26393657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85168951-T-C

26394202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85169441-G-C

26394222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85169461-A-G

26394257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85169496-T-C

26394264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85169503-G-T

26394674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85169862-A-G

26394793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85169986-A-G

26394897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85170088-G-A

http://identifiers.org/hco/21/GRCh38#26394898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85170089-C-A

26394898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85170089-C-T

26395048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85170219-A-G

26395164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85170317-A-T

26395238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85170386-A-G

26395297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85170436-A-G

26395367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85170505-C-T

26395690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85170613-A-G

26395694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85170616-G-A

26395717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85170639-A-T

26395725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85170647-C-T

26395787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85170714-C-T

26395843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85170771-T-C

26396329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85170830-C-T

26396351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85170852-A-G

26396599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85171106-C-T

http://identifiers.org/hco/21/GRCh38#26396645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85171159-A-C

26396728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85171241-C-T

26396729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85171242-C-T

26396770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85171282-T-C

26396783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85171295-C-G

26396855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85171361-G-A

26396930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85171437-T-C

26397034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85171542-G-A

26397513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85171663-C-T

26397568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85171718-T-C

26397629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85171782-G-C

26397674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85171827-G-A

26397764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85171922-G-A

26397843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85171983-T-C

26398041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85172178-C-T

26398156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85172265-G-A

26398247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85172339-T-G

26399150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85172578-A-G

http://identifiers.org/hco/21/GRCh38#26400652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85174139-A-C

26400680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85174167-G-A

26400714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85174201-C-T

26400840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85174325-T-C

26402128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85174580-G-A

26402337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85174781-T-C

26402372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85174816-A-G

http://identifiers.org/hco/21/GRCh38#26402431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85174872-A-C

26402677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85175396-A-G

26402687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85175406-C-G

26402687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85175406-C-T

26402748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85175465-T-A

26402753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85175470-A-G

http://identifiers.org/hco/21/GRCh38#26402778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85175489-C-A

26402778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85175489-C-G

26402900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85175680-G-A

26403006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85175767-C-G

26403006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85175767-C-T

http://identifiers.org/hco/21/GRCh38#26403204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85175909-A-C

26403419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85176129-C-T

26403422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85176132-C-T

26403540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85176300-T-G

http://identifiers.org/hco/21/GRCh38#26403563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85176323-A-C

26403599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85176364-A-G

26403688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85176430-T-C

26404087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85176696-G-A

26404099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85176708-C-T

26404336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85176950-G-A

26404662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85177151-G-A

26404816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85177276-C-T

26404872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85182006-G-A

26405037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85182161-C-T

26405038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85182162-A-G

26405129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85182250-C-T

26405275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85182389-G-A

26405424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85182721-C-T

26405446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85182738-G-A

26405503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85182807-T-C

26405519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85182822-G-C

26405677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85182964-C-T

26405678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85182965-A-G

http://identifiers.org/hco/21/GRCh38#26405707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85182995-A-C

26405822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85183062-G-A

26405822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85183062-G-T

26405866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85183108-G-C

26405866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85183108-G-T

26405870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85183112-G-T

26405941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85183160-T-C

26405982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85183187-C-T

26406067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85183275-G-A

26406067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85183275-G-C

26406106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85183313-A-G

26406180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85183358-G-T

26406181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85183359-A-G

26406186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85183364-G-A

26406186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85183364-G-T

26406341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85183517-C-G

26406341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85183517-C-T

26406362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85183538-G-A

26406385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85183560-G-A

26406416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85183591-T-G

http://identifiers.org/hco/21/GRCh38#26407050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85184197-C-A

26407061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85184208-A-G

26407124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85184270-A-T

26407758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85184551-G-A

26408355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85184642-A-G

26408628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85184898-T-A

26408628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85184898-T-G

26408671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85184933-T-G

26408717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85184974-T-A

26408839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85185194-C-T

26408872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85185230-T-C

26408904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85185267-G-T

http://identifiers.org/hco/21/GRCh38#26408912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85185275-A-C

26408956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85185323-T-C

26409206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85186240-C-T

26409255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85186284-A-G

26409267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85186289-A-G

26409267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85186289-A-T

26409345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85186325-C-T

26409590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85186565-G-A

26409716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85186694-G-A

26409737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85186710-C-T

26409956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85186927-C-T

26410055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85187020-G-A

26410076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85187042-G-A

http://identifiers.org/hco/21/GRCh38#26410126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85187089-A-C

