104430183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: non coding transcript exon variant
orthologous variants: 42296834-C-T

104431054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42297704-C-G

104431054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42297704-C-T

104431279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42297933-C-G

104431279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42297933-C-T

http://identifiers.org/hco/2/GRCh38#104431287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42297941-A-C

104431397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42298050-G-A

104431397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42298050-G-T

http://identifiers.org/hco/2/GRCh38#104431450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42298103-C-A

http://identifiers.org/hco/2/GRCh38#104431966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42298647-C-A

104432455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42299178-G-T

104432456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42299179-C-T

104432558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42299281-C-G

http://identifiers.org/hco/2/GRCh38#104433152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42299841-C-A

104433181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42299870-G-T

104433517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42300159-A-G

104433517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42300159-A-T

http://identifiers.org/hco/2/GRCh38#104433654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42300313-C-A

http://identifiers.org/hco/2/GRCh38#104433869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42300513-C-A

http://identifiers.org/hco/2/GRCh38#104434309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42300944-C-A

http://identifiers.org/hco/2/GRCh38#104434377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42301012-C-A

104434377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42301012-C-T

http://identifiers.org/hco/2/GRCh38#104434431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42301066-C-A

104434431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42301066-C-T

http://identifiers.org/hco/2/GRCh38#104434585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#42301223-C-A

http://identifiers.org/hco/2/GRCh38#104434587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#42301225-C-A

104434587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42301225-C-T

104434691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42301313-G-T

104434783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42301485-G-T

104434789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42301491-G-T

104434814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42301516-G-A

104434886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42301596-C-G

104434886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42301596-C-T

104435323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42302047-G-A

104435323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42302047-G-C

104435814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42302505-T-A

104435885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42302578-T-C

104435915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42302620-A-G

104436026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42302723-G-T

http://identifiers.org/hco/2/GRCh38#104436033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42302730-C-A

104436071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42302763-G-T

104436164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42302847-T-C

104436266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42302908-G-A

104436466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42303041-A-T

104436751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42303299-C-T

104436878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42303437-A-G

104436879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42303438-G-A

104436942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42303494-A-G

104437158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42303683-C-T

104437199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42303715-G-A

104437521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42304089-C-T

http://identifiers.org/hco/2/GRCh38#104437523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42304091-C-A

104437523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42304091-C-T

http://identifiers.org/hco/2/GRCh38#104437589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42304133-A-C

104437807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42304344-G-T

104437955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42304509-C-G

104437955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42304509-C-T

104438425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42304912-G-A

104438446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42304933-T-C

104438561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42305022-T-G

104438771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42305532-A-G

104439033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42305798-G-A

104439164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42305930-G-A

104439339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42306133-G-T

http://identifiers.org/hco/2/GRCh38#104439352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42306146-C-A

104439562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42306355-C-T

104440383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42307350-A-G

104440537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42307431-T-C

104441383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42308325-T-A

104441517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42308457-G-A

104441760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42308697-G-A

104442104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42309006-A-G

http://identifiers.org/hco/2/GRCh38#104444011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42311138-C-A

104444364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42311485-A-G

104444533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42311666-G-A

104444637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42311746-T-C

http://identifiers.org/hco/2/GRCh38#104444673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42311773-C-A

104444673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42311773-C-T

104444677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42311777-G-A

104444752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42311831-C-T

104444968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42312017-A-G

104445008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42312046-C-T

104445096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42312161-C-T

104445451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42312481-C-G

104445453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42312483-G-A

104445482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42312534-C-T

104445757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42313210-G-A

104445895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42313317-C-T

104446212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42313567-C-G

104446212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42313567-C-T

104446213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42313568-G-A

104446466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42313849-C-T

104446520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42313907-A-G

104446530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42313925-C-T

http://identifiers.org/hco/2/GRCh38#104446601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42313991-C-A

104446696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42314077-C-T

104446910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42314295-G-A

104447455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42314908-T-A

104448192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42315828-G-A

104448702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42316365-T-C

104448930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42316579-A-G

104448947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42316591-G-T

104449058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42316704-T-C

104449527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42317260-A-G

http://identifiers.org/hco/2/GRCh38#104449556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42317289-C-A

104449927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42317615-G-T

104449929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42317617-T-A

104449984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42317684-C-T

104450343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42318010-C-T

104450424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42318085-T-A

104450424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42318085-T-C

104454137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42321320-T-C

104454152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42321335-G-C

104454171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42321351-T-C

104454171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42321351-T-G

104454245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42321426-A-G

104454441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42321578-C-G

104462120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42329554-G-A

104462600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42330028-G-A

104462600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42330028-G-T

104462924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42330434-C-T

104463007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42330528-T-C

104463007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42330528-T-G

104463156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42330706-T-A

104463224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42330763-T-A

104463224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42330763-T-G

104464414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42331071-C-T

http://identifiers.org/hco/2/GRCh38#104465154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42331392-A-C

