NM_006640.5:c.-134G>C

Variant names:

• chr17-77320193-G-C
• rs80338760
• NM_006640.5:c.-134G>C

Variant summary

Our verdict is Uncertain significance. Variant got 2 ACMG points: 3P and 1B. PM2 PP5 BP4

The NM_006640.5(SEPTIN9):​c.-134G>C variant causes a 5 prime UTR change. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Pathogenic (no stars).

• Frequency: Genomes: not found (cov: 32)
• Consequence: SEPTIN9 NM_006640.5 5_prime_UTR
• Clinical Significance: Pathogenic no assertion criteria provided P:1 O:1
• Conservation: PhyloP100: 7.19

Genes affected

SEPTIN9 (HGNC:7323): (septin 9) This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Mar 2009]

ACMG classification

Verdict is Uncertain_significance. Variant got 2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• PP5: Variant 17-77320193-G-C is Pathogenic according to our data. Variant chr17-77320193-G-C is described in ClinVar as [Pathogenic]. Clinvar id is 5865.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr17-77320193-G-C is described in Lovd as [Pathogenic].
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.38). . Strength limited to SUPPORTING due to the PP5.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SEPTIN9	NM_006640.5	c.-134G>C		5_prime_UTR_variant	Exon 1 of 11	ENST00000329047.13	NP_006631.2
SEPTIN9	NM_001113491.2	c.76+12996G>C		intron_variant	Intron 2 of 11	ENST00000427177.6	NP_001106963.1
SEPTIN9	NM_001293695.2	c.19+38639G>C		intron_variant	Intron 1 of 10		NP_001280624.1
SEPTIN9	NM_001113492.2	c.-417+12996G>C		intron_variant	Intron 2 of 11		NP_001106964.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
SEPTIN9	ENST00000329047	c.-134G>C		5_prime_UTR_variant	Exon 1 of 11	1	NM_006640.5	ENSP00000329161.8
SEPTIN9	ENST00000427177.6	c.76+12996G>C		intron_variant	Intron 2 of 11	1	NM_001113491.2	ENSP00000391249.1

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 32

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:1 Other:1

Revision: no assertion criteria provided

Submissions by phenotype

Amyotrophic neuralgia Pathogenic:1 Other:1

Oct 01, 2005

OMIM

Significance: Pathogenic

Review Status: no assertion criteria provided

Collection Method: literature only

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GeneReviews

Significance: not provided

Review Status: no classification provided

Collection Method: literature only

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.38
CADD	Benign	20
DANN	Benign	0.92

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

LitVar

Other links and lift over

dbSNP: rs80338760; hg19: chr17-75316275;