NM_006612.6:c.1111G>A
Variant summary
Our verdict is Benign. Variant got -13 ACMG points: 0P and 13B. BP4_StrongBP6BS1BS2
The NM_006612.6(KIF1C):c.1111G>A(p.Ala371Thr) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00426 in 1,614,248 control chromosomes in the GnomAD database, including 20 homozygotes. In-silico tool predicts a benign outcome for this variant. 13/21 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Conflicting classifications of pathogenicity (no stars).
Frequency
Consequence
NM_006612.6 missense
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Benign. Variant got -13 ACMG points.
Transcripts
RefSeq
Ensembl
Frequencies
GnomAD3 genomes AF: 0.00355 AC: 541AN: 152250Hom.: 1 Cov.: 32
GnomAD3 exomes AF: 0.00337 AC: 847AN: 251406Hom.: 1 AF XY: 0.00327 AC XY: 444AN XY: 135882
GnomAD4 exome AF: 0.00434 AC: 6342AN: 1461880Hom.: 19 Cov.: 32 AF XY: 0.00428 AC XY: 3109AN XY: 727238
GnomAD4 genome AF: 0.00355 AC: 541AN: 152368Hom.: 1 Cov.: 32 AF XY: 0.00360 AC XY: 268AN XY: 74516
ClinVar
Submissions by phenotype
Hereditary spastic paraplegia Uncertain:1Benign:1
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not specified Benign:1
This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease. -
Spastic ataxia 2 Benign:1
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not provided Benign:1
KIF1C: BS2 -
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at