72956207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98951522-G-C

72956274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, undefined
orthologous variants: 98951454-G-A

72956274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, undefined
orthologous variants: 98951454-G-C

72956488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98951284-A-T

72956611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98951239-C-G

72956708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98951142-C-T

72957104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98950847-A-G

72957187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98950776-T-C

http://identifiers.org/hco/5/GRCh38#72957533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98950492-C-A

72957802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98950185-T-C

72957947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98950063-A-T

72959714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98947017-A-G

72960192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98946897-A-T

72961127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98946103-A-G

72961190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98946039-A-G

72961276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98945961-T-C

72961435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98945619-C-G

72961435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98945619-C-T

72966489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98944581-A-G

72966827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98944275-T-C

72968407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98942983-A-G

72968407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98942983-A-T

http://identifiers.org/hco/5/GRCh38#72968450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98942942-C-A

72968608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98942796-A-T

http://identifiers.org/hco/5/GRCh38#72968666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98942745-A-C

72968666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98942745-A-G

72968683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98942726-G-T

72968887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98942359-A-G

72969174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98941587-G-C

72969292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98941467-G-T

72969480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98941271-C-T

72969482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98941269-C-G

72969482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98941269-C-T

72969698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98941088-G-A

72969698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98941088-G-T

72987827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98934827-C-T

72989571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98932729-G-A

72989571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98932729-G-C

http://identifiers.org/hco/5/GRCh38#72989642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98932664-C-A

72989642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98932664-C-T

72990302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98926545-A-G

72990431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98926427-T-A

72990454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98926404-T-C

72990632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98926225-T-C

72990686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98926145-T-C

72990687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98926144-T-C

72990688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98926143-G-C

72990694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98926039-T-A

72990745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense variant
orthologous variants: 98925988-G-A

72990745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense variant
orthologous variants: 98925988-G-T

72990772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense variant
orthologous variants: 98925961-G-A

72990772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense variant
orthologous variants: 98925961-G-T

72990796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense variant
orthologous variants: 98925937-T-A

72991643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98925171-C-T

http://identifiers.org/hco/5/GRCh38#73004547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98923763-A-C

73004917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98923462-A-G

73004917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98923462-A-T

73005086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98923263-G-C

73005590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98922754-A-G

73005621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98922723-G-A

73005768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98922481-G-T

73005838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98922381-T-C

73006057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98922004-C-T

73006075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98921985-A-G

73006264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98921736-G-T

http://identifiers.org/hco/5/GRCh38#73006385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98921621-C-A

73006385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98921621-C-G

73006385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98921621-C-T

73006408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98921431-T-A

73006478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, missense_variant
orthologous variants: 98921353-T-C

73006517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, missense_variant
orthologous variants: 98921314-G-A

73006517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, missense_variant
orthologous variants: 98921314-G-T

http://identifiers.org/hco/5/GRCh38#73006562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98921268-A-C

73006562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98921268-A-G

73006941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98920563-C-T

73007345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98920245-T-A

73007566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98920041-G-A

73007886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98919742-G-A

73007994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98919548-G-A

73013097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98915012-A-T

73013236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98914900-C-T

73013282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98914859-C-G

73013282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98914859-C-T

73015132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98914176-G-A

73015665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, missense_variant
orthologous variants: 98913954-A-G

http://identifiers.org/hco/5/GRCh38#73015707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98913912-C-A

73016045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98912803-A-G

73017034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98912576-T-A

73017043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98912567-C-T

73017113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98912515-A-G

73017474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98911864-G-A

73017966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98911037-C-T

73018254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98910658-A-G

73031598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98905578-A-G

73031954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98905238-C-G

73032094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, undefined
orthologous variants: 98905076-G-A

73032094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, undefined
orthologous variants: 98905076-G-C

73032094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, undefined
orthologous variants: 98905076-G-T

73032891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98904388-T-C

73032982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98904307-A-G

73033244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98904064-T-C

73033304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98904001-G-T

73033725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98903227-T-C

73034037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98902575-T-C

73034110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98902503-A-T

73034421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98902228-T-A

73034692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98901020-G-A

http://identifiers.org/hco/5/GRCh38#73034760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98900959-C-A

