http://identifiers.org/hco/2/GRCh38#112482203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128907942-C-A

http://identifiers.org/hco/2/GRCh38#112482205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128907944-C-A

112482205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128907944-C-G

112482278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128908014-A-G

http://identifiers.org/hco/2/GRCh38#112482284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128908020-C-A

112482284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128908020-C-T

112482516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128908238-G-A

112482516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128908238-G-T

http://identifiers.org/hco/2/GRCh38#112482630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128908328-C-A

112482630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128908328-C-T

112482766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128908426-C-T

112483229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128908760-G-A

112483229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128908760-G-T

112483235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128908766-G-T

http://identifiers.org/hco/2/GRCh38#112483259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128908790-C-A

112483259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128908790-C-T

http://identifiers.org/hco/2/GRCh38#112483260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128908791-A-C

112483260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128908791-A-G

112483301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128908814-G-A

112483329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128908842-G-T

112483340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128908853-G-C

112483340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128908853-G-T

112483417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128908929-A-G

112483428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128908941-G-A

112483428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128908941-G-C

112483428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128908941-G-T

112483475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128908988-G-T

112483493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128909006-G-T

112483812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128909300-C-T

http://identifiers.org/hco/2/GRCh38#112483895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128909385-C-A

112483895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128909385-C-T

112483981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128909454-T-C

112484001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128909470-C-T

112484060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128909530-A-G

112484688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128909766-A-G

112485053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128910097-G-A

112485053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128910097-G-T

112485358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128910217-C-T

112485700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128910549-A-G

112485700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128910549-A-T

112485813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128910637-G-A

112485831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128910650-G-T

112485845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128910664-G-A

112485845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128910664-G-T

112486204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128911091-G-C

112486364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128911248-A-G

112486645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128911582-C-T

112486953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128911822-G-A

112486953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128911822-G-C

112487085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128911901-T-C

112487188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128912022-A-G

112487386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128912200-A-G

112487637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128912538-C-T

112487655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128912556-T-G

112487760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128912653-G-T

112493935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128917440-T-C

112493963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, undefined
orthologous variants: 128917569-G-A

112493965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, undefined
orthologous variants: 128917571-G-A

112493965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, undefined
orthologous variants: 128917571-G-T

112494032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128917670-T-C

http://identifiers.org/hco/2/GRCh38#112494046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128917684-C-A

112494046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128917684-C-T

112494242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: synonymous variant
orthologous variants: 128917875-A-G

112494418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128918233-G-A

112494421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128918236-A-G

112495013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128918958-A-G

112495033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128918977-G-T

112495034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128918978-G-A

112495072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128919016-C-G

112495249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128919171-C-G

112495249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128919171-C-T

112495257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128919179-A-G

112495386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128919292-A-T

112495450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128919355-G-A

112495527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128919429-A-G

112495545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128919444-G-A

112496033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128919633-C-T

112496214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128919781-A-G

112496325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128919880-T-A

112496354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128919908-G-A

112496384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128919938-G-A

112496464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128920016-C-T

112496465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128920017-A-G

112500716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128922454-A-G

http://identifiers.org/hco/2/GRCh38#112500722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128922460-C-A

112500722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128922460-C-G

112500751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128922488-A-G

112500775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128922509-A-G

112500841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128922591-A-G

112500856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128922606-G-A

112500880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128922635-T-A

112500930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128922723-G-A

112500967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128922787-T-C

112501064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128922961-G-A

112501064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128922961-G-T

http://identifiers.org/hco/2/GRCh38#112501078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128922975-A-C

112501078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128922975-A-G

http://identifiers.org/hco/2/GRCh38#112501085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128922995-A-C

112501085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128922995-A-G

112501085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128922995-A-T

112501173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128923079-G-T

112502772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128923520-T-G

112502808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128923544-T-C

112503187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128924169-T-C

112503187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128924169-T-G

112503240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128924221-A-G

112503240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128924221-A-T

112503252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128924233-G-T

112503253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128924234-A-G

112503280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128924261-A-T

112515469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128925509-A-G

http://identifiers.org/hco/2/GRCh38#112516534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128926707-C-A

