Variant #0001003712 (NC_000017.10:g.7534934C>T, NM_004860.3:c.-17084G>A (FXR2))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.7534934C>T
DNA change (hg38) -
Published as SHBG(NM_001040.3):c.583C>T (p.(Arg195Cys))
ISCN -
DB-ID FXR2_000010
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SHBG NM_001040.3 ?/. - c.583C>T r.(?) p.(Arg195Cys)
FXR2 NM_004860.3 ?/. - c.-17084G>A r.(?) p.(=)
SAT2 NM_133491.3 ?/. - c.-3981G>A r.(?) p.(=)


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