rs4049879

Variant names:

• chr22-24614614-CAAAAAAAAAAAA-C
• rs4049879
• NM_001288833.2:c.165-156_165-145delAAAAAAAAAAAA

Your query was ambiguous. Multiple possible variants found:

• chr22-24614614-CAAAAAAAAAAAA-C
• chr22-24614614-CAAAAAAAAAAAA-CAA
• chr22-24614614-CAAAAAAAAAAAA-CAAA
• chr22-24614614-CAAAAAAAAAAAA-CAAAAA
• chr22-24614614-CAAAAAAAAAAAA-CAAAAAAAA
• chr22-24614614-CAAAAAAAAAAAA-CAAAAAAAAA
• chr22-24614614-CAAAAAAAAAAAA-CAAAAAAAAAA
• chr22-24614614-CAAAAAAAAAAAA-CAAAAAAAAAAA
• chr22-24614614-CAAAAAAAAAAAA-CAAAAAAAAAAAAA
• chr22-24614614-CAAAAAAAAAAAA-CAAAAAAAAAAAAAA
• chr22-24614614-CAAAAAAAAAAAA-CAAAAAAAAAAAAAAA
• chr22-24614614-CAAAAAAAAAAAA-CAAAAAAAAAAAAAAAA
• chr22-24614614-CAAAAAAAAAAAA-CAAAAAAAAAAAAAAAAA

Variant summary

Our verdict is Uncertain significance. The variant received 0 ACMG points: 0P and 0B.

The NM_001288833.2(GGT1):​c.165-156_165-145delAAAAAAAAAAAA variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00375 in 68,622 control chromosomes in the GnomAD database, with no homozygous occurrence. It is difficult to determine the true allele frequency of this variant because it is of type DEL_BIG, and the frequency of such variant types in population databases may be underestimated and unreliable. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.0037 (0 hom., cov: 29)
• Consequence: GGT1 NM_001288833.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.27
• Publications: 1 publications found

Genes affected

GGT1 (HGNC:4250): (gamma-glutamyltransferase 1) The enzyme encoded by this gene is a type I gamma-glutamyltransferase that catalyzes the transfer of the glutamyl moiety of glutathione to a variety of amino acids and dipeptide acceptors. The enzyme is composed of a heavy chain and a light chain, which are derived from a single precursor protein. It is expressed in tissues involved in absorption and secretion and may contribute to the etiology of diabetes and other metabolic disorders. Multiple alternatively spliced variants have been identified. There are a number of related genes present on chromosomes 20 and 22, and putative pseudogenes for this gene on chromosomes 2, 13, and 22. [provided by RefSeq, Jan 2014]

GGT1 Gene-Disease associations (from GenCC):

• gamma-glutamyl transpeptidase deficiency

  Inheritance: AR Classification: SUPPORTIVE, LIMITED Submitted by: Orphanet, Ambry Genetics

ENSG00000286070 (HGNC:):

ACMG classification

Our verdict: Uncertain_significance. The variant received 0 ACMG points.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001288833.2. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GGT1	NM_001288833.2	MANE Select	c.165-156_165-145delAAAAAAAAAAAA		intron	N/A	NP_001275762.1	P19440-1
	GGT1	NM_013421.3		c.165-156_165-145delAAAAAAAAAAAA		intron	N/A	NP_038265.2	A0A140VJJ9
	GGT1	NM_013430.3		c.165-156_165-145delAAAAAAAAAAAA		intron	N/A	NP_038347.2	P19440-1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GGT1	ENST00000400382.6	TSL:2 MANE Select	c.165-161_165-150delAAAAAAAAAAAA		intron	N/A	ENSP00000383232.1	P19440-1
	GGT1	ENST00000400380.5	TSL:1	c.165-161_165-150delAAAAAAAAAAAA		intron	N/A	ENSP00000383231.1	P19440-1
	ENSG00000286070	ENST00000652248.1		n.*655-161_*655-150delAAAAAAAAAAAA		intron	N/A	ENSP00000499210.1

Frequencies

GnomAD3 genomes AF: 0.00372 AC: 255 AN: 68606 Hom.: 0 Cov.: 29

Gnomad AFR AF: 0.0102

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.000685

Gnomad ASJ AF: 0.00

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.00

Gnomad FIN AF: 0.00

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.0000343

Gnomad OTH AF: 0.00442

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

GnomAD4 genome AF: 0.00375 AC: 257 AN: 68622 Hom.: 0 Cov.: 29 AF XY: 0.00348 AC XY: 112 AN XY: 32178

African (AFR) AF: 0.0102 AC: 248 AN: 24212

American (AMR) AF: 0.000685 AC: 4 AN: 5842

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 1716

East Asian (EAS) AF: 0.00 AC: 0 AN: 2052

South Asian (SAS) AF: 0.00 AC: 0 AN: 1854

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 2420

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 80

European-Non Finnish (NFE) AF: 0.0000343 AC: 1 AN: 29168

Other (OTH) AF: 0.00440 AC: 4 AN: 910

Alfa AF: 0.00 Hom.: 0

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
PhyloP100		1.3

Splicing

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

Other links and lift over

dbSNP: rs4049879; hg19: chr22-25010581;