Variant #0000561170 (NC_000017.10:g.36487039C>G, NM_001004334.2:c.2413G>C (GPR179))

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.36487039C>G
DNA change (hg38) g.38331156C>G
Published as GPR179(NM_001004334.3):c.2413G>C (p.E805Q), GPR179(NM_001004334.4):c.2413G>C (p.E805Q)
ISCN -
DB-ID GPR179_000034 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) 0.00139 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
GPR179 NM_001004334.2 -?/. - c.2413G>C r.(?) p.(Glu805Gln)


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