104465205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42331443-G-A

104465205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42331443-G-T

104465389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42331631-G-A

104465590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42331841-T-C

104465930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42332086-T-C

104466005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42332159-T-C

http://identifiers.org/hco/2/GRCh38#104466013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42332167-C-A

104466013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42332167-C-T

104466178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42332260-T-C

104466271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42332349-T-G

104466324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42332400-T-C

http://identifiers.org/hco/2/GRCh38#104466354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42332430-C-A

104466463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42332536-A-G

http://identifiers.org/hco/2/GRCh38#104466756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42332852-C-A

104466821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42332919-T-G

104468251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42333619-G-A

104468254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42333622-A-G

104468261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42333629-C-T

104468344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42333715-G-C

104468344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42333715-G-T

104468668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42334000-C-T

104468674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42334006-A-T

104468700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42334032-T-A

http://identifiers.org/hco/2/GRCh38#104469700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42335033-A-C

104469759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42335091-C-T

104469867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42335199-A-G

104469885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42335217-G-T

104470060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42335386-G-A

104470060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42335386-G-T

104470099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42335427-T-C

104470147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42335456-G-C

104470167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42335476-T-C

104470241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42335563-G-A

104470262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42335584-C-T

104470304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42335627-G-A

104470348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42335671-G-T

104470353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42335676-C-T

http://identifiers.org/hco/2/GRCh38#104470787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42336082-A-C

104470802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42336097-T-C

104470808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42336103-C-T

104470823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42336114-G-A

104470823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42336114-G-C

104471030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42336352-G-C

http://identifiers.org/hco/2/GRCh38#104471266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42337187-C-A

104471389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42337311-T-C

104471459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42337369-T-C

104473414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42337735-T-C

104473472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42337794-A-G

104473819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42338135-G-C

104474002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42338303-A-G

104474414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42338668-C-T

http://identifiers.org/hco/2/GRCh38#104474505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42338764-A-C

http://identifiers.org/hco/2/GRCh38#104474600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42338859-C-A

104474707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42338959-G-T

104474803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42339042-T-C

http://identifiers.org/hco/2/GRCh38#104474893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42339133-C-A

104474927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42339163-C-T

104475006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42339240-C-G

104475142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42339374-C-T

104475221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42339453-G-A

104475276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42339488-C-T

104475574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42339776-C-T

104475601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42341444-A-G

104475601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42341444-A-T

104475652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42341498-A-G

104475652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42341498-A-T

104476085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42341889-T-A

104476309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42342108-G-C

104476451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42342244-G-A

104476454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42342247-A-G

104476469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42342280-T-C

104476674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42342572-G-A

104476850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42342732-T-A

104477190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42343079-T-C

104477294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42343170-C-T

104477320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42343193-T-G

104477383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42343256-T-C

http://identifiers.org/hco/2/GRCh38#104477404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42343276-A-C

104477493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42343351-T-C

104477781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42343625-C-T

104478144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42343945-G-A

104478607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42344070-G-T

104478680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42344142-G-A

104478696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42344158-A-T

104479380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42344744-C-T

http://identifiers.org/hco/2/GRCh38#104479527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42344885-A-C

104479527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42344885-A-G

104480310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42345134-A-G

104480762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42345611-A-G

104480974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42346512-G-C

104481005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42346543-T-G

104481048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42346582-C-G

http://identifiers.org/hco/2/GRCh38#104481055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42346583-A-C

104481055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42346583-A-G

104481088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42346616-T-C

104481101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42346621-A-G

104481184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42346793-G-T

104481263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42346872-G-C

104481273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42346878-A-G

104481426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42347030-C-T

104481427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42347031-G-A

104481442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42347046-A-G

104481652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42347260-G-T

104482006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42348370-C-T

http://identifiers.org/hco/2/GRCh38#104482037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42348387-A-C

104482037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42348387-A-G

104482049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42348402-T-A

104482118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42348466-G-A

104482118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42348466-G-T

104482313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42348659-C-T

104482537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42348842-G-A

http://identifiers.org/hco/2/GRCh38#104486038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42360150-A-C

104486038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42360150-A-T

104486066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42360177-G-C

104486148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42360253-C-G

104486177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42360282-C-T

http://identifiers.org/hco/2/GRCh38#104486196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42360300-C-A

104486221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42360314-C-G

104486248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42360339-C-T

http://identifiers.org/hco/2/GRCh38#104486435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42360523-C-A

104486442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42360530-C-T

104486492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42360567-G-A

104486492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42360567-G-C

104486670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42360717-C-T

104486696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42360737-T-C

104487028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42361010-T-G

http://identifiers.org/hco/2/GRCh38#104487363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42361304-C-A

