241017449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93179476-C-G

241017449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93179476-C-T

241017616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93179644-C-G

241029659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93183593-G-A

http://identifiers.org/hco/2/GRCh38#241030145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93183855-C-A

241030145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93183855-C-T

http://identifiers.org/hco/2/GRCh38#241030331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#93184034-C-A

241030331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93184034-C-G

http://identifiers.org/hco/2/GRCh38#241030618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93184324-C-A

241030693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93184368-G-T

http://identifiers.org/hco/2/GRCh38#241031567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93185450-C-A

http://identifiers.org/hco/2/GRCh38#241032693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93185832-C-A

241033298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93186351-T-C

241033490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93186523-G-T

241033551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93186570-G-A

241033551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93186570-G-C

241033551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93186570-G-T

241033595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93186607-C-T

241033698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93186650-G-A

241033722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93186676-C-G

241033722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93186676-C-T

241033730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 93186683-G-A

241033730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 93186683-G-C

241033803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93186756-C-T

http://identifiers.org/hco/2/GRCh38#241033887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93186842-C-A

241033887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93186842-C-T

http://identifiers.org/hco/2/GRCh38#241033905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93186860-C-A

241033905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93186860-C-G

241033905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93186860-C-T

241033939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93186893-G-A

241033939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93186893-G-T

241033960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93186914-G-A

241033960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93186914-G-T

241033996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93186958-G-A

241033996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93186958-G-T

241034025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93186994-G-A

241034025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93186994-G-T

241034107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93187022-G-T

241034113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93187028-C-G

241034466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93187225-A-G

http://identifiers.org/hco/2/GRCh38#241034482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93187241-C-A

241034482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93187241-C-G

241034482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93187241-C-T

241034770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93187556-G-T

241036464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93189014-G-A

241036621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93189199-G-A

241036712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93189287-G-A

241036720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93189295-G-A

241036720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93189295-G-C

241036720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93189295-G-T

241036721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93189296-G-A

241036848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93189429-C-T

241036869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93189450-C-T

241036938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93189521-G-T

241036942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93189558-A-T

http://identifiers.org/hco/2/GRCh38#241037032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93189638-C-A

241037032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93189638-C-G

241037067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93189659-G-A

241037119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93189708-T-A

241037310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93189896-C-T

241037325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93189911-T-C

241037352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 93189938-A-G

241037528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93190062-A-G

241037617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93190154-C-T

241037895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93190349-G-C

241038060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93190503-G-A

241038108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93190547-T-A

http://identifiers.org/hco/2/GRCh38#241040000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93192684-C-A

241040000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93192684-C-T

241040001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93192685-G-A

241040001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93192685-G-T

241040002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93192686-T-C

http://identifiers.org/hco/2/GRCh38#241040018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93192702-C-A

241040018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 93192702-C-T

241040025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93192709-G-A

241040079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93192764-A-G

http://identifiers.org/hco/2/GRCh38#241040115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#93192800-C-A

241040115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93192800-C-T

241040145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93192830-G-A

241040145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93192830-G-T

http://identifiers.org/hco/2/GRCh38#241040166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#93192851-C-A

241040166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93192851-C-T

241040485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93193166-T-C

241040640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93193242-C-T

241040801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93193382-A-G

241040888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 93193482-G-A

http://identifiers.org/hco/2/GRCh38#241040892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#93193486-C-A

241040898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93193492-A-G

241041324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93194051-G-T

241041411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93194142-G-A

241041411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93194142-G-T

241041413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93194144-G-A

241041413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93194144-G-T

241041421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93194150-A-G

http://identifiers.org/hco/2/GRCh38#241041432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93194160-C-A

241042261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93194761-C-T

241042743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93195009-C-T

241043190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93195258-G-A

241046732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93197653-A-G

241046832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93197755-A-T

241046850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93197773-A-G

241046978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93197899-A-G

241047170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93198073-G-A

241047170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93198073-G-T

241047675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93198463-C-G

241048143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93198692-C-T

241048295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93198844-G-T

241048333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93198882-A-G

http://identifiers.org/hco/2/GRCh38#241048334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#93198883-C-A

241048334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93198883-C-T

241048394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93198943-C-T

http://identifiers.org/hco/2/GRCh38#241048452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93199001-C-A

http://identifiers.org/hco/2/GRCh38#241048580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93199216-C-A

