NM_018145.3:c.1225-128A>G

Variant names:

• chr15-40737469-T-C
• rs2304580
• NM_018145.3:c.1225-128A>G

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_018145.3(RMDN3):​c.1225-128A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.198 in 1,145,010 control chromosomes in the GnomAD database, including 31,774 homozygotes. 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: 𝑓 0.18 (3806 hom., cov: 32)
  • Exomes 𝑓: 0.20 (27968 hom.)
• Consequence: RMDN3 NM_018145.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.928
• Publications: 23 publications found

Genes affected

RMDN3 (HGNC:25550): (regulator of microtubule dynamics 3) Enables microtubule binding activity. Involved in cellular calcium ion homeostasis. Located in several cellular components, including intercellular bridge; mitochondrial outer membrane; and spindle. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.77).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.673 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_018145.3. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	RMDN3	NM_018145.3	MANE Select	c.1225-128A>G		intron	N/A	NP_060615.1
	RMDN3	NM_001323896.2		c.1303-128A>G		intron	N/A	NP_001310825.1
	RMDN3	NM_001323897.2		c.1303-128A>G		intron	N/A	NP_001310826.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	RMDN3	ENST00000338376.8	TSL:1 MANE Select	c.1225-128A>G		intron	N/A	ENSP00000342493.3
	RMDN3	ENST00000260385.10	TSL:1	c.1225-128A>G		intron	N/A	ENSP00000260385.6
	RMDN3	ENST00000558777.5	TSL:2	n.*776-128A>G		intron	N/A	ENSP00000453357.1

Frequencies

GnomAD3 genomes AF: 0.180 AC: 27317 AN: 152028 Hom.: 3799 Cov.: 32

Gnomad AFR AF: 0.0855

Gnomad AMI AF: 0.235

Gnomad AMR AF: 0.340

Gnomad ASJ AF: 0.210

Gnomad EAS AF: 0.692

Gnomad SAS AF: 0.313

Gnomad FIN AF: 0.154

Gnomad MID AF: 0.152

Gnomad NFE AF: 0.154

Gnomad OTH AF: 0.198

GnomAD4 exome AF: 0.201 AC: 199169 AN: 992864 Hom.: 27968 Cov.: 13 AF XY: 0.201 AC XY: 102467 AN XY: 510120

African (AFR) AF: 0.0809 AC: 1887 AN: 23324

American (AMR) AF: 0.491 AC: 17228 AN: 35090

Ashkenazi Jewish (ASJ) AF: 0.212 AC: 4592 AN: 21612

East Asian (EAS) AF: 0.699 AC: 25857 AN: 37006

South Asian (SAS) AF: 0.267 AC: 19144 AN: 71580

European-Finnish (FIN) AF: 0.166 AC: 8486 AN: 51146

Middle Eastern (MID) AF: 0.178 AC: 747 AN: 4198

European-Non Finnish (NFE) AF: 0.159 AC: 112215 AN: 704436

Other (OTH) AF: 0.203 AC: 9013 AN: 44472

GnomAD4 genome AF: 0.180 AC: 27335 AN: 152146 Hom.: 3806 Cov.: 32 AF XY: 0.188 AC XY: 13982 AN XY: 74386

African (AFR) AF: 0.0854 AC: 3546 AN: 41508

American (AMR) AF: 0.340 AC: 5192 AN: 15260

Ashkenazi Jewish (ASJ) AF: 0.210 AC: 729 AN: 3468

East Asian (EAS) AF: 0.692 AC: 3578 AN: 5168

South Asian (SAS) AF: 0.313 AC: 1508 AN: 4816

European-Finnish (FIN) AF: 0.154 AC: 1634 AN: 10600

Middle Eastern (MID) AF: 0.160 AC: 47 AN: 294

European-Non Finnish (NFE) AF: 0.154 AC: 10467 AN: 68006

Other (OTH) AF: 0.198 AC: 420 AN: 2116

Alfa AF: 0.185 Hom.: 10946

Bravo AF: 0.198

Asia WGS AF: 0.460 AC: 1598 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.77
CADD	Benign	9.0
DANN	Benign	0.82
PhyloP100		0.93
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs2304580; hg19: chr15-41029667;