rs1398842143

Variant names:

• chr10-121565665-T-A
• rs1398842143
• NM_000141.5:c.149A>T

Your query was ambiguous. Multiple possible variants found:

• chr10-121565665-T-A
• chr10-121565665-T-C
• chr10-121565665-T-G

Variant summary

Our verdict is Uncertain significance. Variant got 1 ACMG points: 3P and 2B. PM2 PP2 BP4_Moderate

The NM_000141.5(FGFR2):​c.149A>T​(p.Tyr50Phe) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000000684 in 1,461,894 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. 14/21 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)
  • Exomes 𝑓: 6.8e-7 (0 hom.)
• Consequence: FGFR2 NM_000141.5 missense
• Clinical Significance: Uncertain significance criteria provided, multiple submitters, no conflicts U:3
• Conservation: PhyloP100: 2.68

Genes affected

FGFR2 (HGNC:3689): (fibroblast growth factor receptor 2) The protein encoded by this gene is a member of the fibroblast growth factor receptor family, where amino acid sequence is highly conserved between members and throughout evolution. FGFR family members differ from one another in their ligand affinities and tissue distribution. A full-length representative protein consists of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain. The extracellular portion of the protein interacts with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation. This particular family member is a high-affinity receptor for acidic, basic and/or keratinocyte growth factor, depending on the isoform. Mutations in this gene are associated with Crouzon syndrome, Pfeiffer syndrome, Craniosynostosis, Apert syndrome, Jackson-Weiss syndrome, Beare-Stevenson cutis gyrata syndrome, Saethre-Chotzen syndrome, and syndromic craniosynostosis. Multiple alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jan 2009]

ACMG classification

Verdict is Uncertain_significance. Variant got 1 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• PP2: Missense variant in the FGFR2 gene, where missense mutations are typically associated with disease (based on misZ statistic). The gene has 114 curated pathogenic missense variants (we use a threshold of 10). The gene has 24 curated benign missense variants. Gene score misZ: 2.402 (below the threshold of 3.09). Trascript score misZ: 4.4365 (above the threshold of 3.09). GenCC associations: The gene is linked to Pfeiffer syndrome type 3, Antley-Bixler syndrome, Pfeiffer syndrome type 2, Saethre-Chotzen syndrome, Beare-Stevenson cutis gyrata syndrome, Crouzon syndrome, Jackson-Weiss syndrome, Pfeiffer syndrome type 1, LADD syndrome 1, Pfeiffer syndrome, bent bone dysplasia syndrome 1, Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis, familial scaphocephaly syndrome, McGillivray type, Apert syndrome, LADD syndrome.
• BP4: Computational evidence support a benign effect (MetaRNN=0.14112154).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
FGFR2	NM_000141.5	c.149A>T	p.Tyr50Phe	missense_variant	Exon 3 of 18	ENST00000358487.10	NP_000132.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
FGFR2	ENST00000358487.10	c.149A>T	p.Tyr50Phe	missense_variant	Exon 3 of 18	1	NM_000141.5	ENSP00000351276.6
FGFR2	ENST00000457416.7	c.149A>T	p.Tyr50Phe	missense_variant	Exon 3 of 18	1		ENSP00000410294.2
FGFR2	ENST00000369056.5	c.149A>T	p.Tyr50Phe	missense_variant	Exon 2 of 17	1		ENSP00000358052.1
FGFR2	ENST00000369058.7	c.149A>T	p.Tyr50Phe	missense_variant	Exon 3 of 17	1		ENSP00000358054.3
FGFR2	ENST00000369061.8	c.149A>T	p.Tyr50Phe	missense_variant	Exon 2 of 15	1		ENSP00000358057.4
FGFR2	ENST00000613048.4	c.110-1086A>T		intron_variant	Intron 2 of 16	5		ENSP00000484154.1
FGFR2	ENST00000369059.5	c.110-14206A>T		intron_variant	Intron 2 of 15	5		ENSP00000358055.1
FGFR2	ENST00000360144.7	c.110-1086A>T		intron_variant	Intron 2 of 16	2		ENSP00000353262.3
FGFR2	ENST00000604236.5	n.110-14206A>T		intron_variant	Intron 2 of 16	1		ENSP00000474109.1

