93447141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466817-T-C

93447607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466347-C-G

93447715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466271-C-T

93447738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466240-C-T

93447974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466013-C-T

93448795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12463284-G-C

93449058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12463045-C-G

93451322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12460703-G-A

93451554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12460491-A-G

http://identifiers.org/hco/8/GRCh38#93451948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12460292-C-A

http://identifiers.org/hco/8/GRCh38#93452162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12460112-A-C

93452162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12460112-A-G

93452164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12460110-A-G

93452185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12460089-A-G

93452288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12459975-C-G

93452940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12459331-C-T

93452947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12459324-G-T

93452962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12459309-A-G

93453162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12459102-G-A

93453162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12459102-G-C

93453347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458926-A-G

93453509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458855-C-T

93453531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458831-A-G

93453531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458831-A-T

93453540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458822-T-C

93456086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458553-G-A

93456106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458533-C-T

93456173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458470-G-A

93456386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458257-G-T

93456426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458217-A-G

93457048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458117-C-T

93457104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458060-G-A

93457954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12457523-T-G

93458218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12457230-G-A

93458442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12457034-T-G

93458480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12456996-C-G

93458480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12456996-C-T

http://identifiers.org/hco/8/GRCh38#93458482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12456994-C-A

http://identifiers.org/hco/8/GRCh38#93458682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12456809-A-C

93458783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12456712-G-A

93458810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12456687-G-A

93460380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12454934-G-A

93460519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12454815-G-A

93460797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12454584-C-T

93461333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12454088-T-C

93461352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12454071-T-C

93464207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453752-G-A

93464538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453377-G-T

http://identifiers.org/hco/8/GRCh38#93464573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12453344-C-A

93464573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453344-C-G

93464664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453261-C-G

93464871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453103-T-G

93464893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453082-G-C

93464907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453069-A-G

http://identifiers.org/hco/8/GRCh38#93465125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12452854-C-A

93465260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12452191-C-G

93465260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12452191-C-T

93465379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12452075-C-T

93465537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451939-C-G

93465582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451895-T-C

93465591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451886-T-A

93465909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451612-C-T

93465926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451595-T-C

93465963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451558-A-G

93465964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451557-G-A

93466204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451322-T-G

93466212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451314-A-T

93466302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451237-G-C

93471978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451136-T-C

http://identifiers.org/hco/8/GRCh38#93472329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12450786-A-C

93472668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12450470-G-C

93472706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12450432-A-G

93472878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12450294-T-C

93474748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12444505-C-T

93474818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12444438-G-A

93475068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12444256-A-T

93475123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12444202-C-T

http://identifiers.org/hco/8/GRCh38#93481442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12428361-C-A

93491240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12426251-T-C

93491312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12426175-T-C

93491485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12425981-T-C

93491510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12425956-T-C

93491515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12425951-T-C

93491638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12425856-T-G

93492221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12425305-T-C

93492393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12425073-G-T

93492643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12424834-T-A

93492656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12424821-T-C

http://identifiers.org/hco/8/GRCh38#93492881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12424647-A-C

93493502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12424145-T-C

http://identifiers.org/hco/8/GRCh38#93493789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12423891-C-A

93493789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12423891-C-T

93493860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12423814-A-G

93493971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12423717-T-G

93494013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12423657-T-A

93494414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12423118-G-T

93494606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422952-G-C

http://identifiers.org/hco/8/GRCh38#93494627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12422931-A-C

93494809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422730-T-C

93494843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422700-C-T

93494895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422651-G-C

93494952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422627-A-G

93495188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422509-C-G

93495203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422500-G-A

93495581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422120-T-C

93497690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419636-T-C

93497690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419636-T-G

http://identifiers.org/hco/8/GRCh38#93498279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12418986-C-A

http://identifiers.org/hco/8/GRCh38#93498317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12418948-A-C

93498317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418948-A-G

http://identifiers.org/hco/8/GRCh38#93498421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12418848-A-C

93498655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418409-C-T

93498708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418356-G-C

93498708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418356-G-T

http://identifiers.org/hco/8/GRCh38#93498741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12418325-A-C

93498742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418324-A-G

93499043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418020-G-T

93499283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12417769-T-C

93499335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12417722-T-A

93499458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12417615-G-A

93499799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12417309-G-A

93500034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12416233-T-A

93501325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12415143-A-G

93501348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12415120-T-C

93501424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12415061-T-G

93501485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12414997-G-A

93501677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12414806-C-G

93501982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12414528-C-T

93502074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12414436-T-G

93502329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12414194-C-G

93502350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12414174-C-T

93503527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413256-C-T

93503640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12413144-C-T

93503766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413018-C-T

93503969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412821-T-C

http://identifiers.org/hco/8/GRCh38#93504192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12412597-C-A