112516567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128926739-G-A

112516584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128926756-G-A

112516755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128926878-C-G

112516814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128926929-G-A

http://identifiers.org/hco/2/GRCh38#112516864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128926975-A-C

112516954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128927060-C-T

112519767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128930746-T-C

112520193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128930859-T-A

112520193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128930859-T-G

112520351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128930983-C-T

112520431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128931063-C-G

112520454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128931087-A-G

112520484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128931116-G-C

112520488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128931121-G-A

http://identifiers.org/hco/2/GRCh38#112520589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128931241-C-A

112520594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128931246-T-C

112520609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128931266-T-A

112520609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128931266-T-C

112520609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128931266-T-G

http://identifiers.org/hco/2/GRCh38#112520653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128931312-C-A

112520653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128931312-C-T

112520666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128931324-G-A

112521179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron variant
orthologous variants: 128931647-G-A

112522375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128931923-T-C

http://identifiers.org/hco/2/GRCh38#112522393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128931941-C-A

112522393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128931941-C-T

http://identifiers.org/hco/2/GRCh38#112522421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128931962-A-C

112522421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128931962-A-T

112522466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128932012-T-C

112522490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128932036-G-T

112522604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128932158-A-G

http://identifiers.org/hco/2/GRCh38#112522605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128932159-C-A

112522605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128932159-C-T

112522638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128932191-G-T

http://identifiers.org/hco/2/GRCh38#112522673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128932256-C-A

112522673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128932256-C-T

http://identifiers.org/hco/2/GRCh38#112522876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128932424-C-A

112522904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128932453-C-G

112523035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128932540-C-G

112523049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128932564-G-T

http://identifiers.org/hco/2/GRCh38#112528764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128934944-A-C

112528774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128934954-A-G

112528774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128934954-A-T

112528780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128934960-C-T

112528784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128934964-A-T

112528972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128935135-G-A

112528972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128935135-G-C

112528972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128935135-G-T

112529077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128935295-G-A

112529077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128935295-G-T

http://identifiers.org/hco/2/GRCh38#112529124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128935340-A-C

112529124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128935340-A-G

112529148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128935363-C-G

112529200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128935408-G-T

http://identifiers.org/hco/2/GRCh38#112529337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128935521-C-A

112529337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128935521-C-T

112529623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128935813-C-T

112529706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128935895-C-T

112529734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128935915-T-C

http://identifiers.org/hco/2/GRCh38#112529749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128935928-C-A

112529749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128935928-C-T

http://identifiers.org/hco/2/GRCh38#112529754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128935933-A-C

112529777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128935955-G-T

112529879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128936055-G-T

http://identifiers.org/hco/2/GRCh38#112529894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128936072-C-A

112529894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128936072-C-T

112529905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128936083-G-A

112530018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128936192-A-G

112530018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128936192-A-T

112530037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128936210-T-C

112530044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128936217-A-G

http://identifiers.org/hco/2/GRCh38#112530082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128936255-C-A

112530082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128936255-C-G

http://identifiers.org/hco/2/GRCh38#112530102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128936275-C-A

http://identifiers.org/hco/2/GRCh38#112530255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128936420-C-A

112530369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128936514-A-T

112530487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128936629-C-T

112531226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128937033-T-C

112531333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128937135-T-C

112531363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128937165-G-A

112531376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128937177-T-C

http://identifiers.org/hco/2/GRCh38#112531420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128937215-C-A

112531566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128937353-A-G

http://identifiers.org/hco/2/GRCh38#112531567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128937354-C-A

112531567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128937354-C-T

112531585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128937372-A-G

112531615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128937402-G-A

112531615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128937402-G-T

112531770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128937547-G-C

112531784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128937561-G-T

112531803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128937580-A-G

112532016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128937796-T-C

http://identifiers.org/hco/2/GRCh38#112532185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128937974-C-A

http://identifiers.org/hco/2/GRCh38#112532295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128938092-C-A

112532295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128938092-C-G

http://identifiers.org/hco/2/GRCh38#112532450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21586
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128938242-C-A