10-14867895-A-G
Variant summary
Our verdict is Benign. Variant got -8 ACMG points: 0P and 8B. BP4_StrongBS2
The NM_016299.4(HSPA14):c.1366A>G(p.Thr456Ala) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000868 in 1,613,278 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. 14/21 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).
Frequency
Consequence
NM_016299.4 missense
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Benign. Variant got -8 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
HSPA14 | NM_016299.4 | c.1366A>G | p.Thr456Ala | missense_variant | 12/14 | ENST00000378372.8 | |
LOC124902382 | XR_007062064.1 | n.229-15T>C | splice_polypyrimidine_tract_variant, intron_variant, non_coding_transcript_variant | ||||
LOC124902382 | XR_007062065.1 | n.229-15T>C | splice_polypyrimidine_tract_variant, intron_variant, non_coding_transcript_variant | ||||
LOC124902382 | XR_007062066.1 | n.229-15T>C | splice_polypyrimidine_tract_variant, intron_variant, non_coding_transcript_variant |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
HSPA14 | ENST00000378372.8 | c.1366A>G | p.Thr456Ala | missense_variant | 12/14 | 1 | NM_016299.4 | P1 |
Frequencies
GnomAD3 genomes ? AF: 0.0000131 AC: 2AN: 152198Hom.: 0 Cov.: 32
GnomAD3 exomes AF: 0.0000240 AC: 6AN: 250226Hom.: 0 AF XY: 0.0000222 AC XY: 3AN XY: 135254
GnomAD4 exome AF: 0.00000821 AC: 12AN: 1461080Hom.: 0 Cov.: 31 AF XY: 0.00000413 AC XY: 3AN XY: 726840
GnomAD4 genome ? AF: 0.0000131 AC: 2AN: 152198Hom.: 0 Cov.: 32 AF XY: 0.0000134 AC XY: 1AN XY: 74372
ClinVar
Submissions by phenotype
not specified Uncertain:1
Uncertain significance, criteria provided, single submitter | clinical testing | Ambry Genetics | May 31, 2023 | The c.1366A>G (p.T456A) alteration is located in exon 12 (coding exon 12) of the HSPA14 gene. This alteration results from a A to G substitution at nucleotide position 1366, causing the threonine (T) at amino acid position 456 to be replaced by an alanine (A). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. - |
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at