NM_017858.3:c.815T>C

Variant names:

• chr15-66337049-A-G
• NM_017858.3:c.815T>C

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_017858.3(TIPIN):​c.815T>C​(p.Leu272Ser) variant causes a missense 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. 16/22 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).

• Frequency: Genomes: not found (cov: 32)
• Consequence: TIPIN NM_017858.3 missense
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: 0.147
• Publications: 0 publications found

Genes affected

TIPIN (HGNC:30750): (TIMELESS interacting protein) The protein encoded by this gene is part of the replisome complex, a group of proteins that support DNA replication. It binds TIM, which is involved in circadian rhythm regulation, and aids in protecting cells against DNA damage and stress. Two pseudogenes and two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]

ACMG classification

Our verdict: Likely_benign. The variant received -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.047694385).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_017858.3. 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
	TIPIN	NM_017858.3	MANE Select	c.815T>C	p.Leu272Ser	missense	Exon 8 of 8	NP_060328.3	Q9BVW5
	TIPIN	NM_001398281.1		c.815T>C	p.Leu272Ser	missense	Exon 8 of 8	NP_001385210.1	Q9BVW5
	TIPIN	NM_001398282.1		c.815T>C	p.Leu272Ser	missense	Exon 8 of 8	NP_001385211.1	Q9BVW5

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	TIPIN	ENST00000261881.9	TSL:1 MANE Select	c.815T>C	p.Leu272Ser	missense	Exon 8 of 8	ENSP00000261881.4	Q9BVW5
	TIPIN	ENST00000851323.1		c.815T>C	p.Leu272Ser	missense	Exon 8 of 8	ENSP00000521382.1
	TIPIN	ENST00000851324.1		c.815T>C	p.Leu272Ser	missense	Exon 7 of 7	ENSP00000521383.1

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 30

GnomAD4 genome Cov.: 32

ClinVar

ClinVar submissions

Significance: Uncertain significance

Revision: criteria provided, single submitter

Pathogenic	VUS	Benign	Condition
-	1	-	not specified (1)

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.066
BayesDel_addAF	Benign	-0.19	T
BayesDel_noAF	Benign	-0.52
CADD	Benign	9.0
DANN	Benign	0.72
DEOGEN2	Benign	0.0064	T
Eigen	Benign	-1.0
Eigen_PC	Benign	-1.1
FATHMM_MKL	Benign	0.052	N
LIST_S2	Benign	0.24	T
M_CAP	Benign	0.0044	T
MetaRNN	Benign	0.048	T
MetaSVM	Benign	-1.0	T
MutationAssessor	Benign	1.4	L
PhyloP100		0.15
PrimateAI	Benign	0.32	T
PROVEAN	Benign	-0.14	N
REVEL	Benign	0.046
Sift	Benign	0.19	T
Sift4G	Benign	0.69	T
Polyphen		0.089	B
Vest4		0.082
MutPred		0.13		Loss of stability (P = 0.0297)
MVP		0.23
MPC		0.15
ClinPred		0.094	T
GERP RS		1.0
Varity_R		0.044
gMVP		0.061

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

hg19: chr15-66629387;