73034765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98900954-A-G

73034777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98900942-G-A

73034777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98900942-G-C

73037362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98900046-A-G

73041439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98899223-A-G

73041496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98899167-A-G

73041520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98899144-A-G

73041603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98899066-T-A

73042029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98898549-C-T

http://identifiers.org/hco/5/GRCh38#73042043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98898535-A-C

http://identifiers.org/hco/5/GRCh38#73042135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98898449-A-C

http://identifiers.org/hco/5/GRCh38#73042330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98897747-A-C

73044836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98895400-T-C

73044967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98895282-T-C

73045352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98894925-A-G

73045369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98894913-A-T

73045701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98894627-C-T

http://identifiers.org/hco/5/GRCh38#73051075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98892515-C-A

73051090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98892500-T-A

73051106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98892484-A-G

73051153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98892469-A-G

73051230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98892428-A-G

73051230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98892428-A-T

73051254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98892403-T-C

73051254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98892403-T-G

73051289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98892192-A-G

73051300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98892181-T-G

73051322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98892159-T-A

73051322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98892159-T-C

73051376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98892104-T-A

73051376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98892104-T-C

73051426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98892055-T-G

73051482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98891996-A-G

73051509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98891974-A-G

http://identifiers.org/hco/5/GRCh38#73052415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98891678-C-A

73052431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98891662-A-G

73052461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98891632-A-G

73052508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: non_coding_transcript_exon_variant, splice_donor_variant
orthologous variants: 98891585-G-A

73052508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: non_coding_transcript_exon_variant, splice_donor_variant
orthologous variants: 98891585-G-C

73052508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: non_coding_transcript_exon_variant, splice_donor_variant
orthologous variants: 98891585-G-T

73052522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98891563-G-A

73052522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98891563-G-T

73052534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98891551-T-G

73052623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98890833-G-A

73052623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98890833-G-C

73052623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98890833-G-T

73052677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98890779-T-C

73053798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98889200-T-G

73054081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98888933-G-A

73054081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98888933-G-C

73054176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98888835-G-A

73054176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98888835-G-T

73054217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98888795-T-C

73054352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98888634-T-C

http://identifiers.org/hco/5/GRCh38#73054502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98888461-C-A

73054502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98888461-C-T

73054504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98888459-T-C

73054557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 98888405-T-C

73054666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98888301-G-A

73054666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98888301-G-C

73054666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98888301-G-T

73054702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98888270-A-G

73054702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98888270-A-T

73054753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98888226-A-G

73055014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98887977-T-C

http://identifiers.org/hco/5/GRCh38#73055114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98887307-C-A

73055114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98887307-C-T

73055917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98886576-C-T

73056224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98886234-T-C

http://identifiers.org/hco/5/GRCh38#73056231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98886227-C-A

73056231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98886227-C-T

73056250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98886212-A-G

73056455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98885964-C-T

73056708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98885715-A-G

73056713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98885709-T-C

http://identifiers.org/hco/5/GRCh38#73056750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98885679-C-A

73056750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98885679-C-T

73056857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98885562-G-A

73058422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98884821-T-C

73058425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 98884818-T-A

73058425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 98884818-T-C

http://identifiers.org/hco/5/GRCh38#73058476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98884767-C-A

73058476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98884767-C-T

73058503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98884743-T-C

73058534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98884692-T-A

73058534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98884692-T-C

73058546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98884680-T-C

73062307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98884383-A-G

73062560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98884109-T-G

http://identifiers.org/hco/5/GRCh38#73062769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98883911-C-A

73062929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98883782-T-C

73063254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98882956-T-G

73063474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98882766-C-T

73063541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98882699-T-C

73063724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98882507-G-A

73063724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98882507-G-T

http://identifiers.org/hco/5/GRCh38#73063738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98882493-A-C

73063738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98882493-A-G

73063806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98882444-G-T

http://identifiers.org/hco/5/GRCh38#73063952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98882299-C-A

73064352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98881770-A-G

73065101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98880996-A-G

73068418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98880254-G-T

73068468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98880206-T-A

73068614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98880081-T-C

73068669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98880027-C-G

73068669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98880027-C-T

73068716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98879980-G-A

73068815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98879885-T-C

73068815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98879885-T-G

http://identifiers.org/hco/5/GRCh38#73068877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98879417-C-A

73068877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98879417-C-T

http://identifiers.org/hco/5/GRCh38#73070337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98877652-A-C