26410240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85187291-T-A

26410318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85187381-G-A

http://identifiers.org/hco/21/GRCh38#26410649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85187733-A-C

26410649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85187733-A-G

26410673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85187756-C-T

26410674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85187757-G-A

26410721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85187802-T-C

26410726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85187807-G-T

26410762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85187849-C-T

26410888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85187961-C-T

26411059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85188124-G-A

26411059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85188124-G-C

26411510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85188641-T-A

26411516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85188647-G-A

26411714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85188731-G-A

26411938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85188809-G-A

26412121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85188958-C-G

26412122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85188959-C-T

26412174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85189003-C-G

26412683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85189318-T-A

26412880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85189490-C-T

26412928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85189543-A-G

26412992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85189580-G-A

26412993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85189581-G-A

26412993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85189581-G-C

26413009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85189597-A-G

http://identifiers.org/hco/21/GRCh38#26413043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85189631-A-C

26413058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85189651-G-A

26413058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85189651-G-T

http://identifiers.org/hco/21/GRCh38#26413059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85189652-A-C

26413059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85189652-A-T

26413112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85189691-A-G

26413129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85189708-G-A

26413129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85189708-G-T

26413132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85189711-G-A

26413132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85189711-G-C

26413139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85189718-A-G

26413157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85189735-T-C

26413180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85189758-G-T

26413194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85189774-C-T

http://identifiers.org/hco/21/GRCh38#26413263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85189803-C-A

http://identifiers.org/hco/21/GRCh38#26413304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85189871-C-A

26413306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85189873-T-C

26413351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85189922-C-T

26415949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85191316-A-G

http://identifiers.org/hco/21/GRCh38#26415966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85191333-C-A

26415966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85191333-C-T

26415987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85191354-T-C

26415997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85191364-G-A

26416247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85191595-T-C

26416302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85191649-G-A

26416339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85191685-C-T

http://identifiers.org/hco/21/GRCh38#26416340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85191686-A-C

26416344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85191691-T-C

26416370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85191718-G-C

26416378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85191726-C-T

26416417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85191764-T-C

26416514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85191863-A-G

26416535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85191884-T-C

26416542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85191891-A-G

http://identifiers.org/hco/21/GRCh38#26416596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85191934-C-A

26416596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85191934-C-T

26416608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85191946-A-G

26416629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85191970-A-G

26416629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85191970-A-T

26416774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85192119-G-A

26416904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85192252-T-C

26416904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85192252-T-G

26416947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85192289-C-T

26417018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85192529-A-G

http://identifiers.org/hco/21/GRCh38#26417044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85192564-C-A

26417125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85192637-G-A

26417153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85192656-G-T

26417213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85192711-T-A

26423384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85194960-A-G

26423402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85194978-G-A

26423447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85195021-T-A

26423551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85195123-A-G

26423567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85195139-G-A

26423706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85195267-G-C

26423738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85195299-A-G

26428967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85199608-T-A

26428967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85199608-T-G

26428968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85199609-A-G

26429027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85199667-C-T

http://identifiers.org/hco/21/GRCh38#26429031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85199680-C-A

26429045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85199694-T-C

26429085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85199733-G-A

http://identifiers.org/hco/21/GRCh38#26429098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85199746-A-C

http://identifiers.org/hco/21/GRCh38#26429119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85199767-A-C

26429217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85199836-G-A

26429272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85199855-G-T

26429345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85199899-A-G

26429384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85199935-G-A

26429482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85200020-G-A

26429513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85200051-G-T

http://identifiers.org/hco/21/GRCh38#26429657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85200196-C-A

26429694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85200230-C-T

26429720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85200251-G-A

26430169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85200729-A-G

http://identifiers.org/hco/21/GRCh38#26430179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85200739-A-C

26430179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85200739-A-T

26430185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85200745-C-G

26431336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85201113-C-G

26431425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85201204-A-G

26431536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85201314-G-C

26431702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85201470-G-A

26431702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85201470-G-T

26431921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85201665-G-C

26432090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 85201841-A-G

26432384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85202107-G-A

26432414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85202137-G-A

26432551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85202263-G-A

26432717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85202396-C-T

26432751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85202430-C-T

26432825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85202504-A-G

26432836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85202515-C-T

26432843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85202522-T-G

26433479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85203101-G-A

26433597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85203204-T-C

26435867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85205862-A-G

26436094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85206897-A-G

26436112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85206915-G-A

26436139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85206942-A-G

26436748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85210971-C-G

26436777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85211000-C-T

26437081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85211646-A-G

26437082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85211647-T-C

26437097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85211662-T-C

26437119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85211684-A-T

26437258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85212004-T-C

26437437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85212211-T-C

26437484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85212255-T-G

26437734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85212499-G-T

26437749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85212514-T-C

http://identifiers.org/hco/21/GRCh38#26437884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85212635-C-A

