Variant #0000518506 (NC_000003.11:g.172165689A>G, NM_004122.2:c.515T>C (GHSR))

Chromosome 3
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.172165689A>G
DNA change (hg38) g.172447899A>G
Published as GHSR(NM_004122.2):c.515T>C (p.(Phe172Ser)), GHSR(NM_198407.2):c.515T>C (p.F172S)
ISCN -
DB-ID GHSR_000008 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) 1.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-10-29 20:49:11 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GHSR NM_004122.2 -?/. - c.515T>C r.(?) p.(Phe172Ser)


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