rs9292854

Variant names:

• chr5-42611718-G-C
• rs9292854
• NM_000163.5:c.71-17320G>C

Your query was ambiguous. Multiple possible variants found:

• chr5-42611718-G-C
• chr5-42611718-G-T

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_000163.5(GHR):​c.71-17320G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.233 in 152,004 control chromosomes in the GnomAD database, including 4,859 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.23 (4859 hom., cov: 32)
• Consequence: GHR NM_000163.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.380
• Publications: 3 publications found

Genes affected

GHR (HGNC:4263): (growth hormone receptor) This gene encodes a member of the type I cytokine receptor family, which is a transmembrane receptor for growth hormone. Binding of growth hormone to the receptor leads to receptor dimerization and the activation of an intra- and intercellular signal transduction pathway leading to growth. Mutations in this gene have been associated with Laron syndrome, also known as the growth hormone insensitivity syndrome (GHIS), a disorder characterized by short stature. In humans and rabbits, but not rodents, growth hormone binding protein (GHBP) is generated by proteolytic cleavage of the extracellular ligand-binding domain from the mature growth hormone receptor protein. Multiple alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Jun 2011]

GHR Gene-Disease associations (from GenCC):

• Laron syndrome

  Inheritance: AR Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Orphanet, Labcorp Genetics (formerly Invitae), G2P
• short stature due to partial GHR deficiency

  Inheritance: Unknown, AD Classification: STRONG, SUPPORTIVE Submitted by: Orphanet, Labcorp Genetics (formerly Invitae)

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.368 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_000163.5. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GHR	NM_000163.5	MANE Select	c.71-17320G>C		intron	N/A	NP_000154.1
	GHR	NM_001242399.2		c.92-17320G>C		intron	N/A	NP_001229328.1
	GHR	NM_001242400.2		c.71-17320G>C		intron	N/A	NP_001229329.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GHR	ENST00000230882.9	TSL:1 MANE Select	c.71-17320G>C		intron	N/A	ENSP00000230882.4
	GHR	ENST00000620156.4	TSL:5	c.92-17320G>C		intron	N/A	ENSP00000483403.1
	GHR	ENST00000537449.5	TSL:5	c.71-17320G>C		intron	N/A	ENSP00000442206.2

Frequencies

GnomAD3 genomes AF: 0.233 AC: 35361 AN: 151886 Hom.: 4856 Cov.: 32

Gnomad AFR AF: 0.373

Gnomad AMI AF: 0.275

Gnomad AMR AF: 0.161

Gnomad ASJ AF: 0.152

Gnomad EAS AF: 0.00212

Gnomad SAS AF: 0.0750

Gnomad FIN AF: 0.252

Gnomad MID AF: 0.191

Gnomad NFE AF: 0.194

Gnomad OTH AF: 0.214

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.233 AC: 35379 AN: 152004 Hom.: 4859 Cov.: 32 AF XY: 0.231 AC XY: 17182 AN XY: 74316

African (AFR) AF: 0.373 AC: 15448 AN: 41446

American (AMR) AF: 0.161 AC: 2457 AN: 15272

Ashkenazi Jewish (ASJ) AF: 0.152 AC: 528 AN: 3470

East Asian (EAS) AF: 0.00213 AC: 11 AN: 5174

South Asian (SAS) AF: 0.0753 AC: 363 AN: 4820

European-Finnish (FIN) AF: 0.252 AC: 2661 AN: 10558

Middle Eastern (MID) AF: 0.195 AC: 57 AN: 292

European-Non Finnish (NFE) AF: 0.194 AC: 13156 AN: 67956

Other (OTH) AF: 0.213 AC: 448 AN: 2106

Alfa AF: 0.221 Hom.: 523

Bravo AF: 0.232

Asia WGS AF: 0.0590 AC: 208 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	1.5
DANN	Benign	0.63
PhyloP100		0.38
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs9292854; hg19: chr5-42611820;