26437884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85212635-C-T

26438088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85212822-G-A

26438482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85213592-C-T

26438486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85213596-C-T

26438597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85213745-A-G

26438624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85213772-G-T

26438719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85213869-G-A

26438881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85213999-C-T

26439036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85214157-T-C

26439179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85214274-T-C

26439258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85214352-G-A

26439258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85214352-G-T

26439260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85214354-T-C

26439368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85214458-G-A

26439391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85214481-A-G

26439548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85214625-A-T

http://identifiers.org/hco/21/GRCh38#26439552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85214629-A-C

26439592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85214663-A-G

http://identifiers.org/hco/21/GRCh38#26439736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85214802-C-A

http://identifiers.org/hco/21/GRCh38#26439740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85214806-C-A

26439740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85214806-C-T

26441736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85215225-C-T

26442049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85215519-G-A

http://identifiers.org/hco/21/GRCh38#26442080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85215550-C-A

http://identifiers.org/hco/21/GRCh38#26442138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85215596-C-A

26442158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85215616-C-T

26442163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85215621-A-G

26442178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85215636-A-T

26442217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85215673-A-G

26442422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85215931-A-G

26442551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85216059-A-G

26442631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85216129-G-C

26442707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85216202-A-G

26442861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85216363-T-C

26443086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85216629-G-T

26443178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85216723-C-T

26443290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85216838-T-G

26443310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85216850-A-G

http://identifiers.org/hco/21/GRCh38#26443399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85216940-C-A

26443399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85216940-C-T

26443484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85217003-A-G

26443525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85217040-G-A

26443525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85217040-G-C

26443552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85217065-C-T

26443568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85217084-C-T

26443606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85217124-T-G

26443888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85217405-C-T

26444072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85217691-T-C

26444132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85217740-T-A

26444140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85217748-T-C

http://identifiers.org/hco/21/GRCh38#26444368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85218017-A-C

26444392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85218041-T-A

26444392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85218041-T-C

26444582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85218274-G-T

26444774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85218445-G-T

http://identifiers.org/hco/21/GRCh38#26444776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85218447-C-A

26444776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85218447-C-T

http://identifiers.org/hco/21/GRCh38#26444821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85218476-C-A

26444927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85218540-G-A

26444987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85218600-C-G

26445099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85218687-G-C

26445258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85218896-G-A

26445269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85218962-G-A

26445280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85218981-T-C

26445558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85219370-T-C

26445607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85219450-C-T

26445630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85219533-T-G

http://identifiers.org/hco/21/GRCh38#26448557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85222169-C-A

26448635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85222221-C-T

26448875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85222420-T-G

26448922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85222467-C-T

26448936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85222481-C-G

26448936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85222481-C-T

26448968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85222511-C-T

26449219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85226019-C-G

26449239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85226039-C-T

26450071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85228366-C-T

26450279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85228531-C-T

26450300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85228552-C-T

26450419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85228673-G-T

26450527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85228770-G-T

26450559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85228797-G-A

26450561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85228799-T-A

26451305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85229578-G-A

26451666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85230197-C-T

26451877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85230504-A-G

26451892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85230519-C-G

http://identifiers.org/hco/21/GRCh38#26451939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85230563-A-C

http://identifiers.org/hco/21/GRCh38#26453337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85231277-C-A

26453352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85231290-C-G

26453387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85231321-G-A

26453525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85231440-T-C

26453723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85231595-A-G

26453771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85231645-C-T

26453815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85231689-A-T

26453931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85231810-C-G

26456324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85235799-T-C

26456882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85236305-G-A

26457259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85236678-C-T

26457295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85236714-G-C

26457355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85236767-A-G

26457389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85236799-A-G

26461173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85240422-T-G

26461228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85240472-C-G

26461424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85240661-A-G

26461426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85240663-T-C

26461456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85240696-G-T

26461666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85241299-A-G

26461845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85241470-T-C

26462239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85242234-G-A

26462327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85242312-C-T

26462487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85242449-T-C

26462522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85242485-C-G

26462524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85242487-A-G

26463512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85242784-T-G

26463600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85242873-C-T

26463654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85242919-G-T

26463661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85242926-T-C

26463667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85242931-G-A

26463682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85242946-G-T

26463686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85242950-C-T

26463706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85242966-T-C

http://identifiers.org/hco/21/GRCh38#26463712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85242972-A-C

