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Variant summary

Our verdict is Likely benign. Variant got -5 ACMG points: 0P and 5B. BP3 BS1

The NM_001388492.1(HTT):c.66_110dup(p.Gln24_Gln38dup) variant causes a inframe insertion change. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: 𝑓 0.00045 (0 hom., cov: 0)
  • Exomes 𝑓: 0.00019 (0 hom.)
  • Failed GnomAD Quality Control
• Consequence: HTT NM_001388492.1 inframe_insertion
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 4.84

Genes affected

HTT (HGNC:4851): (huntingtin) Huntingtin is a disease gene linked to Huntington's disease, a neurodegenerative disorder characterized by loss of striatal neurons. This is thought to be caused by an expanded, unstable trinucleotide repeat in the huntingtin gene, which translates as a polyglutamine repeat in the protein product. A fairly broad range of trinucleotide repeats (9-35) has been identified in normal controls, and repeat numbers in excess of 40 have been described as pathological. The huntingtin locus is large, spanning 180 kb and consisting of 67 exons. The huntingtin gene is widely expressed and is required for normal development. It is expressed as 2 alternatively polyadenylated forms displaying different relative abundance in various fetal and adult tissues. The larger transcript is approximately 13.7 kb and is expressed predominantly in adult and fetal brain whereas the smaller transcript of approximately 10.3 kb is more widely expressed. The genetic defect leading to Huntington's disease may not necessarily eliminate transcription, but may confer a new property on the mRNA or alter the function of the protein. One candidate is the huntingtin-associated protein-1, highly expressed in brain, which has increased affinity for huntingtin protein with expanded polyglutamine repeats. This gene contains an upstream open reading frame in the 5' UTR that inhibits expression of the huntingtin gene product through translational repression. [provided by RefSeq, Jul 2016]

ACMG classification

Verdict is Likely_benign. Variant got -5 ACMG points.

• BP3: Nonframeshift variant in repetitive region in NM_001388492.1
• BS1: Variant frequency is greater than expected in population nfe. gnomad4 allele frequency = 0.000447 (59/131884) while in subpopulation NFE AF= 0.000634 (39/61488). AF 95% confidence interval is 0.000476. There are 0 homozygotes in gnomad4. There are 26 alleles in male gnomad4 subpopulation. Median coverage is 0. This position pass quality control queck.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
HTT	NM_001388492.1	c.66_110dup	p.Gln24_Gln38dup	inframe_insertion	1/67	ENST00000355072.11
HTT	NM_002111.8	c.66_110dup	p.Gln24_Gln38dup	inframe_insertion	1/67

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
HTT	ENST00000355072.11	c.66_110dup	p.Gln24_Gln38dup	inframe_insertion	1/67	1	NM_001388492.1	P2

Frequencies

GnomAD3 genomes AF: 0.000448 AC: 59 AN: 131786 Hom.: 0 Cov.: 0

Gnomad AFR AF: 0.000339

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.000149

Gnomad ASJ AF: 0.00

Gnomad EAS AF: 0.000242

Gnomad SAS AF: 0.000511

Gnomad FIN AF: 0.000271

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.000634

Gnomad OTH AF: 0.000557

GnomAD4 exome Data not reliable, filtered out with message: AS_VQSR AF: 0.000191 AC: 234 AN: 1225836 Hom.: 0 Cov.: 0 AF XY: 0.000224 AC XY: 136 AN XY: 608138

Gnomad4 AFR exome AF: 0.000116

Gnomad4 AMR exome AF: 0.000165

Gnomad4 ASJ exome AF: 0.000308

Gnomad4 EAS exome AF: 0.000103

Gnomad4 SAS exome AF: 0.000208

Gnomad4 FIN exome AF: 0.000185

Gnomad4 NFE exome AF: 0.000192

Gnomad4 OTH exome AF: 0.000193

GnomAD4 genome AF: 0.000447 AC: 59 AN: 131884 Hom.: 0 Cov.: 0 AF XY: 0.000410 AC XY: 26 AN XY: 63426

Gnomad4 AFR AF: 0.000338

Gnomad4 AMR AF: 0.000149

Gnomad4 ASJ AF: 0.00

Gnomad4 EAS AF: 0.000242

Gnomad4 SAS AF: 0.000512

Gnomad4 FIN AF: 0.000271

Gnomad4 NFE AF: 0.000634

Gnomad4 OTH AF: 0.000551

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: rs71180116; hg19: chr4-3076603;