93505182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12411310-G-A

93505447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12411063-A-G

93505454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12411056-C-T

93505575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12410919-C-G

93505575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12410919-C-T

93505576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12410918-G-A

93505703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12410807-G-A

93505764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12410748-A-G

93505790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12410741-T-A

93506030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12409749-G-C

93506495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12409364-T-C

93506574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12409287-T-C

93506766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12409088-C-T

93506837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12409017-G-A

93506844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12409011-T-C

93506877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408979-G-A

93507109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408761-T-C

http://identifiers.org/hco/8/GRCh38#93507493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12408386-A-C

93507530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408355-G-A

93507821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12407976-T-G

http://identifiers.org/hco/8/GRCh38#93508109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12407584-A-C

93508155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12407538-T-C

93508520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12407193-G-A

93518243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12403880-C-G

93518243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12403880-C-T

93518290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12403833-G-A

93518367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12403761-T-C

93518575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12398220-G-T

http://identifiers.org/hco/8/GRCh38#93518664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12398141-C-A

93518664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12398141-C-T

93518738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12398068-T-C

93518769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12398035-G-A

93518769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12398035-G-T

http://identifiers.org/hco/8/GRCh38#93518780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12398024-A-C

93518897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12397817-G-A

93519029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12397686-G-C

93519213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12397511-G-T

93519235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12397489-T-G

93519364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12397381-A-G

http://identifiers.org/hco/8/GRCh38#93519443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12397286-C-A

93519443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12397286-C-G

93519466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12397275-A-G

93519476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12397265-A-T

93519535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12397206-T-C

93521150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12395529-T-C

93521174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12395505-T-C

93521431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12395248-C-G

93521431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12395248-C-T

93521507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12395154-G-C

http://identifiers.org/hco/8/GRCh38#93521511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12395150-C-A

93521512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12395149-A-G

http://identifiers.org/hco/8/GRCh38#93522180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12390071-A-C

93522459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12389858-T-C

93532526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12379614-G-A

93532697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12379453-G-A

http://identifiers.org/hco/8/GRCh38#93532755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12379395-C-A

93532755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12379395-C-T

93532779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12379371-C-T

93534796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12379172-C-T

93534851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12379119-T-A

93534894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12379073-G-A

93535180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12378357-T-C

93535180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12378357-T-G

93535229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12378307-G-A

93535393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12378152-T-C

93535458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12378114-T-A

http://identifiers.org/hco/8/GRCh38#93535673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12377909-A-C

93535673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12377909-A-T

93536687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12377785-A-T

93536726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12377749-C-T

93536924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12377569-C-T

93536961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12377548-G-C

93537221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12377262-G-C

93537222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12377261-G-A

http://identifiers.org/hco/8/GRCh38#93537344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12377153-C-A

93537438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12377055-T-C

http://identifiers.org/hco/8/GRCh38#93537617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12376898-C-A

93537676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12376840-C-T

93537801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12376716-T-C

93537801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12376716-T-G

93537897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12376602-T-C

93539889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12360067-C-T

93539899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12360055-T-G

93540035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12358866-C-T

http://identifiers.org/hco/8/GRCh38#93540076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12358822-C-A

93540076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12358822-C-T

93540094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12358804-T-C

93540118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12358780-C-T

93540153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12358748-G-A

93540778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12357123-G-T

93540797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12357107-A-T

93540837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12357066-C-T

93540907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12357001-T-C

93545084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12355084-C-G

93545098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12355070-A-G

93545098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12355070-A-T

93545304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12354878-A-G

93545551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12354638-T-C

93545753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12354453-G-A

93545777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12354431-G-A

93545938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12354290-A-G

93546110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12354067-T-C

93546111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12354066-C-T

93546236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353993-G-A

93546256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353969-A-G

http://identifiers.org/hco/8/GRCh38#93546266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12353959-A-C

93546882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353358-C-T

93546987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353242-T-C

93547160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353078-A-G

93547199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353036-G-T

93547241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12352992-T-C

http://identifiers.org/hco/8/GRCh38#93550095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12352837-C-A

