Variant #0000518505 (NC_000003.11:g.172165673G>T, NM_004122.2:c.531C>A (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.172165673G>T
DNA change (hg38) g.172447883G>T
Published as GHSR(NM_004122.2):c.531C>A (p.(Pro177=)), GHSR(NM_198407.2):c.531C>A (p.P177=)
ISCN -
DB-ID GHSR_000007 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) 0.00343 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 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GHSR NM_004122.2 -?/. - c.531C>A r.(?) p.(Pro177=)


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