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome AF: 6.84e-7 AC: 1 AN: 1461894 Hom.: 0 Cov.: 31 AF XY: 0.00000138 AC XY: 1 AN XY: 727248

Gnomad4 AFR exome AF: 0.00

Gnomad4 AMR exome AF: 0.00

Gnomad4 ASJ exome AF: 0.00

Gnomad4 EAS exome AF: 0.00

Gnomad4 SAS exome AF: 0.00

Gnomad4 FIN exome AF: 0.00

Gnomad4 NFE exome AF: 8.99e-7

Gnomad4 OTH exome AF: 0.00

GnomAD4 genome Cov.: 32

Bravo AF: 0.00000378

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:3

Revision: criteria provided, multiple submitters, no conflicts

Submissions by phenotype

not provided Uncertain:2

Sep 27, 2017

Geisinger Autism and Developmental Medicine Institute, Geisinger Health System

Significance: Uncertain significance

Review Status: criteria provided, single submitter

Collection Method: clinical testing;provider interpretation

This 6 year old male with borderline to mild intellectual disability, hyperkinesis, disruptive behavior, esophageal atresia, duodenal atresia, TE fistula, atrial septal defect, left superior vena cava, slightly shortened and mildly upslanting palpebral, mild right posterior plagiocephaly, and right esotropia was found to carry a maternally inherited missense variant in FGFR2. The variant is absent from population databases. It is a non-conservative substitution but occurs at a position that is not conserved across species. -

Aug 15, 2019

GeneDx

Significance: Uncertain significance

Review Status: criteria provided, single submitter

Collection Method: clinical testing

Not observed in large population cohorts (Lek et al., 2016); In silico analysis, which includes protein predictors and evolutionary conservation, supports that this variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge -

FGFR2-related craniosynostosis Uncertain:1

Aug 28, 2021

Labcorp Genetics (formerly Invitae), Labcorp

Significance: Uncertain significance

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.060
BayesDel_addAF	Benign	-0.17	T
BayesDel_noAF	Benign	-0.48
CADD	Benign	16
DANN	Benign	0.87
DEOGEN2	Benign	0.36	.;T;.;.;T;.;.;.;.
Eigen	Benign	-0.33
Eigen_PC	Benign	-0.19
FATHMM_MKL	Uncertain	0.92	D
LIST_S2	Uncertain	0.88	D;T;T;T;T;T;T;T;D
M_CAP	Benign	0.0046	T
MetaRNN	Benign	0.14	T;T;T;T;T;T;T;T;T
MetaSVM	Benign	-1.1	T
MutationAssessor	Benign	0.88	L;L;L;L;.;L;L;L;L
PrimateAI	Uncertain	0.50	T
PROVEAN	Benign	-0.32	N;N;N;N;N;N;N;N;N
REVEL	Benign	0.060
Sift	Benign	0.059	T;T;T;T;T;T;T;T;T
Sift4G	Benign	0.63	T;T;T;T;T;T;T;T;T
Polyphen		0.0	.;B;.;.;.;.;B;.;.
Vest4		0.29
MutPred		0.53		Loss of phosphorylation at Y50 (P = 0.0205);Loss of phosphorylation at Y50 (P = 0.0205);Loss of phosphorylation at Y50 (P = 0.0205);Loss of phosphorylation at Y50 (P = 0.0205);Loss of phosphorylation at Y50 (P = 0.0205);Loss of phosphorylation at Y50 (P = 0.0205);Loss of phosphorylation at Y50 (P = 0.0205);Loss of phosphorylation at Y50 (P = 0.0205);Loss of phosphorylation at Y50 (P = 0.0205);
MVP		0.35
MPC		0.25
ClinPred		0.17	T
GERP RS		2.9
Varity_R		0.088
gMVP		0.23

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.040		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: rs1398842143; hg19: chr10-123325179; COSMIC: COSV60640757;