26463722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85242982-G-A

26463750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243010-A-G

26463775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243035-T-C

26463783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243044-G-T

26463838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243100-T-C

26463856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243118-A-G

26463861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243123-T-C

http://identifiers.org/hco/21/GRCh38#26463862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85243124-C-A

26463896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243154-A-G

26463898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243156-G-A

26463956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243212-T-C

26463972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243227-C-G

26464015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243269-G-A

26464076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243345-G-A

26464086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243355-C-T

26464154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243394-C-T

26464155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243395-T-C

26464238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243474-G-A

26464238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243474-G-T

http://identifiers.org/hco/21/GRCh38#26464262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85243498-C-A

26464268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243504-A-G

26464271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243507-G-C

26464272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243508-G-A

26464313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243546-G-A

26464363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243600-C-T

26464365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243602-C-T

26464391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243629-A-G

26464417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243655-G-A

26464481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243717-G-A

26464517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243755-T-C

http://identifiers.org/hco/21/GRCh38#26464530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85243768-C-A

26464530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243768-C-T

26464546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243784-C-T

26464569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243807-A-G

26464584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243822-T-A

26464584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243822-T-G

26464586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243824-T-C

26464590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243828-T-C

26464685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243954-G-C

26464714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85243984-A-G

26464750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85244018-C-T

26464767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85244034-G-A

http://identifiers.org/hco/21/GRCh38#26464941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85244141-C-A

26465010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85244212-G-A

26465828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85246643-A-T

26465999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85246780-A-G

26466072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85246852-T-C

26466123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85246899-C-T

http://identifiers.org/hco/21/GRCh38#26466246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85249775-C-A

26466246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85249775-C-T

26466331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85249858-C-T

26466494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85250016-A-G

26466558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85250079-G-A

26466558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85250079-G-T

26466693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85250208-A-G

26466705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85250220-A-G

26466753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85250270-A-G

26466791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85250307-G-A

26466791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85250307-G-T

26466800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85250316-C-T

http://identifiers.org/hco/21/GRCh38#26466876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85250386-C-A

26466876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85250386-C-T

http://identifiers.org/hco/21/GRCh38#26466883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85250393-C-A

26466883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85250393-C-G

http://identifiers.org/hco/21/GRCh38#26466920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85250425-C-A

26466920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85250425-C-T

26466924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85250428-T-G

26466946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85250449-A-G

26466980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85250485-T-C

26467428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85250913-A-T

http://identifiers.org/hco/21/GRCh38#26467836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85251219-C-A

26467878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85251246-T-C

26467962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85253934-T-C

http://identifiers.org/hco/21/GRCh38#26467991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85253962-C-A

26467991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85253962-C-T

26468067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85254039-A-G

26468069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85254041-G-T

26468130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85254098-A-G

http://identifiers.org/hco/21/GRCh38#26468146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85254114-C-A

26468146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85254114-C-T

http://identifiers.org/hco/21/GRCh38#26468167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85254123-C-A

http://identifiers.org/hco/21/GRCh38#26468168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85254124-C-A

26468168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85254124-C-G

26468170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85254126-G-T

http://identifiers.org/hco/21/GRCh38#26468197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85254153-A-C

26468197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85254153-A-G

26468230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85254185-T-C

http://identifiers.org/hco/21/GRCh38#26468302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85254257-C-A

http://identifiers.org/hco/21/GRCh38#26468314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85254268-C-A

26468314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85254268-C-T

26468362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85254304-G-T

26468438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85254373-A-G

26468438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85254373-A-T

26468534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85254469-T-G

26468621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85254556-G-C

26468930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85254860-A-G

http://identifiers.org/hco/21/GRCh38#26469118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85255619-A-C

26469119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85255620-G-C

26470746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 85256294-T-C

26470750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 85256297-G-T

http://identifiers.org/hco/21/GRCh38#26470801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85256347-C-A

