rs56300365

Variant names:

• chr19-18753562-A-C
• rs56300365
• NM_015321.3:c.601A>C

Your query was ambiguous. Multiple possible variants found:

• chr19-18753562-A-C
• chr19-18753562-A-G

Variant summary

Our verdict is Uncertain significance. The variant received 1 ACMG points: 2P and 1B. PM2 BP4

The NM_015321.3(CRTC1):​c.601A>C​(p.Lys201Gln) variant causes a missense change. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. K201E) has been classified as Uncertain significance.

• Frequency: Genomes: not found (cov: 31)
• Consequence: CRTC1 NM_015321.3 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 3.69
• Publications: 1 publications found

Genes affected

CRTC1 (HGNC:16062): (CREB regulated transcription coactivator 1) Enables cAMP response element binding protein binding activity. Involved in positive regulation of transcription by RNA polymerase II. Located in cytosol; nuclear body; and plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Uncertain_significance. The variant received 1 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.3061605).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CRTC1	NM_015321.3	c.601A>C	p.Lys201Gln	missense_variant	Exon 6 of 14	ENST00000321949.13	NP_056136.2
CRTC1	NM_001098482.2	c.649A>C	p.Lys217Gln	missense_variant	Exon 7 of 15		NP_001091952.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CRTC1	ENST00000321949.13	c.601A>C	p.Lys201Gln	missense_variant	Exon 6 of 14	1	NM_015321.3	ENSP00000323332.7
CRTC1	ENST00000338797.10	c.649A>C	p.Lys217Gln	missense_variant	Exon 7 of 15	1		ENSP00000345001.5
CRTC1	ENST00000594658.5	c.478A>C	p.Lys160Gln	missense_variant	Exon 6 of 14	1		ENSP00000468893.1
CRTC1	ENST00000601916.1	c.376A>C	p.Lys126Gln	missense_variant	Exon 5 of 10	5		ENSP00000469285.1

Frequencies

GnomAD3 genomes Cov.: 31

GnomAD4 exome Cov.: 30

GnomAD4 genome Cov.: 31

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.13
BayesDel_addAF	Benign	-0.085	T
BayesDel_noAF	Benign	-0.36
CADD	Uncertain	25
DANN	Uncertain	0.99
DEOGEN2	Uncertain	0.54	D;.;.;.
Eigen	Uncertain	0.35
Eigen_PC	Uncertain	0.38
FATHMM_MKL	Pathogenic	0.99	D
LIST_S2	Uncertain	0.91	D;D;D;D
M_CAP	Benign	0.031	D
MetaRNN	Benign	0.31	T;T;T;T
MetaSVM	Benign	-0.79	T
MutationAssessor	Uncertain	2.2	M;.;.;.
PhyloP100		3.7
PrimateAI	Uncertain	0.49	T
PROVEAN	Uncertain	-2.9	D;D;.;.
REVEL	Benign	0.075
Sift	Benign	0.063	T;T;.;.
Sift4G	Benign	0.075	T;T;T;T
Polyphen		0.88	P;P;.;.
Vest4		0.45
MutPred		0.24		Loss of methylation at K201 (P = 0.0025);.;.;.;
MVP		0.63
MPC		1.4
ClinPred		0.98	D
GERP RS		4.7
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.7
Varity_R		0.29
gMVP		0.30
Mutation Taster		=71/29	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: rs56300365; hg19: chr19-18864372;