87094235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 34033367-G-A

87094235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 34033367-G-T

87094618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 34033004-C-G

87094650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 34032972-G-A

87094650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 34032972-G-C

http://identifiers.org/hco/10/GRCh38#87094666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#34032956-C-A

87094666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 34032956-C-T

87095012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, undefined
orthologous variants: 34032611-G-A

87095012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, undefined
orthologous variants: 34032611-G-C

87095012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, undefined
orthologous variants: 34032611-G-T

87095067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron variant
orthologous variants: 34032555-G-T

87095077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron variant
orthologous variants: 34032545-G-A

87095077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron variant
orthologous variants: 34032545-G-C

87095117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron variant
orthologous variants: 34032533-G-A

87095117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron variant
orthologous variants: 34032533-G-T

http://identifiers.org/hco/10/GRCh38#87095204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#34032478-C-A

87095204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 34032478-C-T

87095207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 34032475-G-T

87095531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34032257-G-C

87095722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34032109-C-T

87095821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34032056-T-G

87096707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34031370-C-T

87096737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34031343-T-C

87096748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34031333-A-G

87096782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34031301-A-G

http://identifiers.org/hco/10/GRCh38#87096783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#34031300-A-C

87096783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34031300-A-T

87096902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34031082-G-A

http://identifiers.org/hco/10/GRCh38#87096952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#34031031-C-A

http://identifiers.org/hco/10/GRCh38#87096959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#34031024-C-A

87096959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34031024-C-G

87097199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34030710-A-T

87097316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34030648-T-G

87097332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34030632-G-A

87097342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34030617-C-G

87097353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34030591-G-T

87097358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34030586-C-T

87099091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34029528-A-G

87099185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34029428-A-G

87099319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34029289-T-C

http://identifiers.org/hco/10/GRCh38#87099692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#34028830-A-C

87099762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34028762-G-A

87099824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34028711-T-C

http://identifiers.org/hco/10/GRCh38#87105307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#34025135-A-C

87105410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34025040-A-G

87105442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34025004-A-G

http://identifiers.org/hco/10/GRCh38#87105464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#34024983-C-A

87105472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34024976-G-A

87105617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34024819-T-C

87105938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34024447-T-G

87105943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34024417-T-C

87105944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34024416-C-T

87105959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34024401-A-G

87105959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34024401-A-T

87106057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34024261-G-A

http://identifiers.org/hco/10/GRCh38#87106151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#34024182-C-A

87106151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34024182-C-T

87106206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34024133-T-C

http://identifiers.org/hco/10/GRCh38#87106227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#34024112-A-C

87106227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34024112-A-G

87106455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34023839-T-C

87106528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34023768-A-G

87106754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34023575-G-A

87106764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34023568-A-G

87106764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34023568-A-T

87106898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34023431-G-A

87114183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34023159-T-C

87118028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34018582-A-G

87118372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34018281-A-G

87118953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34016907-A-G

87119227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34015835-A-G

87119297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34015767-A-G

87119403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34015658-C-T

87119487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34015577-C-T

87120178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34015119-A-G

87126828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34013127-G-T

87126834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34013122-G-A

87127088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34012872-C-G

87133338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34011003-T-C

87133347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34010996-C-T

87133404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34010939-T-C

87134721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34009103-C-T

87134746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34009098-C-G

http://identifiers.org/hco/10/GRCh38#87134750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#34009095-C-A

87134851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34009009-A-G

87135096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34008799-G-C

87145481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33997696-C-T

87145542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33997639-G-A

87145562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33997609-G-A

87145572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33997599-A-G

87145627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33997540-T-C

87145934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33997235-A-G

87145934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33997235-A-T

87145996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33997172-G-A

87147562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33996210-G-A

87147657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33996109-A-G

87147742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33996052-T-G

87147766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33996028-G-A

87148260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33995825-G-A

87148315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33995790-G-C

http://identifiers.org/hco/10/GRCh38#87148348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#33995754-C-A

