rs551644836

Variant names:

• chr11-59125386-A-C
• rs551644836
• NM_198947.4:c.1289A>C

Your query was ambiguous. Multiple possible variants found:

• chr11-59125386-A-C
• chr11-59125386-A-G

Variant summary

Our verdict is Uncertain significance. Variant got 1 ACMG points: 2P and 1B. PM2 BP4

The NM_198947.4(FAM111B):​c.1289A>C​(p.Gln430Pro) 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. 13/21 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as not provided (no stars).

• Frequency: Genomes: not found (cov: 33)
• Consequence: FAM111B NM_198947.4 missense
• Clinical Significance: not provided no classification provided O:1
• Conservation: PhyloP100: 2.31

Genes affected

FAM111B (HGNC:24200): (FAM111 trypsin like peptidase B) This gene encodes a protein with a trypsin-like cysteine/serine peptidase domain in the C-terminus. Mutations in this gene are associated with an autosomal dominant form of hereditary fibrosing poikiloderma (HFP). Affected individuals display mottled pigmentation, telangiectasia, epidermal atrophy, tendon contractures, and progressive pulmonary fibrosis. Alternative splicing results in multiple transcript variants encoding distinct isoforms. A paralog of this gene which also has a trypsin‐like peptidase domain, FAM111A, is located only 16 kb from this gene on human chromosome 11q12.1. [provided by RefSeq, Apr 2014]

ACMG classification

Verdict is Uncertain_significance. Variant got 1 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.37101644).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
FAM111B	NM_198947.4	c.1289A>C	p.Gln430Pro	missense_variant	Exon 4 of 4	ENST00000343597.4	NP_945185.1
FAM111B	NM_001142703.2	c.1199A>C	p.Gln400Pro	missense_variant	Exon 3 of 3		NP_001136175.1
FAM111B	NM_001142704.2	c.1199A>C	p.Gln400Pro	missense_variant	Exon 2 of 2		NP_001136176.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
FAM111B	ENST00000343597.4	c.1289A>C	p.Gln430Pro	missense_variant	Exon 4 of 4	1	NM_198947.4	ENSP00000341565.3
FAM111B	ENST00000529618.5	c.1199A>C	p.Gln400Pro	missense_variant	Exon 3 of 3	1		ENSP00000432875.1
FAM111B	ENST00000620384.1	c.1289A>C	p.Gln430Pro	missense_variant	Exon 2 of 2	2		ENSP00000483456.1
FAM111B	ENST00000411426.1	c.1199A>C	p.Gln400Pro	missense_variant	Exon 2 of 2	4		ENSP00000393855.1

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome Cov.: 33

GnomAD4 genome Cov.: 33

ClinVar

Significance: not provided

Submissions summary: Other:1

Revision: no classification provided

Submissions by phenotype

Hereditary sclerosing poikiloderma with tendon and pulmonary involvement Other:1

-

GeneReviews

Significance: not provided

Review Status: no classification provided

Collection Method: literature only

May be associated with less severe extracutaneous phenotype. Further studies are needed. -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Uncertain	0.55
BayesDel_addAF	Benign	-0.10	T
BayesDel_noAF	Benign	-0.39
CADD	Benign	20
DANN	Benign	0.97
DEOGEN2	Benign	0.061	.;.;T;T
Eigen	Benign	-0.22
Eigen_PC	Benign	-0.41
FATHMM_MKL	Benign	0.45	N
LIST_S2	Benign	0.50	T;.;.;T
M_CAP	Benign	0.010	T
MetaRNN	Benign	0.37	T;T;T;T
MetaSVM	Benign	-1.0	T
MutationAssessor	Uncertain	2.3	.;.;M;M
PrimateAI	Benign	0.36	T
PROVEAN	Benign	-2.0	N;N;N;.
REVEL	Benign	0.17
Sift	Benign	0.14	T;T;T;.
Sift4G	Benign	0.13	T;T;T;T
Polyphen		0.99	.;.;D;D
Vest4		0.44
MutPred		0.48		.;.;Gain of loop (P = 0.0195);Gain of loop (P = 0.0195);
MVP		0.55
MPC		0.30
ClinPred		0.35	T
GERP RS		-0.19
Varity_R		0.34
gMVP		0.73

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

Publications

LitVar

Other links and lift over

dbSNP: rs551644836; hg19: chr11-58892859;