2-79086426-T-C

Position:

• chr2-79086426-T-C

Variant summary

Our verdict is Likely benign. Variant got -4 ACMG points: 2P and 6B. PM2 BP4_Strong BP6_Moderate

The NM_006507.4(REG1B):​c.262A>G​(p.Ile88Val) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 15/21 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★).

• Frequency: Genomes: not found (cov: 32)
• Consequence: REG1B NM_006507.4 missense
• Clinical Significance: Likely benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -1.02

Genes affected

REG1B (HGNC:9952): (regenerating family member 1 beta) This gene is a type I subclass member of the Reg gene family. The Reg gene family is a multigene family grouped into four subclasses, types I, II, III and IV based on the primary structures of the encoded proteins. This gene encodes a protein secreted by the exocrine pancreas that is highly similar to the REG1A protein. The related REG1A protein is associated with islet cell regeneration and diabetogenesis, and may be involved in pancreatic lithogenesis. Reg family members REG1A, REGL, PAP and this gene are tandemly clustered on chromosome 2p12 and may have arisen from the same ancestral gene by gene duplication. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Likely_benign. Variant got -4 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.05795732).
• BP6: Variant 2-79086426-T-C is Benign according to our data. Variant chr2-79086426-T-C is described in ClinVar as [Likely_benign]. Clinvar id is 2267736.Status of the report is criteria_provided_single_submitter, 1 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
REG1B	NM_006507.4	c.262A>G	p.Ile88Val	missense_variant	4/6	ENST00000305089.8	NP_006498.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
REG1B	ENST00000305089.8	c.262A>G	p.Ile88Val	missense_variant	4/6	1	NM_006507.4	ENSP00000303206	P1
REG1B	ENST00000476554.1	n.674A>G		non_coding_transcript_exon_variant	3/3	1
REG1B	ENST00000479258.5	n.369A>G		non_coding_transcript_exon_variant	4/4	1
REG1B	ENST00000454188.5	c.115A>G	p.Ile39Val	missense_variant	2/4	3		ENSP00000387410

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 32

ClinVar

Significance: Likely benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not specified Benign:1

Likely benign, criteria provided, single submitter

clinical testing

Ambry Genetics

Dec 17, 2021

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity. -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.24
BayesDel_addAF	Benign	-0.33	T
BayesDel_noAF	Benign	-0.71
CADD	Benign	5.5
DANN	Benign	0.95
DEOGEN2	Benign	0.057	.;T
Eigen	Benign	-0.97
Eigen_PC	Benign	-0.94
FATHMM_MKL	Benign	0.0097	N
LIST_S2	Benign	0.59	T;T
M_CAP	Benign	0.00090	T
MetaRNN	Benign	0.058	T;T
MetaSVM	Benign	-0.93	T
MutationAssessor	Benign	0.35	.;N
MutationTaster	Benign	0.99	N
PrimateAI	Benign	0.37	T
PROVEAN	Benign	-0.040	N;N
REVEL	Benign	0.0070
Sift	Benign	0.38	T;T
Sift4G	Benign	0.28	T;T
Polyphen		0.15	.;B
Vest4		0.088
MutPred		0.45		.;Gain of catalytic residue at I88 (P = 0.0275);
MVP		0.088
MPC		0.011
ClinPred		0.14	T
GERP RS		0.70
Varity_R		0.040
gMVP		0.30

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

Publications

No publications associated with this variant yet.

Other links and lift over

hg19: chr2-79313552;