rs1144713

Variant names:

• chr12-32108305-A-C
• rs1144713
• NM_001714.4:c.213+761A>C

Your query was ambiguous. Multiple possible variants found:

• chr12-32108305-A-C
• chr12-32108305-A-G
• chr12-32108305-A-T

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_001413182.1(BICD1):​c.*617A>C variant causes a 3 prime UTR 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)
  • Exomes 𝑓: 0.0 (0 hom.)
  • Failed GnomAD Quality Control
• Consequence: BICD1 NM_001413182.1 3_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.797
• Publications: 13 publications found

Genes affected

BICD1 (HGNC:1049): (BICD cargo adaptor 1) This gene encodes an adaptor protein that belongs to the bicaudal D family of dynein cargo adaptors. The encoded protein acts as an intracellular cargo transport cofactor that regulates the microtubule-based loading of cargo onto the dynein motor complex. It also controls dynein motor activity and coordination. It has a domain architecture consisting of coiled-coil domains at the N- and C-termini that are highly conserved in other family members. Naturally occurring mutations in this gene are associated with short telomere length and emphysema. [provided by RefSeq, Aug 2017]

ACMG classification

Our verdict: Likely_benign. The variant received -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001413182.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	BICD1	NM_001714.4	MANE Select	c.213+761A>C		intron	N/A	NP_001705.2
	BICD1	NM_001413182.1		c.*617A>C		3_prime_UTR	Exon 2 of 2	NP_001400111.1
	BICD1	NM_001413183.1		c.*394A>C		3_prime_UTR	Exon 2 of 2	NP_001400112.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	BICD1	ENST00000652176.1	MANE Select	c.213+761A>C		intron	N/A	ENSP00000498700.1
	BICD1	ENST00000548411.6	TSL:1	c.213+761A>C		intron	N/A	ENSP00000446793.1
	BICD1	ENST00000395758.3	TSL:1	n.213+761A>C		intron	N/A	ENSP00000379107.3

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Data not reliable, filtered out with message: AC0 AF: 0.00 AC: 0 AN: 43350 Hom.: 0 Cov.: 0 AF XY: 0.00 AC XY: 0 AN XY: 22102

African (AFR) AF: 0.00 AC: 0 AN: 1198

American (AMR) AF: 0.00 AC: 0 AN: 3340

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 1262

East Asian (EAS) AF: 0.00 AC: 0 AN: 2810

South Asian (SAS) AF: 0.00 AC: 0 AN: 3856

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 1464

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 144

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 26762

Other (OTH) AF: 0.00 AC: 0 AN: 2514

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	9.7
DANN	Benign	0.84
PhyloP100		0.80

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: rs1144713; hg19: chr12-32261239;