93550095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12352837-C-T

93550364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12352583-T-C

93550443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12352488-T-C

93550446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12352479-A-G

93551059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12351855-A-G

93551463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12351511-A-T

93551489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12351482-T-A

93551958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12350038-G-A

93553993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12341811-T-G

93553996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12341808-T-A

93554558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12340989-A-G

93554565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12340982-T-A

93554565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12340982-T-C

93554853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12340740-G-A

93554854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12340739-A-T

93554886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12340707-C-T

93555042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12340651-T-C

93555292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12340570-T-A

93555394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12340483-C-T

93555535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12340331-A-T

93555601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12340262-C-G

93555612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12340251-G-T

http://identifiers.org/hco/8/GRCh38#93555755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12340129-C-A

93555832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12340085-C-G

93556051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12339939-T-G

93556110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12339903-C-T

93556183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12339847-G-T

93556203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12339828-T-C

93556261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12339773-G-A

93556339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12339696-G-T

93556366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12339669-G-T

93556504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12339530-T-C

http://identifiers.org/hco/8/GRCh38#93556524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12339510-A-C

http://identifiers.org/hco/8/GRCh38#93556574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12339480-C-A

http://identifiers.org/hco/8/GRCh38#93556639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12339427-C-A

93558890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12338952-G-A

93558956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12338875-A-T

93560346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12337938-G-T

93560350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12337934-C-T

93560546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12337759-A-T

93560929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12337190-A-G

93561131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12336992-T-C

93561149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12336971-C-T

93561497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12336646-C-T

93561499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12336644-T-C

93561677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12336467-C-T

http://identifiers.org/hco/8/GRCh38#93561896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12336223-A-C

http://identifiers.org/hco/8/GRCh38#93563484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12335829-C-A

93563484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12335829-C-T

93563587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12335740-C-T

93563667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12335679-T-A

93563947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12335442-T-C

93564030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: non coding transcript exon variant
orthologous variants: 12335363-G-A

http://identifiers.org/hco/8/GRCh38#93564241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12335146-C-A

93564241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12335146-C-T

93564957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12334310-T-A

93565510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12333819-C-G

93565853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12333516-C-T

93565994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12333401-A-T

93566047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12333329-G-A

93566372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12333033-T-C

93566405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12333001-A-G

93566837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12332318-A-G

93566841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12332314-T-C

93567287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12331867-G-C

93568218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12331225-T-G

93569361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12329961-T-G

93569610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12329753-A-G

93569697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12329697-A-G

http://identifiers.org/hco/8/GRCh38#93569827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12329585-A-C

93569828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12329584-C-T

93569977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12329403-C-G

93571422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12319113-G-A

93571442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12319096-G-T

http://identifiers.org/hco/8/GRCh38#93571549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12318994-A-C

93571863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12318701-T-A

93572112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12318458-T-C

93572729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12317898-C-T

93572884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12317720-C-T

93573005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12317556-A-G

http://identifiers.org/hco/8/GRCh38#93573096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12317461-A-C

93573160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12317397-G-A

http://identifiers.org/hco/8/GRCh38#93573782-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12316844-A-C

http://identifiers.org/hco/8/GRCh38#93576035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12313029-A-C

93576190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12312879-G-C

http://identifiers.org/hco/8/GRCh38#93576191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12312878-C-A

93576469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12312611-T-C

http://identifiers.org/hco/8/GRCh38#93576494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12312546-C-A

93576513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12312521-G-A

93576513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12312521-G-C

93576522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12312512-C-T

93576634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12312412-T-C

93576804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12312259-T-G

93576844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12312221-G-T

93576960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12311959-T-A

93577178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12311769-T-G

http://identifiers.org/hco/8/GRCh38#93577463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12311538-A-C

93577967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12311078-G-T

93578050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12310984-T-C

93578500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12310546-C-T

93578771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12310263-T-C

93579783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12307918-T-G

http://identifiers.org/hco/8/GRCh38#93580344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12307378-C-A

93580344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12307378-C-T

93580369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12307354-C-T

93580535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12307199-G-T

93580622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12307113-C-T

http://identifiers.org/hco/8/GRCh38#93580651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12307084-C-A

93580651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12307084-C-T

http://identifiers.org/hco/8/GRCh38#93581174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12306549-C-A

http://identifiers.org/hco/8/GRCh38#93581302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12306433-C-A

93581306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12306429-T-C

93581430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12306309-G-A

http://identifiers.org/hco/8/GRCh38#93581689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12306051-A-C

