922C>T
DNA change (hg38) g.8289604C>T
Published as RANGRF(NM_001177802.2):c.*43C>T, RANGRF(NM_016492.5):c.437+16C>T, SLC25A35(NM_201520.3):c.*12G>A
ISCN -
DB-ID RANGRF_000008 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) 0.10712 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
RANGRF NM_016492.4 -/. - c.437+16C>T r.(=) p.(=)
SLC25A35 NM_201520.1 -/. - c.*12G>A r.(=) p.(=)


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