26470801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85256347-C-T

26470815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85256361-A-G

26470815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85256361-A-T

26470817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85256363-G-T

26470856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85256401-A-G

26470857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85256402-A-T

26470944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85256483-A-G

26470966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85256505-G-C

26471030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85256528-G-A

26471049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85256543-C-T

26471127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85256621-A-T

http://identifiers.org/hco/21/GRCh38#26471184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85256676-C-A

26471184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85256676-C-T

26471232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85256741-T-A

26471232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85256741-T-C

26471359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85256867-G-A

26471493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85257026-G-A

26471493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85257026-G-T

26471655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85257177-T-A

26471655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85257177-T-C

26471753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85257279-T-G

26475776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85260550-C-T

26475791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85260573-T-C

26475808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85260592-G-A

26479456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85261781-G-A

26479614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85261936-T-C

http://identifiers.org/hco/21/GRCh38#26479960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85262130-C-A

http://identifiers.org/hco/21/GRCh38#26480032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85262202-C-A

http://identifiers.org/hco/21/GRCh38#26480235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85262384-C-A

26480235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85262384-C-T

26480491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85262707-T-C

http://identifiers.org/hco/21/GRCh38#26480526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85262743-C-A

26480526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85262743-C-T

26480617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85262853-G-C

26480729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85263061-C-T

http://identifiers.org/hco/21/GRCh38#26480956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85263292-C-A

http://identifiers.org/hco/21/GRCh38#26480977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85263313-C-A

26480981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85263317-T-G

26481014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85263379-A-G

26481852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85263716-T-A

26481857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85263721-A-G

26481860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85263723-A-T

http://identifiers.org/hco/21/GRCh38#26481900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85263769-C-A

26481900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85263769-C-T

http://identifiers.org/hco/21/GRCh38#26481964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85263840-A-C

26481968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85263844-A-G

26482053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85263932-C-T

26482085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85263953-G-T

26482143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85263999-A-T

26482173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85264029-C-T

26482189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85264045-A-T

26482336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85264173-A-G

26482372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85264208-T-C

26482424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85264260-A-G

http://identifiers.org/hco/21/GRCh38#26482633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85264403-C-A

26482641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85264411-G-T

26482826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85264952-C-T

26482841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85264967-T-C

26482993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85265098-C-T

26483016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85265118-C-G

26483155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85265327-A-T

26483305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85265503-G-A

26483305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85265503-G-T

26483317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85265514-C-T

http://identifiers.org/hco/21/GRCh38#26483353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85265547-A-C

26483353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85265547-A-G

26483353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85265547-A-T

http://identifiers.org/hco/21/GRCh38#26483417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85265610-A-C

26483429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85265620-G-A

26483429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85265620-G-T

26483434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85265625-A-G

26483436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85265627-G-T

26483438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85265629-A-G

http://identifiers.org/hco/21/GRCh38#26483442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85265633-A-C

http://identifiers.org/hco/21/GRCh38#26483461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85265652-A-C

http://identifiers.org/hco/21/GRCh38#26483521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85265697-C-A

26483521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85265697-C-G

26483675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85265858-C-T

26483962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85266059-T-C

26483989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85266086-T-C

26484013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85266107-A-G

26484072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85266153-T-G

26484182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85266229-T-G

http://identifiers.org/hco/21/GRCh38#26484206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85266253-A-C

26484244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85266290-A-G

26484308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85266353-G-A

26484462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85266524-G-A

26484701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85266764-T-A

26484712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85266775-T-C

26484718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85266781-G-T

26484786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85266852-T-A

http://identifiers.org/hco/21/GRCh38#26484842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85266906-C-A

26484842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85266906-C-T

http://identifiers.org/hco/21/GRCh38#26485114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85267170-C-A

26485134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85267193-A-G

26485134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85267193-A-T

26485270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85267327-G-T

26485288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85267345-A-G

26485375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85267435-G-A

26485397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85267457-C-T

26486693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85269435-A-T

26486849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85269602-G-A

26486905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85269652-G-A

26486911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85269654-G-A

26487239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85270475-A-T

26487310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85270540-C-T

26487333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85270563-A-G

http://identifiers.org/hco/21/GRCh38#26487516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85270750-C-A