93581792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12305957-C-T

93582008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12305760-C-T

93582104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12305672-T-C

93582286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12305486-C-T

93582555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12305224-G-A

93582569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12305210-T-A

93582685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12305007-C-T

93582693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12304999-T-G

93582747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12304922-C-T

93582771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12304890-T-G

93582776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12304885-T-C

93582835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12304824-C-T

93582926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12303687-C-T

http://identifiers.org/hco/8/GRCh38#93583185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12303439-C-A

93583245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12303380-G-A

93583253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12303372-G-C

93583542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12303078-G-C

93583562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12303058-G-A

93583788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12302836-G-A

93585274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12301093-T-G

93588619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12300029-G-T

93588630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12300020-T-C

93588841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12299854-T-A

93589044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12299723-C-T

93589829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12297282-G-C

93590867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12297130-G-A

93591044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12296977-G-C

http://identifiers.org/hco/8/GRCh38#93591479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12296535-C-A

93591500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12296523-T-G

93591587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12296440-G-A

93591588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12296439-G-C

93592344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12295772-C-T

93592501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12295640-T-C

93592617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12295514-A-G

http://identifiers.org/hco/8/GRCh38#93593098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12294003-A-C

93593261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12293860-T-C

93593598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12293575-G-A

93593598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12293575-G-T

93593629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12293550-T-C

93593657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12293522-C-T

93593669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12293510-G-A

93593816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12293370-T-C

http://identifiers.org/hco/8/GRCh38#93593877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12293303-C-A

93593930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12293259-T-C

93593961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12293234-A-T

93594017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12293177-C-T

93594167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12293047-C-T

93594491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12292521-A-G

93594540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12292475-A-G

93594583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12292430-C-T

93594838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12291736-A-G

93595112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12291461-T-C

93595272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12291317-C-T

93595366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12291223-G-A

http://identifiers.org/hco/8/GRCh38#93595555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12291055-A-C

93596113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12290155-A-T

93596119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12290149-G-C

93596536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12289784-C-T

93596709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12289614-T-C

93597291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12289075-C-T

93597297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12289069-G-A

93597297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12289069-G-T

93597334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12289032-G-A

93598337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12288287-G-A

http://identifiers.org/hco/8/GRCh38#93598346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12288278-C-A

93598346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12288278-C-T

93598360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12288264-C-T

93598540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12288088-C-G

93598560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12288041-G-A

93599415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12287171-T-C

93599435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12287151-T-C

http://identifiers.org/hco/8/GRCh38#93599565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12287014-A-C

93600269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12286316-G-C

93600538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12286047-T-G

http://identifiers.org/hco/8/GRCh38#93600768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12285834-C-A

93600768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12285834-C-T

93600829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12285765-T-C

93601013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12285584-T-C

93601075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12285527-T-C

93601336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12285265-C-T

93601414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12285194-G-A

93601471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12285161-A-T

93601814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12283127-T-G

93601924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12283017-T-C

93601927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12283014-G-A

93602120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12282837-C-T

93602174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12282794-A-G

93602424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12282555-G-A

93602627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12282360-A-G

93602633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12282354-T-C

93603509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12281282-C-G

93603509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12281282-C-T

93603530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12281269-A-G

93603641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12281174-G-C

http://identifiers.org/hco/8/GRCh38#93603653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12281162-C-A

93603653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12281162-C-G

93604280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12278269-C-T

93604715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12277858-T-A

93604754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12277818-C-T

93605169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12277416-T-G

http://identifiers.org/hco/8/GRCh38#93605333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12277257-C-A

93605451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12277155-T-A

93605451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12277155-T-C

93605547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12277044-G-A

93605570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12277036-G-A

93605610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12276998-G-C

93605671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12276940-A-T

93605703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12276907-T-C

93605981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12276626-G-A

93605981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12276626-G-T

http://identifiers.org/hco/8/GRCh38#93606014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12276599-A-C

93606111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12276472-C-T

93606249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12276367-G-A

93606411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12276213-T-C

93606423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12276201-T-C

93606431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12276194-A-G

93606976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12276043-C-G

93606976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12276043-C-T

93607421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12275797-A-G

93610799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12274580-T-C

93611852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12274122-T-A

93612002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12274014-A-G

93614256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12273452-C-T

http://identifiers.org/hco/8/GRCh38#93614365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12273342-A-C

93614437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12273280-A-T

93618806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12269898-T-C

93618874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12269821-G-T

93618901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12269801-G-A

http://identifiers.org/hco/8/GRCh38#93619049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12269681-C-A

http://identifiers.org/hco/8/GRCh38#93619055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12269675-C-A