104487392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42361331-T-C

104487570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42361498-C-T

104487660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42361632-T-A

104487857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42363058-G-T

104487964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42363155-T-C

104488392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42363679-G-T

104488432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42363718-T-A

104488555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42363839-G-T

104488578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42363862-T-A

104488643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42363927-A-T

http://identifiers.org/hco/2/GRCh38#104489047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42364300-C-A

http://identifiers.org/hco/2/GRCh38#104489135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42364389-C-A

104489302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42364548-T-C

104489633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 42364844-G-A

104489820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42364996-A-G

104489881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42365056-C-T

104490963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42366837-C-T

104491011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42366929-A-G

104495392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42384278-C-T

104495460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42384344-C-G

104495509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42384401-T-C

104496093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42385212-T-A

104496357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42385427-G-A

104496500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42385881-A-T

104496664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42386052-C-T

104496677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42386065-C-T

104496688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42386076-G-T

104496763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42386151-C-G

104496811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42386230-G-A

104496824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42386243-C-G

104497151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42386573-A-G

http://identifiers.org/hco/2/GRCh38#104497348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42386770-C-A

104497609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42387016-T-C

104497797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42387178-G-A

104498220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42387943-G-A

104498220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42387943-G-T

104498293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42388025-A-G

104498328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42388061-G-T

104498774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42388253-G-A

104498948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42388405-G-A

104498977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42388435-G-A

104499069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42388861-G-A

104499164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42388959-A-G

104499173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42388968-G-T

104499286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42389085-A-G

104499359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42389151-C-T

104499447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42389238-C-G

104499602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42389351-G-A

104500291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42390060-T-C

104500436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42390180-T-C

104500497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42390237-G-A

104500497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42390237-G-C

104500683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42390415-A-T

http://identifiers.org/hco/2/GRCh38#104500758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42390488-C-A

104500964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42390635-T-C

http://identifiers.org/hco/2/GRCh38#104501075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42390766-C-A

http://identifiers.org/hco/2/GRCh38#104501128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42390808-C-A

104501128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42390808-C-T

104501184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42390865-G-C

104501451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42391143-G-A

104501451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42391143-G-C

104501479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42391171-G-A

104502234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42391965-G-A

104502234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42391965-G-T

http://identifiers.org/hco/2/GRCh38#104502395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42392125-A-C

104502456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42392199-A-G

104502500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42392271-T-A

104502972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42392662-A-G

http://identifiers.org/hco/2/GRCh38#104503018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42392702-C-A

http://identifiers.org/hco/2/GRCh38#104503049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42392739-C-A

104503142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42392821-G-T

104503247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42392922-A-G

104504147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42393823-G-A

104504270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42393947-C-T

104504416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42394091-G-A

104504449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42394124-G-A

104504466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 42394178-G-T

104504541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42394282-G-A

104504558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42394299-T-C

http://identifiers.org/hco/2/GRCh38#104504891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42394637-C-A

104504891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42394637-C-T

104505199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42394938-G-A

104505238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42394971-T-C

104505490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42395197-A-T

104505680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42395399-C-T

http://identifiers.org/hco/2/GRCh38#104505721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42395440-C-A

104505721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42395440-C-T

104505814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42395537-T-C

104505851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42395575-G-T

104505867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 42395591-G-A

104505867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 42395591-G-T

104505882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42395611-G-A

104505882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42395611-G-C

104505922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42395650-G-T

http://identifiers.org/hco/2/GRCh38#104505926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42395654-A-C

104506089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42395801-A-G

104506112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42395831-G-T

104506272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42395928-G-A

http://identifiers.org/hco/2/GRCh38#104506273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42395929-C-A

104506273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42395929-C-T

104506284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42395941-G-T

http://identifiers.org/hco/2/GRCh38#104506495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42396007-C-A

104506495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42396007-C-G

104506495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42396007-C-T

104506522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42396030-A-G

104506938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42396247-A-G

104507049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42396367-A-T

104507064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42396396-C-T

104507144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42396481-C-T

104507229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 42396567-C-T

104507273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42396609-G-A

104507273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42396609-G-T

http://identifiers.org/hco/2/GRCh38#104507309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42396645-C-A

104507309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42396645-C-T

104507373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42396713-A-T

104507407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 42396739-G-A

104507428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42396757-C-G

104507428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42396757-C-T

104507454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42396780-T-C

104507660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42396975-T-C

http://identifiers.org/hco/2/GRCh38#104508613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42397959-A-C

http://identifiers.org/hco/2/GRCh38#104508751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42398087-C-A

104508792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42398129-G-A

104508854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42398205-A-G

104508904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42398248-T-G

104511564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42401518-C-T

104511639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42401591-T-C

104511849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42401797-G-A

http://identifiers.org/hco/2/GRCh38#104511959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42401907-A-C

