NM_018993.4:c.-36-2941_-36-2935dupTTTTTTT

Variant names:

• chr20-19886612-C-CTTTTTTT
• rs11362637
• NM_018993.4:c.-36-2941_-36-2935dupTTTTTTT

Variant summary

Our verdict is Likely benign. Variant got -4 ACMG points: 0P and 4B. BS1

The NM_018993.4(RIN2):​c.-36-2941_-36-2935dupTTTTTTT variant causes a intron change involving the alteration of a non-conserved nucleotide. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: 𝑓 0.000095 (0 hom., cov: 0)
  • Exomes 𝑓: 0.00037 (0 hom.)
• Consequence: RIN2 NM_018993.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.844

Genes affected

RIN2 (HGNC:18750): (Ras and Rab interactor 2) The RAB5 protein is a small GTPase involved in membrane trafficking in the early endocytic pathway. The protein encoded by this gene binds the GTP-bound form of the RAB5 protein preferentially over the GDP-bound form, and functions as a guanine nucleotide exchange factor for RAB5. The encoded protein is found primarily as a tetramer in the cytoplasm and does not bind other members of the RAB family. Mutations in this gene cause macrocephaly alopecia cutis laxa and scoliosis (MACS) syndrome, an elastic tissue disorder, as well as the related connective tissue disorder, RIN2 syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2011]

ACMG classification

Verdict is Likely_benign. Variant got -4 ACMG points.

• BS1: Variant frequency is greater than expected in population amr. gnomad4_exome allele frequency = 0.000367 (149/405646) while in subpopulation AMR AF= 0.000979 (16/16338). AF 95% confidence interval is 0.000614. There are 0 homozygotes in gnomad4_exome. There are 84 alleles in male gnomad4_exome subpopulation. Median coverage is 0. This position pass quality control queck.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
RIN2	NM_018993.4	c.-36-2941_-36-2935dupTTTTTTT		intron_variant	Intron 2 of 12	ENST00000255006.12	NP_061866.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
RIN2	ENST00000255006.12	c.-36-2941_-36-2935dupTTTTTTT		intron_variant	Intron 2 of 12	2	NM_018993.4	ENSP00000255006.7
RIN2	ENST00000648440	c.-192_-186dupTTTTTTT		5_prime_UTR_variant	Exon 1 of 12			ENSP00000498085.1
RIN2	ENST00000432334.2	n.537-2941_537-2935dupTTTTTTT		intron_variant	Intron 3 of 3	4
RIN2	ENST00000648165.1	n.618-2941_618-2935dupTTTTTTT		intron_variant	Intron 3 of 3

Frequencies

GnomAD3 genomes AF: 0.0000954 AC: 11 AN: 115262 Hom.: 0 Cov.: 0

Gnomad AFR AF: 0.0000681

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.0000918

Gnomad ASJ AF: 0.000332

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.00

Gnomad FIN AF: 0.00

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.000122

Gnomad OTH AF: 0.00

GnomAD4 exome AF: 0.000367 AC: 149 AN: 405646 Hom.: 0 Cov.: 0 AF XY: 0.000383 AC XY: 84 AN XY: 219178

Gnomad4 AFR exome AF: 0.000820

Gnomad4 AMR exome AF: 0.000979

Gnomad4 ASJ exome AF: 0.000309

Gnomad4 EAS exome AF: 0.000698

Gnomad4 SAS exome AF: 0.000719

Gnomad4 FIN exome AF: 0.0000914

Gnomad4 NFE exome AF: 0.000276

Gnomad4 OTH exome AF: 0.000233

GnomAD4 genome AF: 0.0000954 AC: 11 AN: 115262 Hom.: 0 Cov.: 0 AF XY: 0.0000369 AC XY: 2 AN XY: 54182

Gnomad4 AFR AF: 0.0000681

Gnomad4 AMR AF: 0.0000918

Gnomad4 ASJ AF: 0.000332

Gnomad4 EAS AF: 0.00

Gnomad4 SAS AF: 0.00

Gnomad4 FIN AF: 0.00

Gnomad4 NFE AF: 0.000122

Gnomad4 OTH AF: 0.00

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs11362637; hg19: chr20-19867256;