rs7753873

Variant names:

• chr6-137852285-A-C
• rs7753873
• ENST00000606998.2:n.1056+12874T>G

Variant summary

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

The ENST00000606998.2(WAKMAR2):​n.1056+12874T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.178 in 152,032 control chromosomes in the GnomAD database, including 4,123 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 (4123 hom., cov: 32)
• Consequence: WAKMAR2 ENST00000606998.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.999
• Publications: 23 publications found

Genes affected

WAKMAR2 (HGNC:53754): (wound and keratinocyte migration associated lncRNA 2)

ENSG00000299400 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.94).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.412 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000606998.2. 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
	WAKMAR2	NR_049793.1		n.1056+12874T>G		intron	N/A

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	WAKMAR2	ENST00000606998.2	TSL:2	n.1056+12874T>G		intron	N/A
	WAKMAR2	ENST00000763029.1		n.592+15357T>G		intron	N/A
	WAKMAR2	ENST00000763030.1		n.187+3103T>G		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.178 AC: 27010 AN: 151914 Hom.: 4098 Cov.: 32

Gnomad AFR AF: 0.417

Gnomad AMI AF: 0.0879

Gnomad AMR AF: 0.158

Gnomad ASJ AF: 0.120

Gnomad EAS AF: 0.0623

Gnomad SAS AF: 0.0997

Gnomad FIN AF: 0.0253

Gnomad MID AF: 0.158

Gnomad NFE AF: 0.0798

Gnomad OTH AF: 0.162

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

GnomAD4 genome AF: 0.178 AC: 27085 AN: 152032 Hom.: 4123 Cov.: 32 AF XY: 0.172 AC XY: 12808 AN XY: 74300

African (AFR) AF: 0.417 AC: 17292 AN: 41450

American (AMR) AF: 0.157 AC: 2402 AN: 15262

Ashkenazi Jewish (ASJ) AF: 0.120 AC: 414 AN: 3462

East Asian (EAS) AF: 0.0626 AC: 324 AN: 5174

South Asian (SAS) AF: 0.0990 AC: 476 AN: 4810

European-Finnish (FIN) AF: 0.0253 AC: 268 AN: 10574

Middle Eastern (MID) AF: 0.153 AC: 45 AN: 294

European-Non Finnish (NFE) AF: 0.0798 AC: 5428 AN: 67986

Other (OTH) AF: 0.169 AC: 356 AN: 2110

Alfa AF: 0.151 Hom.: 684

Bravo AF: 0.197

Asia WGS AF: 0.148 AC: 517 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.94
CADD	Benign	0.082
DANN	Benign	0.41
PhyloP100		-1.0
Mutation Taster		=100/0	polymorphism (auto)

Splicing

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

MaxEntScan Visualizer can be used to analyze the impact of this mutation on the neighboring sequence.

Other links and lift over

dbSNP: rs7753873;

hg19: chr6-138173422;

COSMIC: COSV74118445;