80263096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: non coding transcript exon variant
orthologous variants: 84168518-A-G

80264014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: non coding transcript exon variant
orthologous variants: 84168055-G-T

80264016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: non coding transcript exon variant
orthologous variants: 84168053-T-C

80264040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: non coding transcript exon variant
orthologous variants: 84168029-G-A

80267506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84163390-C-T

80267513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84163383-G-A

80267596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84163317-A-G

80267809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84163111-G-A

80267867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84163055-G-A

80267873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84163049-A-G

80267909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84163013-C-T

80267973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84162955-T-G

80268031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84162906-A-G

80268184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84162762-G-A

80268298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84162647-G-A

80268357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84162614-T-C

80268429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84162563-G-A

80268490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84162502-T-C

80270601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84155983-T-C

80270628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84155959-G-A

80270628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84155959-G-T

80270707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84155892-A-G

80270718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84155880-A-G

80275965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84154413-G-A

80276022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84154364-G-T

http://identifiers.org/hco/15/GRCh38#80276091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84154318-C-A

80276103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84154306-T-C

80276158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84154251-C-T

80276287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84154121-G-A

http://identifiers.org/hco/15/GRCh38#80276471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84153955-C-A

80276523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84153907-C-G

80278182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84152776-G-A

80278281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84152685-C-T

80278563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84152510-T-C

80278736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84152381-T-C

80278759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84152359-G-A

80279042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84152072-T-C

80279152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84151959-G-A

http://identifiers.org/hco/15/GRCh38#80279217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84151892-A-C

80279424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84151696-T-C

80279430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84151690-G-T

80279528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84151686-T-C

80279718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84151518-A-G

80279803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84151437-T-C

http://identifiers.org/hco/15/GRCh38#80279873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84151376-C-A

80279933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84151283-G-A

http://identifiers.org/hco/15/GRCh38#80279996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84151215-C-A

80279996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84151215-C-T

http://identifiers.org/hco/15/GRCh38#80280004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84151207-C-A

80280004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84151207-C-T

80280051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84151160-A-G

80280052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84151159-G-A

80280052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84151159-G-T

80280069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84151142-T-C

80280100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84151113-G-T

http://identifiers.org/hco/15/GRCh38#80280110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84151103-C-A

80280110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84151103-C-G

80280110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84151103-C-T

80280222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84151088-G-T

80280331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84151022-T-C

80280331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84151022-T-G

80280345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84151010-G-C

80280345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84151010-G-T

http://identifiers.org/hco/15/GRCh38#80280366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84150993-C-A

80280368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84150991-A-G

80280394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84150966-G-T

80283413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84149820-G-C

80283519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84149711-T-C

80283606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84149629-T-C

80283731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84149536-G-A

80283831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84149439-C-T

80283875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84149385-G-T

80284025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84149232-G-C

80284075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84149186-C-T

80284194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84149028-C-T

80284196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84149026-G-T

http://identifiers.org/hco/15/GRCh38#80284202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84149020-C-A

80284202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84149020-C-G

80284202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84149020-C-T

80284234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84148988-G-T

http://identifiers.org/hco/15/GRCh38#80284268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84148929-A-C

80284268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84148929-A-T

80284358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84148835-A-G

80284995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84148055-A-G

80284995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84148055-A-T

80285291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84147766-G-A

80285429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84147653-C-T

80285439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84147644-A-G

80285447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84147636-G-A

80285479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84147604-T-C

80285541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84147560-G-A

80285561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84147541-G-A

80285567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84147535-C-T

80285570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84147532-G-A

80285679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84147474-C-T

80286510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84138713-C-T

80286611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84138614-G-A

80286689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84138540-T-C

80286722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84138507-T-A

80286724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84138505-C-T

80286773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84138459-T-G

80286784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84138449-T-C

80287066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84138198-G-A

80287066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84138198-G-C

80287149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84138095-A-G

80287196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84138024-G-C

80287276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84137922-C-T

80287402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84137800-G-A

80287571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84137638-C-G

80287620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84137584-T-G

80287628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84137576-G-A

80287762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84137462-G-A

http://identifiers.org/hco/15/GRCh38#80287853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84137387-C-A