93619055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12269675-C-T

93619279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12269454-G-T

93619314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12269419-C-T

http://identifiers.org/hco/8/GRCh38#93619457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12269280-A-C

93619457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12269280-A-T

93619471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12269267-T-C

93619942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12268821-T-A

93619942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12268821-T-C

93620059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12268706-G-A

93620059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12268706-G-C

93620420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12268341-C-T

http://identifiers.org/hco/8/GRCh38#93621406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12267042-C-A

http://identifiers.org/hco/8/GRCh38#93621542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12266910-A-C

93622154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12266342-G-C

93622189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12266307-G-T

93624877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12264752-A-G

93624893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12264735-C-G

93625656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12263530-G-A

93625662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12263524-G-A

93625816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12263404-G-A

93626049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12263186-A-G

93626480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12262427-G-C

http://identifiers.org/hco/8/GRCh38#93626521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12262388-C-A

93626522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12262387-C-T

93626525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12262384-C-T

http://identifiers.org/hco/8/GRCh38#93626602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12262292-C-A

93626602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12262292-C-T

93628238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12260406-C-G

93628361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12260305-C-T

93628500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12260166-C-T

93628632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12260040-A-G

93628689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12259983-G-A

93628985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12259817-C-T

93629775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12248963-C-G

93629775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12248963-C-T

http://identifiers.org/hco/8/GRCh38#93630621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12246872-C-A

http://identifiers.org/hco/8/GRCh38#93630771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12246474-C-A

93630836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12246360-T-C

93631058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12246172-C-T

93631864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12246060-G-A

93632183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12245748-T-C

http://identifiers.org/hco/8/GRCh38#93632197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12245734-A-C

93632443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12245386-G-A

93632443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12245386-G-T

93632451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12245378-C-T

93632509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12245321-G-T

93632561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12245269-T-C

http://identifiers.org/hco/8/GRCh38#93632740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12245108-C-A

93632756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12245092-A-G

93632942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12244918-T-A

93633101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12244742-G-A

93633167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12244677-G-A

93633922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12243586-G-A

93634180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12243335-T-C

93634213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12243306-G-A

93634283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12243236-G-A

93634358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12243169-G-A

93634365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12243162-G-A

93635403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12241708-G-T

93635405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12241706-A-G

93635928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12241180-T-C

93635957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12241165-T-A

93635957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12241165-T-C

http://identifiers.org/hco/8/GRCh38#93636013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12241130-A-C

93636309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12240936-C-G

93636310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12240935-T-G

93636375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12240873-T-C

93636396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12240832-C-T

http://identifiers.org/hco/8/GRCh38#93636429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12240804-A-C

93636565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12240681-A-T

93636782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12240519-C-T

93638714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12239509-C-T

93638744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12239481-G-C

93638860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12239387-C-T

93638974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12239272-A-T

93639357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12238899-T-C

93640644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12232331-G-C

93641684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12231120-T-C

93641731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12231074-G-A

93641799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12231021-G-T

93673475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12230870-T-C

93673569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12230782-A-T

93673743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12230616-G-C

http://identifiers.org/hco/8/GRCh38#93673820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12230544-C-A

93673828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12230535-A-G

93673849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12230514-A-G

93674487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12229876-A-G

93674679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12229688-A-G

93675668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12226698-T-C

93675752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12226617-T-C

93675823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12226541-T-C

93675923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12226479-C-G

93675992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12226409-T-C

93677345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12226095-T-A

93677456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12225989-G-A

93678063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12225700-C-T

93678179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12225556-G-C

http://identifiers.org/hco/8/GRCh38#93678180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12225555-A-C

93678220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12225510-G-A

93678380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12225352-T-C

93678558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12225209-T-G

93678632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12225131-C-T

93679550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12224099-C-T

93679588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12224061-G-A

93694946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12177384-C-T

93698207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12174722-G-A

http://identifiers.org/hco/8/GRCh38#93698364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12174571-A-C

93698395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12174540-T-C

http://identifiers.org/hco/8/GRCh38#93698412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12174523-C-A

93698465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12174479-C-T

93698481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12174463-G-T

93698504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12174454-G-T

http://identifiers.org/hco/8/GRCh38#93698511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#12174447-C-A

http://identifiers.org/hco/8/GRCh38#93698601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#12174349-C-A

93700164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12172069-A-G

93700164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12172069-A-T

93700189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43644
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12172059-C-T