104511959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42401907-A-G

104511963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42401911-G-A

104512075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42402027-A-G

104512148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42402112-T-C

104512173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42402127-C-T

http://identifiers.org/hco/2/GRCh38#104512213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42402158-C-A

104512213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42402158-C-T

http://identifiers.org/hco/2/GRCh38#104512243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42402188-C-A

104512247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42402192-G-T

http://identifiers.org/hco/2/GRCh38#104512254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42402199-C-A

104512384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42402276-G-A

104512384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42402276-G-C

104512384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42402276-G-T

104514576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42403102-G-A

104514576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42403102-G-T

104514615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42403141-T-C

104514753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42403271-C-T

104514794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42403303-G-C

104514991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42403498-G-T

104515006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42403514-A-G

104515014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42403522-A-G

104515149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42403650-C-T

104515215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42403716-A-G

104515222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42403723-G-C

104515233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42403728-G-A

104515330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42403863-A-G

http://identifiers.org/hco/2/GRCh38#104515350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42403883-C-A

104515377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42403911-T-G

104515395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42403929-G-A

104515407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42403947-G-C

104515538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42404056-C-T

104515540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42404058-C-G

104515540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42404058-C-T

104515543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42404061-G-A

104515544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42404062-G-A

104515553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42404071-T-G

104515571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42404089-C-T

104515601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42404118-T-A

104515635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42404151-C-G

104515751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42404266-A-G

104515757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42404272-T-C

http://identifiers.org/hco/2/GRCh38#104515867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42404373-C-A

104515889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42404395-A-G

104516059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42404563-T-A

104516376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42404946-C-T

104516702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42405269-G-T

104517060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42405626-A-T

http://identifiers.org/hco/2/GRCh38#104517400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42405966-A-C

104517510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42406070-C-G

104517546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42406107-A-G

104517840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42406403-G-A

104517981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42406548-A-G

104518015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42406579-T-C

104518070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: non coding transcript exon variant
orthologous variants: 42406622-A-G

http://identifiers.org/hco/2/GRCh38#104518087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42406639-C-A

104518108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42406659-T-C

104518108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42406659-T-G

104518113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42406664-T-C

104518273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42406767-A-G

http://identifiers.org/hco/2/GRCh38#104518431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42406916-C-A

http://identifiers.org/hco/2/GRCh38#104518918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42407251-C-A

104518948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42407281-C-T

104518959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42407292-C-T

104520043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42407845-G-A

http://identifiers.org/hco/2/GRCh38#104520283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42408104-C-A

104520330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42408159-G-T

104520338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42408167-C-T

104520589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42408429-G-A

104520589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42408429-G-T

104520630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42408454-A-G

104520630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42408454-A-T

104520646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42408470-G-C

104520654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42408478-G-T

104520680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42408508-T-G

104520749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42408578-T-C

104521170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42408934-T-C

http://identifiers.org/hco/2/GRCh38#104521241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42408995-C-A

104521241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42408995-C-T

http://identifiers.org/hco/2/GRCh38#104521495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42409229-C-A

http://identifiers.org/hco/2/GRCh38#104521597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42409317-A-C

104524989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42409934-T-C

104525111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42410050-A-G

104525111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42410050-A-T

104525337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42410280-G-A

http://identifiers.org/hco/2/GRCh38#104525392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42410333-C-A

104526220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42410697-G-A

104526258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42410735-A-G

104526301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42410776-G-A

104526362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42410821-G-A

104526730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42411311-G-A

104526788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42411354-G-A

104526839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42411402-T-C

http://identifiers.org/hco/2/GRCh38#104527152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42411731-C-A

104527152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42411731-C-G

104527182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42411754-G-A

104527378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42411922-C-T

104527496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42411995-A-T

104528162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42412639-T-A

104528162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42412639-T-G

http://identifiers.org/hco/2/GRCh38#104528172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42412649-C-A

104528247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42412715-C-T

104528495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42412953-T-G

104528500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42412958-C-T

104528650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42413312-C-T

104530968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42414716-C-T

http://identifiers.org/hco/2/GRCh38#104531006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42414754-A-C

104531023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42414771-T-C

104531699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42415576-G-A

104531809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42415642-T-G

104532106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42415879-A-G

104532133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42415904-A-G

104532287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42416063-C-T

104532433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42416226-T-C

104532459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42416239-A-G

104532514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: non coding transcript exon variant
orthologous variants: 42416278-C-T

104532559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: non coding transcript exon variant
orthologous variants: 42416336-C-T

104532633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: non coding transcript exon variant
orthologous variants: 42416404-A-G

104532653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: non coding transcript exon variant
orthologous variants: 42416420-T-A

104532653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27165
most severe consequence: non coding transcript exon variant
orthologous variants: 42416420-T-C