26487782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85271242-G-A

26487880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85271330-A-T

26487882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85271332-C-T

26491541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85271563-G-A

26491615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85271637-G-T

26492023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85271974-T-C

26492038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85271989-C-T

26492276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85272269-G-A

26492280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85272273-T-C

26492318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85272319-C-T

26492339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85272340-T-G

26492391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85272395-T-A

http://identifiers.org/hco/21/GRCh38#26492481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85272481-C-A

26492481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85272481-C-T

26493337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85272639-A-G

26493877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85273191-C-T

26493973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85273283-A-G

26494075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85273383-G-A

26494129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85273435-C-T

26494194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85273500-A-T

26494697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85274136-G-T

26494778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85274215-A-G

26495205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85274602-T-G

26495214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85274611-C-G

26495247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85274642-T-C

http://identifiers.org/hco/21/GRCh38#26496409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85276455-A-C

http://identifiers.org/hco/21/GRCh38#26496513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85276329-C-A

http://identifiers.org/hco/21/GRCh38#26496677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85276063-A-C

26497401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85275552-T-C

26497618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85276888-T-C

26497862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85277047-C-G

26497890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85277067-A-G

26498054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85277233-C-T

26498188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85277343-A-G

26498388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85277456-C-T

26499030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85277710-G-A

http://identifiers.org/hco/21/GRCh38#26499054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85277736-A-C

26499146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85277859-C-G

26499311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85278090-G-A

26499311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85278090-G-T

26499458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85278226-C-T

26499465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85278233-G-A

26499747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85278476-C-T

26499807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85278537-G-A

26499872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85278587-A-G

26499872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85278587-A-T

http://identifiers.org/hco/21/GRCh38#26499887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85278602-C-A

26499887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85278602-C-T

26499916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85278628-A-G

26499954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85278665-G-A

26500037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85278745-A-G

26500186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85278863-C-T

26500193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85278870-T-G

26500218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85278887-A-G

26500424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85279079-T-C

26500443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85279096-G-C

26500447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85279100-A-G

26500494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85279140-G-A

26500571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85279199-C-T

26500803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85279386-A-G

26500900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85279512-A-G

26500901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85279513-G-A

26501331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85279642-G-A

26501421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85279706-T-A

26501421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85279706-T-C

26501492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85279780-A-G

26501529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85279818-C-T

26501621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85279903-C-T

26501673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85279956-T-C

26501687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85279972-A-T

26501688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85279973-T-C

26501718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85280001-T-A

26501988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85280324-A-G

26502168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85280497-T-C

26502771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85280739-G-A

26502824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85280790-T-C

26502866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85280830-T-C

26503045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85281009-C-T

26503171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85281142-C-T

26503249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85281234-A-T

26503399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85281369-T-C

http://identifiers.org/hco/21/GRCh38#26503466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85281431-A-C

26503491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85281456-C-T

26503517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85281543-T-C

26503524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85281550-G-T

26503630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85281667-T-A

26503688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85281703-T-A

26503710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 85281730-A-T

26503778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85281802-A-G

http://identifiers.org/hco/21/GRCh38#26503834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85281866-A-C

26503931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85281973-T-C

26503986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85282034-C-T

26504004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85282052-C-G

26504045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85282101-T-A

http://identifiers.org/hco/21/GRCh38#26505232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85282412-C-A

26505285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85282475-A-G

26505377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85282562-G-A

26505487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85282663-G-A

26505577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85282766-G-C

http://identifiers.org/hco/21/GRCh38#26505797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85282991-C-A

26505806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85283000-A-T

26505830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85283026-C-T

26505836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85283032-C-T

26505860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85283054-G-A

http://identifiers.org/hco/21/GRCh38#26505945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85283174-C-A

26505945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85283174-C-T

26506136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85283334-T-C

http://identifiers.org/hco/21/GRCh38#26506210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85283411-A-C

26506263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85283472-C-T

26506324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85283518-G-A

26506340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85283533-G-A

26506340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85283533-G-C

26506462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85283653-G-T

http://identifiers.org/hco/21/GRCh38#26506543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85283739-C-A

26506543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85283739-C-T

26506574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85283767-G-T

http://identifiers.org/hco/21/GRCh38#26506588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85283781-C-A

26506609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85283794-G-A

26506609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85283794-G-T

http://identifiers.org/hco/21/GRCh38#26506671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85283832-C-A

26506671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85283832-C-T

26506748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85283914-G-A

26506753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85283919-T-C

26506823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85283976-G-A

26506823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85283976-G-T

http://identifiers.org/hco/21/GRCh38#26506845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85283997-C-A

