Variant #0000325162 (NC_000017.10:g.7534998G>A, NM_004860.3:c.-17148C>T (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.7534998G>A
DNA change (hg38) g.7631680G>A
Published as SHBG(NM_001040.4):c.647G>A (p.(Ser216Asn))
ISCN -
DB-ID SHBG_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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SHBG NM_001040.3 ?/. - c.647G>A r.(?) p.(Ser216Asn)
FXR2 NM_004860.3 ?/. - c.-17148C>T r.(?) p.(=)
SAT2 NM_133491.3 ?/. - c.-4045C>T r.(?) p.(=)


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