rs78670873

Variant names:

• chr11-6270078-C-A
• rs78670873
• NM_176875.4:c.404-10C>A

Your query was ambiguous. Multiple possible variants found:

• chr11-6270078-C-A
• chr11-6270078-C-G
• chr11-6270078-C-T

Variant summary

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

The NM_176875.4(CCKBR):​c.404-10C>A 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: 32)
• Consequence: CCKBR NM_176875.4 intron
• Scores: Splicing: ADA: 0.001662
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.110

Genes affected

CCKBR (HGNC:1571): (cholecystokinin B receptor) This gene encodes a G-protein coupled receptor for gastrin and cholecystokinin (CCK), regulatory peptides of the brain and gastrointestinal tract. This protein is a type B gastrin receptor, which has a high affinity for both sulfated and nonsulfated CCK analogs and is found principally in the central nervous system and the gastrointestinal tract. Alternative splicing results in multiple transcript variants. A misspliced transcript variant including an intron has been observed in cells from colorectal and pancreatic tumors. [provided by RefSeq, Dec 2015]

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=-0.66).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CCKBR	NM_176875.4	c.404-10C>A		intron_variant	Intron 2 of 4	ENST00000334619.7	NP_795344.1
CCKBR	NM_001363552.2	c.404-10C>A		intron_variant	Intron 2 of 3		NP_001350481.1
CCKBR	NM_001318029.2	c.152-10C>A		intron_variant	Intron 1 of 3		NP_001304958.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CCKBR	ENST00000334619.7	c.404-10C>A		intron_variant	Intron 2 of 4	1	NM_176875.4	ENSP00000335544.2
CCKBR	ENST00000525462.1	c.404-10C>A		intron_variant	Intron 2 of 3	1		ENSP00000435534.1
CCKBR	ENST00000525014.1	c.*150C>A		3_prime_UTR_variant	Exon 2 of 2	4		ENSP00000437001.1
CCKBR	ENST00000532715.5	c.152-10C>A		intron_variant	Intron 1 of 3	3		ENSP00000432079.1

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 33

GnomAD4 genome Cov.: 32

Bravo AF: 0.00000756

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.66
CADD	Benign	7.6
DANN	Benign	0.68

Splicing

Name	Calibrated prediction	Score	Prediction
dbscSNV1_ADA	Benign	0.0017
dbscSNV1_RF	Benign	0.28
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: rs78670873; hg19: chr11-6291308;