NM_001370485.4:c.-623+5885A>T
Variant summary
Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2BP4_Strong
The NM_001370485.4(OR7C1):c.-623+5885A>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.
Frequency
Consequence
NM_001370485.4 intron
Scores
Clinical Significance
Conservation
Publications
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ACMG classification
Our verdict: Likely_benign. The variant received -2 ACMG points.
Variant Effect in Transcripts
ACMG analysis was done for transcript: NM_001370485.4. You can select a different transcript below to see updated ACMG assignments.
RefSeq Transcripts
| Selected | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| OR7C1 | NM_001370485.4 | MANE Select | c.-623+5885A>T | intron | N/A | NP_001357414.2 | |||
| OR7A5 | NM_017506.2 | MANE Select | c.-13-935A>T | intron | N/A | NP_059976.1 | |||
| OR7A5 | NM_001370480.1 | c.-248-598A>T | intron | N/A | NP_001357409.1 |
Ensembl Transcripts
| Selected | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| OR7C1 | ENST00000641666.2 | MANE Select | c.-623+5885A>T | intron | N/A | ENSP00000493429.1 | |||
| OR7A5 | ENST00000322301.5 | TSL:6 MANE Select | c.-13-935A>T | intron | N/A | ENSP00000316955.3 | |||
| OR7C1 | ENST00000642000.1 | c.-202+5885A>T | intron | N/A | ENSP00000493248.1 |
Frequencies
GnomAD3 genomes Cov.: 32
GnomAD4 genome Cov.: 32
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at