chr6-118672479-C-G

Variant names:

• chr6-118672479-C-G
• rs11756440
• ENST00000434604.5:c.-27-19671G>C

Variant summary

Our verdict is Likely benign. Variant got -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_001178035.2(CEP85L):​c.-27-19671G>C variant causes a intron 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. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 33)
• Consequence: CEP85L NM_001178035.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.42

Genes affected

CEP85L (HGNC:21638): (centrosomal protein 85 like) The protein encoded by this gene was identified as a breast cancer antigen. Nothing more is known of its function at this time. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]

LOC124901388 (HGNC:):

ACMG classification

Verdict is Likely_benign. Variant got -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.99).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CEP85L	NM_001178035.2	c.-27-19671G>C		intron_variant	Intron 1 of 13		NP_001171506.1
CEP85L	XM_017010846.2	c.-138-7958G>C		intron_variant	Intron 1 of 14		XP_016866335.1
CEP85L	XM_047418758.1	c.-27-19671G>C		intron_variant	Intron 2 of 14		XP_047274714.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CEP85L	ENST00000434604.5	c.-27-19671G>C		intron_variant	Intron 1 of 8	1		ENSP00000392131.1
CEP85L	ENST00000392500.7	c.-138-7958G>C		intron_variant	Intron 1 of 7	1		ENSP00000376288.3
CEP85L	ENST00000368488.9	c.-27-19671G>C		intron_variant	Intron 1 of 13	5		ENSP00000357474.5

Frequencies

GnomAD3 genomes Cov.: 33

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome Cov.: 33

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.99
CADD	Benign	0.37
DANN	Benign	0.39

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs11756440; hg19: chr6-118993642;