Variant #0000294658 (NC_000017.10:g.8192133G>C, NM_016492.4:c.27G>C (RANGRF))

Chromosome 17
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.8192133G>C
DNA change (hg38) g.8288815G>C
Published as RANGRF(NM_001177802.2):c.27G>C (p.L9=), SLC25A35(NM_201520.3):c.*801C>G
ISCN -
DB-ID RANGRF_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) 0.00017 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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RANGRF NM_016492.4 -?/. - c.27G>C r.(?) p.(Leu9=)
SLC25A35 NM_201520.1 -?/. - c.*801C>G r.(=) p.(=)


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