Variant #0000859953 (NC_000005.9:g.42695025T>A, NM_000163.4:c.273T>A (GHR))

Chromosome 5
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.42695025T>A
DNA change (hg38) -
Published as GHR(NM_000163.4):c.273T>A (p.(Thr91=)), GHR(NM_001242400.2):c.273T>A (p.T91=)
ISCN -
DB-ID GHR_000073 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) 0.00089 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 2022-05-09 15:51:19 +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     
GHR NM_000163.4 -?/. - c.273T>A r.(?) p.(Thr91=)


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