Variant #0000923868 (NC_000003.11:g.172165782C>G, NM_004122.2:c.422G>C (GHSR))

Chromosome 3
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.172165782C>G
DNA change (hg38) -
Published as GHSR(NM_004122.2):c.422G>C (p.(Arg141Pro)), GHSR(NM_198407.2):c.422G>C (p.R141P)
ISCN -
DB-ID GHSR_000010 See all 3 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) 3.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GHSR NM_004122.2 ?/. - c.422G>C r.(?) p.(Arg141Pro)


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