87148348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33995754-C-T

87148802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33995493-C-G

http://identifiers.org/hco/10/GRCh38#87149315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#33995347-A-C

87149315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33995347-A-G

87151105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33991099-G-A

87151219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33991005-A-G

87151360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33990897-T-G

87151379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33990878-A-G

87151384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 33990873-T-C

87151511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33990746-G-A

87151581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33990670-A-G

87151588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 33990663-A-G

87151643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33990608-T-C

87151666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 33990585-C-T

87151667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33990584-C-G

87151700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33990563-A-T

87151825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 33990441-T-C

http://identifiers.org/hco/10/GRCh38#87152025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#33990265-C-A

87152025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33990265-C-T

87152064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33990226-C-T

87152105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33990185-G-A

87152156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33990134-G-A

87152357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 33989933-G-T

87152375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33989918-G-C

87152375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 33989918-G-T

87152385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33989908-G-A

87152395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 33989898-T-C

87152470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33989865-C-G

87152470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 33989865-C-T

87152493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33989842-G-A

87152516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 33989819-C-T

87152570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33989765-T-C

87152587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 33989748-T-G

87152702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33989633-T-G

87152714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33989621-G-A

http://identifiers.org/hco/10/GRCh38#87153009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#33989358-C-A

87154379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33988983-T-C

87154403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33988959-G-A

87154403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33988959-G-T

87154477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33988893-T-A

87154492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33988879-T-C

87154527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33988845-T-C

http://identifiers.org/hco/10/GRCh38#87154611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#33988778-C-A

87154611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33988778-C-G

87155409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33988193-G-A

87155545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33988061-G-A

87155648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33987875-A-T

87155753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33987749-A-G

87155889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33987612-A-G

87156394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33987148-A-G

87156480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33987085-A-T

87157607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33985969-G-C

87157685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33985895-C-T

87158198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33981265-T-C

87169630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33974396-C-G

87169993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33973668-G-A

87170010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33973649-G-A

87170076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33973571-G-A

87170363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33973339-T-A

http://identifiers.org/hco/10/GRCh38#87170622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#33971182-A-C

http://identifiers.org/hco/10/GRCh38#87170677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#33971127-A-C

87170816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33970997-A-G

87170882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 33970931-T-C

87171321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33970050-G-C

87171339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33970026-A-G

87171702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 33969668-T-C

87171714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 33969654-C-T

http://identifiers.org/hco/10/GRCh38#87171721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#33969647-C-A

http://identifiers.org/hco/10/GRCh38#87172012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#33969386-A-C

87172069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33969330-C-G

87172270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33969131-A-G

http://identifiers.org/hco/10/GRCh38#87175530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#33967663-A-C

87175671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33967567-G-A

http://identifiers.org/hco/10/GRCh38#87175709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#33967547-A-C

87175709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33967547-A-G

87175741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33967512-T-A

87175741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33967512-T-C

87175996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33967216-G-A

87177449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33965069-A-G

87177486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33965038-G-A

87177497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33965027-G-A

87177554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33964968-G-A

87179092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33963882-C-G

87180011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33963535-G-C

87180162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33963383-T-C

87180347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33963189-T-C

87180351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33963185-T-C

87180421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33963112-A-G

87180436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33963096-G-A

87180436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33963096-G-C

87180436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33963096-G-T

87180672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33962891-T-C

87180672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33962891-T-G

http://identifiers.org/hco/10/GRCh38#87187086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#33960907-C-A

87187086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 33960907-C-T

http://identifiers.org/hco/10/GRCh38#87187218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#33960777-C-A

87187218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33960777-C-T

87187223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33960772-A-G

87187224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33960771-G-C

87187224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33960771-G-T

87187225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33960770-A-T

87187256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33960740-A-G

87187257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33960739-T-G

87187507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33960493-T-C

http://identifiers.org/hco/10/GRCh38#87190388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#33959634-C-A

87190505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33959520-A-G

87190580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33959445-G-A

http://identifiers.org/hco/10/GRCh38#87190897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28773
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#33958927-C-A