5-80654344-C-CTGGCGCGTCTCGCCCAGGT

Variant names:

• chr5-80654344-C-CTGGCGCGTCTCGCCCAGGT
• rs70991108
• NM_000791.4:c.86+59_86+60insACCTGGGCGAGACGCGCCA

Variant summary

Our verdict is Uncertain significance. The variant received 0 ACMG points: 0P and 0B.

The NM_000791.4(DHFR):​c.86+59_86+60insACCTGGGCGAGACGCGCCA variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000141 in 1,416,272 control chromosomes in the GnomAD database, with no homozygous occurrence. It is difficult to determine the true allele frequency of this variant because it is of type INS_BIG, and the frequency of such variant types in population databases may be underestimated and unreliable. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: not found (cov: 0)
  • Exomes 𝑓: 0.0000014 (0 hom.)
• Consequence: DHFR NM_000791.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.762
• Publications: 0 publications found

Genes affected

DHFR (HGNC:2861): (dihydrofolate reductase) Dihydrofolate reductase converts dihydrofolate into tetrahydrofolate, a methyl group shuttle required for the de novo synthesis of purines, thymidylic acid, and certain amino acids. While the functional dihydrofolate reductase gene has been mapped to chromosome 5, multiple intronless processed pseudogenes or dihydrofolate reductase-like genes have been identified on separate chromosomes. Dihydrofolate reductase deficiency has been linked to megaloblastic anemia. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2014]

DHFR Gene-Disease associations (from GenCC):

• constitutional megaloblastic anemia with severe neurologic disease

  Inheritance: AR Classification: DEFINITIVE, STRONG, MODERATE Submitted by: Labcorp Genetics (formerly Invitae), G2P, Ambry Genetics

ACMG classification

Our verdict: Uncertain_significance. The variant received 0 ACMG points.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
DHFR	NM_000791.4	c.86+59_86+60insACCTGGGCGAGACGCGCCA		intron_variant	Intron 1 of 5	ENST00000439211.7	NP_000782.1
DHFR	NM_001290354.2	c.-21+59_-21+60insACCTGGGCGAGACGCGCCA		intron_variant	Intron 1 of 4		NP_001277283.1
DHFR	NM_001290357.2	c.86+59_86+60insACCTGGGCGAGACGCGCCA		intron_variant	Intron 1 of 4		NP_001277286.1
DHFR	NR_110936.2	n.580+59_580+60insACCTGGGCGAGACGCGCCA		intron_variant	Intron 1 of 3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
DHFR	ENST00000439211.7	c.86+59_86+60insACCTGGGCGAGACGCGCCA		intron_variant	Intron 1 of 5	1	NM_000791.4	ENSP00000396308.2

Frequencies

GnomAD3 genomes Cov.: 0

GnomAD4 exome AF: 0.00000141 AC: 2 AN: 1416272 Hom.: 0 AF XY: 0.00000142 AC XY: 1 AN XY: 705630

African (AFR) AF: 0.00 AC: 0 AN: 32588

American (AMR) AF: 0.00 AC: 0 AN: 44012

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 25654

East Asian (EAS) AF: 0.00 AC: 0 AN: 39414

South Asian (SAS) AF: 0.00 AC: 0 AN: 84782

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 52022

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 4102

European-Non Finnish (NFE) AF: 0.00000186 AC: 2 AN: 1075020

Other (OTH) AF: 0.00 AC: 0 AN: 58678

GnomAD4 genome Cov.: 0

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
PhyloP100		-0.76

Splicing

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

Other links and lift over

dbSNP: rs70991108; hg19: chr5-79950163;