rs941591

Variant names:

• chr14-94290413-T-A
• rs941591
• NM_001100607.3:c.181A>T

Your query was ambiguous. Multiple possible variants found:

• chr14-94290413-T-A
• chr14-94290413-T-C
• chr14-94290413-T-G

Variant summary

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

The NM_001100607.3(SERPINA10):​c.181A>T​(p.Ser61Cys) 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. 17/22 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 33)
• Consequence: SERPINA10 NM_001100607.3 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -4.21
• Publications: 31 publications found

Genes affected

SERPINA10 (HGNC:15996): (serpin family A member 10) The protein encoded by this gene belongs to the serpin family. It is predominantly expressed in the liver and secreted in plasma. It inhibits the activity of coagulation factors Xa and XIa in the presence of protein Z, calcium and phospholipid. Mutations in this gene are associated with venous thrombosis. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, May 2010]

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=0.060369372).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001100607.3. 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
	SERPINA10	NM_001100607.3	MANE Select	c.181A>T	p.Ser61Cys	missense	Exon 2 of 5	NP_001094077.1
	SERPINA10	NM_016186.3		c.181A>T	p.Ser61Cys	missense	Exon 2 of 5	NP_057270.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SERPINA10	ENST00000261994.9	TSL:1 MANE Select	c.181A>T	p.Ser61Cys	missense	Exon 2 of 5	ENSP00000261994.4
	SERPINA10	ENST00000554723.5	TSL:1	c.301A>T	p.Ser101Cys	missense	Exon 2 of 5	ENSP00000450896.1
	SERPINA10	ENST00000393096.5	TSL:1	c.181A>T	p.Ser61Cys	missense	Exon 2 of 5	ENSP00000376809.1

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome Cov.: 37

GnomAD4 genome Cov.: 33

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.11
BayesDel_addAF	Benign	-0.18	T
BayesDel_noAF	Benign	-0.49
CADD	Benign	0.083
DANN	Benign	0.51
DEOGEN2	Benign	0.052	T
Eigen	Benign	-2.0
Eigen_PC	Benign	-2.2
FATHMM_MKL	Benign	0.014	N
LIST_S2	Benign	0.36	T
M_CAP	Benign	0.0028	T
MetaRNN	Benign	0.060	T
MetaSVM	Benign	-0.93	T
MutationAssessor	Benign	0.0	N
PhyloP100		-4.2
PrimateAI	Benign	0.26	T
PROVEAN	Benign	-0.97	N
REVEL	Benign	0.28
Sift	Benign	0.050	D
Sift4G	Uncertain	0.039	D
Polyphen		0.46	P
Vest4		0.14
MutPred		0.23		Loss of phosphorylation at S61 (P = 0.0022)
MVP		0.17
MPC		0.026
ClinPred		0.10	T
GERP RS		-2.3
PromoterAI		0.037	Neutral
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.1
Varity_R		0.11
gMVP		0.39
Mutation Taster		=98/2	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: rs941591; hg19: chr14-94756750;