1-214019351-G-T

Variant names:

• chr1-214019351-G-T
• rs12081352
• NM_001270616.2:c.2028+7636G>T

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BS1 BS2

The NM_001270616.2(PROX1):​c.2028+7636G>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0243 in 152,188 control chromosomes in the GnomAD database, including 47 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 0.024 (47 hom., cov: 33)
• Consequence: PROX1 NM_001270616.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.46
• Publications: 3 publications found

Genes affected

PROX1 (HGNC:9459): (prospero homeobox 1) The protein encoded by this gene is a member of the homeobox transcription factor family. Members of this family contain a homeobox domain that consists of a 60-amino acid helix-turn-helix structure that binds DNA and RNA. The protein encoded by this gene is conserved across vertebrates and may play an essential role during development. Altered levels of this protein have been reported in cancers of different organs, such as colon, brain, blood, breast, pancreas, liver and esophagus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BS1: Variant frequency is greater than expected in population afr. GnomAd4 allele frequency = 0.0243 (3701/152188) while in subpopulation AFR AF = 0.0362 (1503/41510). AF 95% confidence interval is 0.0347. There are 47 homozygotes in GnomAd4. There are 1847 alleles in the male GnomAd4 subpopulation. Median coverage is 33. This position passed quality control check.
• BS2: High AC in GnomAd4 at 3701 AD gene.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001270616.2. 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
	PROX1	NM_001270616.2	MANE Select	c.2028+7636G>T		intron	N/A	NP_001257545.1
	PROX1	NM_002763.5		c.2028+7636G>T		intron	N/A	NP_002754.2

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PROX1	ENST00000366958.9	TSL:1 MANE Select	c.2028+7636G>T		intron	N/A	ENSP00000355925.4
	PROX1	ENST00000435016.2	TSL:1	c.2028+7636G>T		intron	N/A	ENSP00000400694.1

Frequencies

GnomAD3 genomes AF: 0.0242 AC: 3682 AN: 152070 Hom.: 45 Cov.: 33

Gnomad AFR AF: 0.0359

Gnomad AMI AF: 0.0274

Gnomad AMR AF: 0.0154

Gnomad ASJ AF: 0.00807

Gnomad EAS AF: 0.0102

Gnomad SAS AF: 0.00455

Gnomad FIN AF: 0.0414

Gnomad MID AF: 0.0158

Gnomad NFE AF: 0.0197

Gnomad OTH AF: 0.0249

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

GnomAD4 genome AF: 0.0243 AC: 3701 AN: 152188 Hom.: 47 Cov.: 33 AF XY: 0.0248 AC XY: 1847 AN XY: 74408

African (AFR) AF: 0.0362 AC: 1503 AN: 41510

American (AMR) AF: 0.0154 AC: 235 AN: 15284

Ashkenazi Jewish (ASJ) AF: 0.00807 AC: 28 AN: 3470

East Asian (EAS) AF: 0.0102 AC: 53 AN: 5176

South Asian (SAS) AF: 0.00456 AC: 22 AN: 4828

European-Finnish (FIN) AF: 0.0414 AC: 438 AN: 10592

Middle Eastern (MID) AF: 0.0170 AC: 5 AN: 294

European-Non Finnish (NFE) AF: 0.0197 AC: 1340 AN: 68012

Other (OTH) AF: 0.0246 AC: 52 AN: 2110

Alfa AF: 0.00886 Hom.: 2

Bravo AF: 0.0234

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	0.079
DANN	Benign	0.34
PhyloP100		-1.5
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.1
Mutation Taster		=100/0	polymorphism

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: rs12081352; hg19: chr1-214192694;