80288085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84136457-C-T

80288202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84136351-T-C

80288228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84136325-A-G

80288252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84136300-A-G

http://identifiers.org/hco/15/GRCh38#80288306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84136245-C-A

80288644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84136005-A-G

80288669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84135971-T-C

80288815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84135827-G-A

80290074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84134579-G-C

80290130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84134527-T-A

80290419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84134052-G-A

80290504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84133968-G-A

80290688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84133877-G-A

80290688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84133877-G-C

80290730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84133836-A-G

80290741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84133825-T-A

80290741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84133825-T-G

80290816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84133747-T-C

80291579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84133535-C-G

80291723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84133384-C-T

80292176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84132597-A-G

80292427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84132377-T-C

80292501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84132307-C-T

80292503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84132305-G-A

80292516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84132292-A-G

80297283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84126759-A-G

80297289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84126753-A-G

80297413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84126658-G-A

80297544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84126527-G-A

80297729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84126336-T-C

80297755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84126311-A-G

80297755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84126311-A-T

80297851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84126232-A-T

http://identifiers.org/hco/15/GRCh38#80297890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84126202-C-A

80298038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84126078-T-C

80298102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84126012-G-A

80298196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84125935-T-G

80303965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84116735-G-A

http://identifiers.org/hco/15/GRCh38#80303979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84116749-C-A

http://identifiers.org/hco/15/GRCh38#80306524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84124482-C-A

80306696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84124633-C-T

80307034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84125013-T-C

80312705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84109299-G-A

80312733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84109275-C-G

80312733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84109275-C-T

80312802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84109205-A-G

80312810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84109197-G-C

80312881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84109124-A-G

80312917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84109088-G-A

80312939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84109066-C-T

80313212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84108839-G-A

80313362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84108070-C-T

http://identifiers.org/hco/15/GRCh38#80313463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84107985-C-A

80313511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84107937-C-T

80313604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84107858-C-T

80313652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84107810-G-A

80313670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84107792-G-A

80313710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84107755-C-G

80314177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84107288-A-G

80314232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84107234-G-A

80314260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84107205-G-A

80314356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84107093-A-G

80314523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84106933-A-G

80314597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84106861-A-T

80314632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84106818-T-C

80314652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84106799-C-T

80314968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84106349-T-C

80315003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84106316-C-T

80315093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84106063-T-C

80315439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84105752-G-A

80315439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84105752-G-C

80315519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84105664-C-T

80315604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84105582-C-G

80315716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84105471-G-A

http://identifiers.org/hco/15/GRCh38#80316001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84105235-C-A

80316080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84105099-A-T

80316223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84104975-C-T

80316252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84104946-T-C

80316255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84104943-A-G

80316298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84104900-A-G

80316778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84104348-C-G

80316826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84104303-G-A

80316885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84104244-A-G

80316948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84104179-G-T

80316987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84104143-C-T

80317031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84104121-T-C

http://identifiers.org/hco/15/GRCh38#80317877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84103200-C-A

80317877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84103200-C-T

http://identifiers.org/hco/15/GRCh38#80317977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84103135-C-A

80317977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84103135-C-T

80318068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84103056-G-A

80318068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84103056-G-C

80318340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84102406-C-G

80318368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84102376-G-T

80319097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84101644-T-C

80319368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84101372-T-G

80319383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84101357-T-C

80319479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84101254-C-T

80319585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84101155-G-A

80319688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84101064-G-T

80319798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84100966-C-T

80319861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84100909-T-G

80320558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84099357-T-C

80320558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84099357-T-G

80320661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84099259-A-T

http://identifiers.org/hco/15/GRCh38#80320855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84098754-A-C

80320964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84098671-A-G

80321019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84098621-G-A

80321019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84098621-G-C

http://identifiers.org/hco/15/GRCh38#80321360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84098307-C-A

80321384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84098292-T-A

80321405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84098272-G-A

80322083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84097894-C-T

80322368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84097607-T-C

80322401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84097574-C-T

80322542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84097434-G-A

80322642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84097333-G-C

80322649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84097326-C-T

80323351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84096627-T-G

80323464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84096506-C-T

80329342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84094297-A-G

http://identifiers.org/hco/15/GRCh38#80329344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84094295-C-A

80329393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84094268-C-G

80329445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84094220-G-A

80329457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84094208-T-C