26506904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85284056-T-A

26506904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85284056-T-C

26506948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85284083-C-G

26506956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85284087-A-G

26507017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85284153-A-G

26507069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85284204-T-A

26507069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85284204-T-C

26507438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85284522-A-T

26507443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85284526-G-A

26507462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85284544-A-T

26507666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85284728-A-G

26507668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85284730-G-A

26507810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85284891-G-T

26507892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85284980-T-C

26508072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85285129-A-G

26508111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85285168-A-G

26508161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85285220-T-A

26508334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85285427-A-G

26508361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85285454-G-A

26508385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85285477-A-G

26508409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85285501-T-A

http://identifiers.org/hco/21/GRCh38#26508664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85285687-C-A

26508880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85285877-T-C

26508907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85285902-A-T

http://identifiers.org/hco/21/GRCh38#26508934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85285935-C-A

26510456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85287937-G-A

26510481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85287974-A-G

26510543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85288087-T-C

26510720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85288262-C-G

26510920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85288465-G-A

26511178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85288830-A-G

26511263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85288907-C-G

26511305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85288948-A-G

26511442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85289081-A-G

26511555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85289188-T-C

26511580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85289212-G-A

26511589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85289221-A-G

26511677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85289302-G-A

26511677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85289302-G-C

26511677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85289302-G-T

26511859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85289541-G-A

26511896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85289578-G-C

http://identifiers.org/hco/21/GRCh38#26511974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85289673-A-C

26512528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85289855-G-A

26512528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85289855-G-T

26512534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85289861-T-A

26512554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85289883-C-T

26512604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85289929-A-G

26512626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85289951-G-A

26512721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85290043-A-G

26512963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85290274-A-T

26513011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85290324-T-C

26513220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85290517-C-G

26513247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85290544-T-C

http://identifiers.org/hco/21/GRCh38#26513400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85290696-C-A

26513484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85290777-C-G

26514998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85291412-A-G

26515106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85291526-C-G

http://identifiers.org/hco/21/GRCh38#26515161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85291707-C-A

26515204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85291749-C-T

26515621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85291862-C-T

http://identifiers.org/hco/21/GRCh38#26516736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85293459-A-C

http://identifiers.org/hco/21/GRCh38#26516763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85293485-C-A

26517247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85293643-G-A

26517247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85293643-G-C

26517531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85293919-G-A

26523924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85296791-C-T

26523979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85296850-G-A

26524010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85296874-C-G

http://identifiers.org/hco/21/GRCh38#26524307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85297042-A-C

26524452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85297160-G-T

26525784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85299251-G-T

26526662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85299465-T-G

26526736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85299535-A-T

26527195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85300028-G-A

26527206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85300046-T-A

26527206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85300046-T-G

http://identifiers.org/hco/21/GRCh38#26527219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85300069-C-A

26527219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85300069-C-G

26527979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85300954-A-T

26528006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85300990-C-T

26528012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85300996-A-G

26528014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85300998-G-A

26528890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85301429-A-T

26528928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85301470-C-G

http://identifiers.org/hco/21/GRCh38#26529167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85301716-C-A

26529241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85301798-T-C

26529242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85301799-T-C

26529263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85301822-A-G

http://identifiers.org/hco/21/GRCh38#26529372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85301902-A-C

26529374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85301904-A-G

26529390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85301920-G-A

26533293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85302838-G-A

26533293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85302838-G-C

26533294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85302839-G-A

http://identifiers.org/hco/21/GRCh38#26533334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85302872-C-A

26533334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85302872-C-T

26533365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85302905-T-A

26533400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85302938-C-G

26533568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85303106-A-G

26533593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85303131-C-T

26533799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85303400-G-C

26533827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85303418-A-G

26533853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85303444-C-T

26534021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85303810-C-T

26536295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85304132-T-C

26536409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85304242-G-T

26536462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85304303-C-G

26536553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85304390-C-G

26536599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85304434-G-A

http://identifiers.org/hco/21/GRCh38#26537347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85305949-A-C