73070564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98877433-G-A

73070564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98877433-G-T

http://identifiers.org/hco/5/GRCh38#73070633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98877278-A-C

73070943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 98876975-G-A

73074759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98871619-A-G

73074907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98871481-A-G

73077228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98869298-A-G

73077236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98869290-G-A

73077236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98869290-G-T

http://identifiers.org/hco/5/GRCh38#73077259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98869267-C-A

73077259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98869267-C-T

73077260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98869266-G-A

73077260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98869266-G-T

http://identifiers.org/hco/5/GRCh38#73077411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98869106-C-A

73077414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98869103-A-G

73077414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98869103-A-T

73077792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98869012-G-A

http://identifiers.org/hco/5/GRCh38#73078042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98868836-C-A

73078125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98868761-G-A

73078163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98868732-A-G

73078163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98868732-A-T

73078325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98868570-A-T

73078355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98868540-A-G

73078363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98868532-A-G

http://identifiers.org/hco/5/GRCh38#73078366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98868529-C-A

73078366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98868529-C-G

73078366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98868529-C-T

73078405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98868487-T-C

73078414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98868478-A-G

73078538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98868365-T-C

73078612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98868298-A-G

73078631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98868285-G-A

http://identifiers.org/hco/5/GRCh38#73081370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98867861-C-A

73081544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98867679-C-G

http://identifiers.org/hco/5/GRCh38#73081572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98867665-C-A

73081630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98867630-C-T

73081645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98867615-G-A

73081645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98867615-G-T

http://identifiers.org/hco/5/GRCh38#73081646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98867614-C-A

73081646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98867614-C-T

73081682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98867582-T-A

73081682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98867582-T-C

http://identifiers.org/hco/5/GRCh38#73081716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98867548-C-A

73081716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98867548-C-T

http://identifiers.org/hco/5/GRCh38#73081721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98867543-C-A

73081721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98867543-C-T

http://identifiers.org/hco/5/GRCh38#73081728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98867536-A-C

73081728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98867536-A-G

73081816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense variant
orthologous variants: 98867449-A-G

73081963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense variant
orthologous variants: 98867302-T-C

http://identifiers.org/hco/5/GRCh38#73082009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98867262-C-A

73082009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98867262-C-T

73082674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98866839-T-G

73082780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: missense variant
orthologous variants: 98866740-G-A

http://identifiers.org/hco/5/GRCh38#73082961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98866655-C-A

73082961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98866655-C-T

73083054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98866577-G-T

73083184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98866490-A-G

73083196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98866479-T-G

73083483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98866214-T-G

73084576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98865822-T-C

73084717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98865691-T-C

73085007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98865431-G-C

73086215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98865158-G-C

73086221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98865152-T-C

73086270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98865096-T-C

http://identifiers.org/hco/5/GRCh38#73086594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98864597-C-A

73086646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98864540-T-A

http://identifiers.org/hco/5/GRCh38#73087153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98863527-A-C

73087219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98863459-A-G

73087331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98863328-G-T

73087554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98862766-T-C

http://identifiers.org/hco/5/GRCh38#73087855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98862501-A-C

http://identifiers.org/hco/5/GRCh38#73087965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98862386-A-C

73087965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98862386-A-G

73087988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: intron variant
orthologous variants: 98862363-T-C

73088140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: 3 prime UTR variant
orthologous variants: 98862209-G-T

73088316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: 3 prime UTR variant
orthologous variants: 98862038-A-G

73088317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: 3 prime UTR variant
orthologous variants: 98862037-T-G

http://identifiers.org/hco/5/GRCh38#73088343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98862012-A-C

http://identifiers.org/hco/5/GRCh38#73088463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#98861911-C-A

73088463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: 3 prime UTR variant
orthologous variants: 98861911-C-G

73088463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: 3 prime UTR variant
orthologous variants: 98861911-C-T

73089111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: 3 prime UTR variant
orthologous variants: 98861261-G-A

73089139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: 3 prime UTR variant
orthologous variants: 98861233-T-C

73089301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: 3 prime UTR variant
orthologous variants: 98861085-G-A

73089301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: 3 prime UTR variant
orthologous variants: 98861085-G-T

73090476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25180
most severe consequence: 3 prime UTR variant
orthologous variants: 98859958-T-C