Variant #0000304651 (NC_000002.11:g.18736950T>C, NM_001002006.2:c.*8112A>G (NT5C1B))

Chromosome 2
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.18736950T>C
DNA change (hg38) g.18555684T>C
Published as NT5C1B-RDH14(NM_001199103.1):c.1460A>G (p.N487S)
ISCN -
DB-ID NT5C1B-RDH14_000001
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) 0.00024 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 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NT5C1B NM_001002006.2 -?/. - c.*8112A>G r.(=) p.(=)
NT5C1B-RDH14 NM_001199103.1 -?/. - c.1460A>G r.(?) p.(Asn487Ser)
RDH14 NM_020905.3 -?/. - c.518A>G r.(?) p.(Asn173Ser)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.