rs7155936

Variant names:

• chr14-55182172-A-C
• rs7155936
• NM_014750.5:c.495+198T>G

Your query was ambiguous. Multiple possible variants found:

• chr14-55182172-A-C
• chr14-55182172-A-T

Variant summary

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

The NM_014750.5(DLGAP5):​c.495+198T>G variant causes a intron 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. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 32)
• Consequence: DLGAP5 NM_014750.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0330

Genes affected

DLGAP5 (HGNC:16864): (DLG associated protein 5) Predicted to enable microtubule binding activity. Predicted to be involved in several processes, including centrosome localization; kinetochore assembly; and mitotic spindle organization. Located in several cellular components, including centrosome; cytosol; and mitochondrion. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Likely_benign. Variant got -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
DLGAP5	NM_014750.5	c.495+198T>G		intron_variant	Intron 4 of 18	ENST00000247191.7	NP_055565.3
DLGAP5	NM_001146015.2	c.495+198T>G		intron_variant	Intron 4 of 19		NP_001139487.1
DLGAP5	XM_017021840.3	c.495+198T>G		intron_variant	Intron 4 of 18		XP_016877329.1
DLGAP5	XM_047432016.1	c.495+198T>G		intron_variant	Intron 4 of 19		XP_047287972.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
DLGAP5	ENST00000247191.7	c.495+198T>G		intron_variant	Intron 4 of 18	1	NM_014750.5	ENSP00000247191.2
DLGAP5	ENST00000395425.6	c.495+198T>G		intron_variant	Intron 4 of 19	1		ENSP00000378815.2
DLGAP5	ENST00000557645.5	c.495+198T>G		intron_variant	Intron 4 of 5	3		ENSP00000451747.1

Frequencies

GnomAD3 genomes Cov.: 32

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

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	1.3
DANN	Benign	0.46

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: rs7155936; hg19: chr14-55648890;