rs201701235

Variant names:

• chrX-155511709-C-G
• rs201701235
• NM_018196.4:c.722G>C

Your query was ambiguous. Multiple possible variants found:

• chrX-155511709-C-G
• chrX-155511709-C-T

Variant summary

Our verdict is Uncertain significance. Variant got 3 ACMG points: 3P and 0B. PM2 PP3

The NM_018196.4(TMLHE):​c.722G>C​(p.Arg241Pro) variant causes a missense change. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a pathogenic outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 22)
• Consequence: TMLHE NM_018196.4 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 4.11

Genes affected

TMLHE (HGNC:18308): (trimethyllysine hydroxylase, epsilon) This gene encodes the protein trimethyllysine dioxygenase which is the first enzyme in the carnitine biosynthesis pathway. Carnitine play an essential role in the transport of activated fatty acids across the inner mitochondrial membrane. The encoded protein converts trimethyllysine into hydroxytrimethyllysine. A pseudogene of this gene is found on chromosome X. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2010]

TMLHE-AS1 (HGNC:44261): (TMLHE antisense RNA 1)

ACMG classification

Verdict is Uncertain_significance. Variant got 3 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• PP3: MetaRNN computational evidence supports a deleterious effect, 0.829

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
TMLHE	NM_018196.4	c.722G>C	p.Arg241Pro	missense_variant	Exon 5 of 8	ENST00000334398.8	NP_060666.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
TMLHE	ENST00000334398.8	c.722G>C	p.Arg241Pro	missense_variant	Exon 5 of 8	1	NM_018196.4	ENSP00000335261.3
TMLHE	ENST00000369439.4	c.722G>C	p.Arg241Pro	missense_variant	Exon 5 of 7	1		ENSP00000358447.4
TMLHE	ENST00000675642.1	c.755G>C	p.Arg252Pro	missense_variant	Exon 6 of 9			ENSP00000502604.1
TMLHE-AS1	ENST00000452506.1	n.67+22320C>G		intron_variant	Intron 1 of 1	5

Frequencies

GnomAD3 genomes Cov.: 22

GnomAD4 exome Cov.: 29

GnomAD4 genome Cov.: 22

Bravo AF: 0.00000756

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Pathogenic	0.84
BayesDel_addAF	Uncertain	0.16	D
BayesDel_noAF	Uncertain	-0.010
CADD	Uncertain	24
DANN	Uncertain	0.99
DEOGEN2	Benign	0.11	T;.
FATHMM_MKL	Uncertain	0.90	D
LIST_S2	Uncertain	0.92	D;D
M_CAP	Benign	0.075	D
MetaRNN	Pathogenic	0.83	D;D
MetaSVM	Benign	-0.45	T
MutationAssessor	Benign	0.27	N;N
PrimateAI	Pathogenic	0.83	D
PROVEAN	Benign	-0.63	N;N
REVEL	Uncertain	0.56
Sift	Benign	0.18	T;T
Sift4G	Benign	0.24	T;T
Polyphen		1.0	D;D
Vest4		0.81
MutPred		0.68		Gain of ubiquitination at K236 (P = 0.0756);Gain of ubiquitination at K236 (P = 0.0756);
MVP		0.78
MPC		0.39
ClinPred		0.68	D
GERP RS		2.8
Varity_R		0.28
gMVP		0.88

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: rs201701235; hg19: chrX-154741370;