rs369206236

Variant names:

• chr5-173154406-A-G
• rs369206236
• NM_001205.3:c.262A>G

Your query was ambiguous. Multiple possible variants found:

• chr5-173154406-A-G
• chr5-173154406-A-T

Variant summary

Our verdict is Uncertain significance. The variant received 2 ACMG points: 2P and 0B. PM2

The NM_001205.3(BNIP1):​c.262A>G​(p.Met88Val) variant causes a missense change. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. M88L) has been classified as Uncertain significance.

• Frequency: Genomes: not found (cov: 32)
• Consequence: BNIP1 NM_001205.3 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 5.94
• Publications: 0 publications found

Genes affected

BNIP1 (HGNC:1082): (BCL2 interacting protein 1) This gene is a member of the BCL2/adenovirus E1B 19 kd-interacting protein (BNIP) family. It interacts with the E1B 19 kDa protein, which protects cells from virally-induced cell death. The encoded protein also interacts with E1B 19 kDa-like sequences of BCL2, another apoptotic protector. In addition, this protein is involved in vesicle transport into the endoplasmic reticulum. Alternative splicing of this gene results in four protein products with identical N- and C-termini. [provided by RefSeq, Mar 2011]

ACMG classification

Our verdict: Uncertain_significance. The variant received 2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001205.3. 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
	BNIP1	NM_001205.3	MANE Select	c.262A>G	p.Met88Val	missense	Exon 3 of 6	NP_001196.2	Q12981-4
	BNIP1	NM_013979.3		c.391A>G	p.Met131Val	missense	Exon 4 of 7	NP_053582.2	Q12981-1
	BNIP1	NM_013980.3		c.391A>G	p.Met131Val	missense	Exon 4 of 6	NP_053583.2	Q12981-3

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	BNIP1	ENST00000351486.10	TSL:1 MANE Select	c.262A>G	p.Met88Val	missense	Exon 3 of 6	ENSP00000239215.7	Q12981-4
	BNIP1	ENST00000231668.13	TSL:1	c.391A>G	p.Met131Val	missense	Exon 4 of 7	ENSP00000231668.9	Q12981-1
	BNIP1	ENST00000352523.10	TSL:1	c.391A>G	p.Met131Val	missense	Exon 4 of 6	ENSP00000239214.8	Q12981-3

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 30

GnomAD4 genome Cov.: 32

Alfa AF: 0.00 Hom.: 0

Bravo AF: 0.00000378

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.16
BayesDel_addAF	Pathogenic	0.16	D
BayesDel_noAF	Uncertain	0.0
CADD	Benign	22
DANN	Benign	0.96
DEOGEN2	Benign	0.095	T
Eigen	Benign	-0.057
Eigen_PC	Benign	0.064
FATHMM_MKL	Pathogenic	0.99	D
LIST_S2	Uncertain	0.91	D
M_CAP	Benign	0.025	T
MetaRNN	Benign	0.22	T
MetaSVM	Benign	-0.90	T
MutationAssessor	Uncertain	2.6	M
PhyloP100		5.9
PrimateAI	Uncertain	0.60	T
PROVEAN	Benign	-1.6	N
REVEL	Benign	0.24
Sift	Uncertain	0.024	D
Sift4G	Uncertain	0.028	D
Polyphen		0.056	B
Vest4		0.56
MutPred		0.31		Loss of catalytic residue at M88 (P = 0.0102)
MVP		0.39
MPC		0.36
ClinPred		0.78	D
GERP RS		4.4
Varity_R		0.35
gMVP		0.56
Mutation Taster		=48/52	disease causing

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.23		Details are displayed if max score is > 0.2
DS_DG_spliceai		0.23		Position offset: -1

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

Other links and lift over

dbSNP: rs369206236; hg19: chr5-172581409;