54874984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28790438-C-T

54874987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28790435-T-C

54874994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28790428-T-C

http://identifiers.org/hco/3/GRCh38#54875099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28790333-C-A

54875099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28790333-C-G

54875155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28790286-A-G

http://identifiers.org/hco/3/GRCh38#54875199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28790234-A-C

54875199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28790234-A-G

http://identifiers.org/hco/3/GRCh38#54875255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28790199-C-A

54875292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28790174-A-G

http://identifiers.org/hco/3/GRCh38#54875308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28790156-C-A

54875308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28790156-C-T

54875413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28790055-T-A

54875445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28790023-G-T

54875617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28789866-A-G

54875774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28789752-G-T

54875793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28789739-T-C

http://identifiers.org/hco/3/GRCh38#54875993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28789563-A-C

54875993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28789563-A-G

54876123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28789432-T-C

54876209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28789333-A-T

54876222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28789320-G-C

54876222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28789320-G-T

54876301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28789246-G-T

54876336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28789211-A-T

54876401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28789166-T-A

http://identifiers.org/hco/3/GRCh38#54876458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28789109-C-A

54876769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28788609-G-C

54876769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28788609-G-T

54876906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28788486-G-T

54876919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28788473-A-G

54876942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28788450-G-A

54877007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28788390-G-A

54877007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28788390-G-T

54877028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28788370-G-T

54877060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28788339-A-G

54877076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28788325-C-T

http://identifiers.org/hco/3/GRCh38#54877077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28788324-A-C

http://identifiers.org/hco/3/GRCh38#54877083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28788318-C-A

54877087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28788314-G-T

http://identifiers.org/hco/3/GRCh38#54877102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28788299-A-C

54877102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28788299-A-G

54877105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28788296-G-A

54878308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28787078-T-G

54878334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28787052-C-T

54878458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28786930-G-A

54878780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28786634-T-A

54878780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28786634-T-C

54878863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28786553-T-C

http://identifiers.org/hco/3/GRCh38#54878869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28786547-A-C

54878869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28786547-A-G

54878892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28786431-T-A

http://identifiers.org/hco/3/GRCh38#54878894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28786429-C-A

54878930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28786382-A-G

54878989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28786304-A-G

54879104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28786187-A-G

http://identifiers.org/hco/3/GRCh38#54879182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28786114-C-A

54879182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28786114-C-T

54879234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28786062-G-T

http://identifiers.org/hco/3/GRCh38#54879260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28786033-C-A

54879304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28785943-A-T

54879333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28785918-T-C

54879796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28785482-T-C

54879813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28785466-C-T

54880004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28785312-A-G

54880154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28785166-G-A

54880170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28785150-C-T

54880182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28785138-A-G

54880216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28785117-G-T

54880426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28784920-G-A

54880527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28784816-G-A

54880527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28784816-G-T

http://identifiers.org/hco/3/GRCh38#54880558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28784784-A-C

54880932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28784358-A-T

54881268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28784098-G-C

54881390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28783981-T-C

54881454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28783918-G-A

54881752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28783706-G-A

54882135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28783485-G-T

54882747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28782854-G-A

54882781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28782819-G-A

54882847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28782757-G-A

54883782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28782088-T-A

54883782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28782088-T-C

54883833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28782059-C-T

54884188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28781826-C-G

54884256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28781764-T-C

54884388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28781699-A-T

54884401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28781686-T-C

54884431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28781668-A-G

54884506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28781610-C-T

54884933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28780915-T-G

54885076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28780793-G-A

54885134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28780756-A-G

54885134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28780756-A-T

http://identifiers.org/hco/3/GRCh38#54885195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28780691-C-A

54885195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28780691-C-T

54885201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28780684-C-T

54885368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28780522-T-C

54885444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28780446-G-A

54885639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28780257-G-T

54885673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28780222-G-A

54885673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28780222-G-C

54885673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28780222-G-T

54885719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28780190-A-G

http://identifiers.org/hco/3/GRCh38#54886144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28779802-A-C

54886148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28779798-A-G

54886183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28779747-A-G

54886220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28779711-T-C

54886326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28779584-A-G

54886456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28779393-C-T

http://identifiers.org/hco/3/GRCh38#54887251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28778627-C-A

54887251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28778627-C-T

54887269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28778593-T-C

54887341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28778540-G-A

54887357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28778524-G-A

54887391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28778498-C-T

54887394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28778495-T-A

http://identifiers.org/hco/3/GRCh38#54887463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28778427-A-C

54887535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28778356-A-G

54887673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28778227-A-G

54887737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28778155-C-T

http://identifiers.org/hco/3/GRCh38#54887810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28778083-C-A

http://identifiers.org/hco/3/GRCh38#54887818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28778075-C-A

54887818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28778075-C-T

54887860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28778035-G-T

54888202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28777694-A-G

54888309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28777589-G-A

54888827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28777161-C-T

54889017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28776976-G-C

54889089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28776899-T-C

54889164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28776826-T-C

54889230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28776703-C-G

54889230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28776703-C-T

54889333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28776592-G-A

54889482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28776294-G-A

54889804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28775996-G-A

54889879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28775922-G-A

54890104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28775713-C-T

54890181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28775645-T-C

54890463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28775257-T-C

54890526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28775194-A-G

54890675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28775077-G-A

54890675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28775077-G-C

54890763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28774995-G-A

54891062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28774739-G-A

http://identifiers.org/hco/3/GRCh38#54891260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28774550-C-A

54891260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28774550-C-T

54891283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28774528-A-G

54891326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28774484-T-C

54891471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28774339-A-G

54891745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28774088-G-C

54891822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28774017-T-G

54891879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28773962-T-G

54891902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28773940-G-C

http://identifiers.org/hco/3/GRCh38#54892036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28773810-C-A

54892059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28773775-T-C

54892147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28773688-T-A

54892214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28773622-G-T

54892302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28773540-C-T

54892374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28773478-G-A

54892429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28773419-G-A

54892482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28773384-A-G

54892529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28773336-T-A

54892651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28773208-T-A

http://identifiers.org/hco/3/GRCh38#54892756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28773103-C-A

54892756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28773103-C-T

54892848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28770345-A-G

54896569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28767790-G-T

http://identifiers.org/hco/3/GRCh38#54896585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28767774-C-A

54896585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28767774-C-T

54896592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28767767-G-A

54896592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28767767-G-T

54896597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28767762-G-A

54896597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28767762-G-T

54896710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28767661-T-A

54896789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 28767585-G-A

54896822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 28767552-G-A

54896822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 28767552-G-T

54896902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28767486-T-C

54896966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 28767434-G-A

54898889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28766306-A-G

54898936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28766276-T-C

54899005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28766226-A-G

54899054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28766180-T-C

http://identifiers.org/hco/3/GRCh38#54899090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28766145-A-C

54899224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28766030-A-G

54899263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28766000-A-G

54899294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28765968-T-C

54899324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28765939-A-G

54899575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28765708-A-G

54899583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28765700-A-G

54899836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28765488-T-A

http://identifiers.org/hco/3/GRCh38#54899964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28765381-A-C

54900144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28765021-T-G

54900392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28764788-T-G

54900569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28764641-G-A

54900611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28764593-T-C

54900712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28764494-G-A

54900712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28764494-G-T

54900734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28764470-C-G

http://identifiers.org/hco/3/GRCh38#54901041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#28764157-C-A

54901041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28764157-C-T