13-19467353-T-TA

Variant summary

Our verdict is Uncertain significance. Variant got 0 ACMG points: 0P and 0B.

The NM_001395978.1(TPTE2):​c.393-10dupT variant causes a intron change involving the alteration of a non-conserved nucleotide. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

Frequency

Genomes: 𝑓 0.0011 ( 0 hom., cov: 0)
Exomes 𝑓: 0.0041 ( 0 hom. )

Consequence

TPTE2
NM_001395978.1 intron

Scores

Not classified

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: 0.00
Variant links:
Genes affected
TPTE2 (HGNC:17299): (transmembrane phosphoinositide 3-phosphatase and tensin homolog 2) TPIP is a member of a large class of membrane-associated phosphatases with substrate specificity for the 3-position phosphate of inositol phospholipids.[supplied by OMIM, Jul 2002]

Genome browser will be placed here

ACMG classification

Classification made for transcript

Verdict is Uncertain_significance. Variant got 0 ACMG points.

Transcripts

RefSeq

Gene Transcript HGVSc HGVSp Effect #exon/exons MANE Protein UniProt
TPTE2NM_001395978.1 linkuse as main transcriptc.393-10dupT intron_variant ENST00000697147.1 NP_001382907.1

Ensembl

Gene Transcript HGVSc HGVSp Effect #exon/exons TSL MANE Protein Appris UniProt
TPTE2ENST00000697147.1 linkuse as main transcriptc.393-10dupT intron_variant NM_001395978.1 ENSP00000513136.1 Q6XPS3-1

Frequencies

GnomAD3 genomes
AF:
0.00105
AC:
138
AN:
131676
Hom.:
0
Cov.:
0
show subpopulations
Gnomad AFR
AF:
0.00174
Gnomad AMI
AF:
0.00
Gnomad AMR
AF:
0.00166
Gnomad ASJ
AF:
0.00
Gnomad EAS
AF:
0.00154
Gnomad SAS
AF:
0.00
Gnomad FIN
AF:
0.000454
Gnomad MID
AF:
0.00
Gnomad NFE
AF:
0.000608
Gnomad OTH
AF:
0.00331
GnomAD3 exomes
AF:
0.00618
AC:
202
AN:
32670
Hom.:
0
AF XY:
0.00597
AC XY:
101
AN XY:
16922
show subpopulations
Gnomad AFR exome
AF:
0.0136
Gnomad AMR exome
AF:
0.00663
Gnomad ASJ exome
AF:
0.000789
Gnomad EAS exome
AF:
0.00600
Gnomad SAS exome
AF:
0.00435
Gnomad FIN exome
AF:
0.00647
Gnomad NFE exome
AF:
0.00555
Gnomad OTH exome
AF:
0.0145
GnomAD4 exome
AF:
0.00405
AC:
4284
AN:
1057200
Hom.:
0
Cov.:
0
AF XY:
0.00412
AC XY:
2126
AN XY:
516382
show subpopulations
Gnomad4 AFR exome
AF:
0.00947
Gnomad4 AMR exome
AF:
0.00528
Gnomad4 ASJ exome
AF:
0.00465
Gnomad4 EAS exome
AF:
0.00282
Gnomad4 SAS exome
AF:
0.00414
Gnomad4 FIN exome
AF:
0.00649
Gnomad4 NFE exome
AF:
0.00375
Gnomad4 OTH exome
AF:
0.00505
GnomAD4 genome
AF:
0.00106
AC:
140
AN:
131678
Hom.:
0
Cov.:
0
AF XY:
0.00116
AC XY:
73
AN XY:
62962
show subpopulations
Gnomad4 AFR
AF:
0.00179
Gnomad4 AMR
AF:
0.00165
Gnomad4 ASJ
AF:
0.00
Gnomad4 EAS
AF:
0.00155
Gnomad4 SAS
AF:
0.00
Gnomad4 FIN
AF:
0.000454
Gnomad4 NFE
AF:
0.000608
Gnomad4 OTH
AF:
0.00330

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name
Calibrated prediction
Score
Prediction

Splicing

Name
Calibrated prediction
Score
Prediction
SpliceAI score (max)
0.060
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

Below is the list of publications found by LitVar. It may be empty.

Other links and lift over

dbSNP: rs71092363; hg19: chr13-20041493; API