26537384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85305986-T-C

26537386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85305988-G-A

26537499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85306096-T-C

26538010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85307376-T-C

26538170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85307549-C-T

26538362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85307714-A-G

26538976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85308433-T-G

26539327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85308750-T-A

26539679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85309089-T-C

26539749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85309159-G-A

26539765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85309175-G-C

26539765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85309175-G-T

26540119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85309516-C-T

26540129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85309535-T-C

26540193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85309599-C-G

26540193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85309599-C-T

26544231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85313508-T-G

26544254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85313534-T-C

26544256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85313536-C-G

26544256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85313536-C-T

26544369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85313645-A-G

26544536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85313798-G-A

26544538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85313800-T-G

26544661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85313913-T-C

26545325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85314990-C-G

26545517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85315111-C-T

26545519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85315113-G-A

http://identifiers.org/hco/21/GRCh38#26547973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85316054-C-A

26547983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85316063-T-G

26548000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85316079-G-A

26548000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85316079-G-T

26548650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85316401-G-C

26548650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85316401-G-T

26548885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85316632-C-T

26548965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85316719-G-A

26549017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85316760-G-A

26549041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85316784-G-A

26549247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85316990-G-C

26549262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85317005-A-G

26549410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85317166-C-G

26549410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85317166-C-T

26554086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85324707-C-T

26554221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85324842-A-G

26554317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85324994-G-A

26554317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85324994-G-T

26554633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85325330-C-T

26554758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85325439-T-C

26555145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85325713-C-T

26555298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85332514-T-C

26555372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85332589-A-G

26555389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85332606-A-G

26555448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85332664-T-C

26555467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85332682-G-A

26555513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85332727-T-G

26555531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85332745-G-T

26555631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85332847-G-A

26555752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85332965-T-A

http://identifiers.org/hco/21/GRCh38#26555760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85332973-A-C

26555772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85332985-T-C

26555835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85333048-T-A

26555840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85333053-G-T

26555968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85333185-C-G

26555969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85333186-A-G

26556078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85333289-A-G

26560723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85336500-T-C

26560824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85336620-T-A

26560910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85336698-T-C

26561381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85337540-C-T

26561491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85337631-C-T

26561883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85338003-G-A

26561917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85338037-G-A

26561985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85338106-T-C

26562030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85338150-G-T

26562046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85338166-C-T

26562263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85338398-T-C

http://identifiers.org/hco/21/GRCh38#26562336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85338498-C-A

26562336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85338498-C-G

26562556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85338705-T-C

http://identifiers.org/hco/21/GRCh38#26562715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85338869-C-A

26562715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85338869-C-T

26563795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85339019-C-T

26563862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85339106-T-C

26564560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85339883-G-T

26564784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85340103-T-A

26564784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85340103-T-C

26564784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85340103-T-G

http://identifiers.org/hco/21/GRCh38#26564816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85340136-A-C

26564816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85340136-A-T

http://identifiers.org/hco/21/GRCh38#26564946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85340257-C-A

26564946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85340257-C-T

26565197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85340500-A-G

26565214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85340517-T-A

26565214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85340517-T-C

26565232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85340535-G-A

26565234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85340537-G-A

26565405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85340731-T-C

26565464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85340785-T-C

26565619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85340961-C-T

26565672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85341016-C-T

26565781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85341097-T-C

http://identifiers.org/hco/21/GRCh38#26566143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85341438-C-A

26566143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85341438-C-T

26566190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85341644-G-T

26566194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85341648-T-A

26566238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85341681-A-T

26566239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85341682-G-A

26566239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85341682-G-T

26566242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85341685-T-C

26566249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85341692-A-G

26566335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85341778-T-C

26566394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85341832-C-G

26566394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85341832-C-T

http://identifiers.org/hco/21/GRCh38#26566434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85341872-C-A

26566437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85341874-T-C

26566471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85341905-G-T

http://identifiers.org/hco/21/GRCh38#26566527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85341977-A-C

26566593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85342032-C-G

26566593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85342032-C-T

26567126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85342257-A-G

26567236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85342364-T-G

26567361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85342472-T-C

26567400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85342515-A-T

26567584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85342729-G-A

26567584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85342729-G-C

26567631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85342772-T-C

26567890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85343013-G-A

26567890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85343013-G-T

http://identifiers.org/hco/21/GRCh38#26567980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85343102-C-A

26567984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85343106-C-T

26568013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85343121-G-A

http://identifiers.org/hco/21/GRCh38#26568014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85343122-C-A

26568014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85343122-C-G

26568014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85343122-C-T

26568122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85343202-T-C

26568129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85343209-T-C

26568219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85343439-T-C

26568271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85343491-G-T