241048580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93199216-C-G

241048580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93199216-C-T

241048583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93199219-G-A

241048583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93199219-G-T

241048591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93199235-G-A

241048635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93199299-G-A

241048662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 93199321-G-A

241048662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 93199321-G-T

241048691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93199350-G-A

http://identifiers.org/hco/2/GRCh38#241048798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93199444-C-A

241048798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93199444-C-T

http://identifiers.org/hco/2/GRCh38#241048929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93199491-A-C

241048940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93199502-G-A

241049053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93199608-A-G

241049272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93199776-T-C

http://identifiers.org/hco/2/GRCh38#241049335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93199827-A-C

241049717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93200153-A-T

241049778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93200176-G-A

241049787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93200185-C-T

241049810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 93200207-C-G

241049810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 93200207-C-T

241049881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93200278-C-T

http://identifiers.org/hco/2/GRCh38#241049945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#93200395-A-C

http://identifiers.org/hco/2/GRCh38#241049994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#93200455-C-A

241049994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93200455-C-G

241049994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93200455-C-T

http://identifiers.org/hco/2/GRCh38#241050001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#93200460-C-A

241050001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93200460-C-T

241050002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93200461-T-C

241050080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93200528-G-T

241050113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93200564-G-T

http://identifiers.org/hco/2/GRCh38#241051180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93201356-C-A

http://identifiers.org/hco/2/GRCh38#241051357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93201448-C-A

241051596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93201608-G-A

241051596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93201608-G-T

241051658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93201683-G-A

241051658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93201683-G-T

http://identifiers.org/hco/2/GRCh38#241051711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93201736-C-A

241051711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93201736-C-T

http://identifiers.org/hco/2/GRCh38#241051713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93201739-C-A

241051713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93201739-C-G

241051713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93201739-C-T

http://identifiers.org/hco/2/GRCh38#241051808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#93201835-C-A

241051808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93201835-C-T

241052010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93202028-G-A

241052010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93202028-G-T

241052270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93202270-G-T

241052321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93202292-A-T

241053034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93202930-A-T

241053109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93202985-A-G

241053224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93203090-G-A

241053224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93203090-G-C

241053261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93203127-G-T

http://identifiers.org/hco/2/GRCh38#241053317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#93203183-C-A

241053317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93203183-C-G

http://identifiers.org/hco/2/GRCh38#241053456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93203287-C-A

241053456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93203287-C-T

http://identifiers.org/hco/2/GRCh38#241053464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93203295-C-A

241053464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93203295-C-T

241053595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93203423-A-G

241053595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93203423-A-T

241053906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93203685-C-T

241053984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93203751-T-C

241054079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93203829-G-A

241054327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93204059-G-A

241055450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93204484-T-C

241055804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93204841-A-T

241055954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93204978-C-T

241056014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93205039-C-T

241056044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93205069-G-A

241056083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93205108-G-A

241062558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93208010-G-C

241062611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93208064-T-C

http://identifiers.org/hco/2/GRCh38#241062657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93208082-C-A

241062657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93208082-C-T

241062699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93208111-A-T

http://identifiers.org/hco/2/GRCh38#241062788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93208200-C-A

241062806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93208218-G-A

241062806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93208218-G-C

241062806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93208218-G-T

241062854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93208266-G-A

241062854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93208266-G-T

http://identifiers.org/hco/2/GRCh38#241062921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93208333-C-A

241062921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93208333-C-T

241062929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93208341-G-A

241062929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93208341-G-C

241062929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93208341-G-T

241063048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93208438-T-G

http://identifiers.org/hco/2/GRCh38#241063269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93208662-C-A

241063269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93208662-C-G

241063435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93208811-G-C

241063435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93208811-G-T

http://identifiers.org/hco/2/GRCh38#241063469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93208844-A-C

241063469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93208844-A-G

241063469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93208844-A-T

http://identifiers.org/hco/2/GRCh38#241063569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93208941-C-A

241063707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 93209078-G-A

http://identifiers.org/hco/2/GRCh38#241063796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93209156-C-A

241063796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93209156-C-G

http://identifiers.org/hco/2/GRCh38#241063800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93209160-C-A

241063800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93209160-C-G

241063824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93209184-G-T