64561478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92793349-T-C

64561478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92793349-T-G

64561509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92793380-C-G

64561509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92793380-C-T

64561635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 92793508-G-A

64561728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 92793601-G-A

64561728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 92793601-G-C

http://identifiers.org/hco/3/GRCh38#64561783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92793656-C-A

64561783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92793656-C-G

64561783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92793656-C-T

http://identifiers.org/hco/3/GRCh38#64561858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92793723-C-A

64561858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92793723-C-G

64561858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92793723-C-T

64562079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92793927-G-T

http://identifiers.org/hco/3/GRCh38#64562402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92794245-C-A

64562517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92794348-C-T

64562616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92794450-T-C

64562832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92794661-A-G

http://identifiers.org/hco/3/GRCh38#64562859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92794689-C-A

64562987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92794783-T-C

64563013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92794803-A-G

64563062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92794852-G-A

64563062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92794852-G-C

64563062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92794852-G-T

64563411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92795167-T-C

64563448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92795209-T-C

64563459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92795220-T-C

64563554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92795619-T-C

64563722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92795789-C-T

64564021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92796081-C-T

64564024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92796084-G-A

http://identifiers.org/hco/3/GRCh38#64564108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92796122-C-A

64564187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92796193-G-C

64564187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92796193-G-T

http://identifiers.org/hco/3/GRCh38#64564289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92796291-A-C

64564400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92796406-T-A

64564400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92796406-T-C

64565252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92797234-G-C

64565252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92797234-G-T

64565282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92797265-T-C

64565360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92797338-A-G

64565375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92797353-G-A

64565457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92797422-G-T

http://identifiers.org/hco/3/GRCh38#64565465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92797430-C-A

64565486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92797455-G-A

64565486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92797455-G-T

64565596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92797561-C-T

64565654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92797622-T-G

64565808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92797769-T-C

64566001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92797980-T-G

64566027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798006-C-T

http://identifiers.org/hco/3/GRCh38#64566154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92798130-C-A

64566356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798291-T-A

64566470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798328-G-A

http://identifiers.org/hco/3/GRCh38#64566529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92798382-C-A

64566689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798555-T-C

64566852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798720-G-A

64566852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798720-G-T

64566961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798827-G-A

64566996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798851-T-C

64567615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92799343-G-A

64567615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92799343-G-C

64567705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92799382-C-T

64567785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92799475-C-T

64567786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92799476-G-A

64567786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92799476-G-T

64568070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92800078-A-T

http://identifiers.org/hco/3/GRCh38#64568305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92800267-C-A

64568305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92800267-C-T

64568307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92800269-C-G

64568307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92800269-C-T

http://identifiers.org/hco/3/GRCh38#64568320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92800283-C-A

64568320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92800283-C-G

64568320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92800283-C-T

http://identifiers.org/hco/3/GRCh38#64568326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92800289-C-A

64568577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92800543-T-A

64568577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92800543-T-C

64568577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92800543-T-G

64568636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92800622-G-C

64568761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92800758-G-A

64568761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92800758-G-T

http://identifiers.org/hco/3/GRCh38#64568764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92800761-C-A

64568764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92800761-C-T

64568765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92800762-A-G

http://identifiers.org/hco/3/GRCh38#64568768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92800765-C-A

64568768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92800765-C-G

64568852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92800849-G-C

http://identifiers.org/hco/3/GRCh38#64568937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92800928-C-A

64568960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92800951-T-A

64568960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92800951-T-C

64568960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92800951-T-G

64569007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92800998-C-T

64569296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92801295-G-A

64569400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92801397-C-T

64569931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92801911-T-C

64570438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92802415-G-T

64570516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92802491-G-A

64570906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92803248-G-A

64570906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92803248-G-T

64570907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92803249-A-G

64570967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92803308-A-T

64571364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92803715-A-G

64571364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92803715-A-T

64571564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92803909-T-G

64571815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92804163-C-T

64572117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92804482-G-A

64572180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92804560-T-C

64572402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92804780-G-A

http://identifiers.org/hco/3/GRCh38#64572421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92804803-C-A

64572649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92805019-G-A

64572685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92805055-A-G

http://identifiers.org/hco/3/GRCh38#64572689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92805059-A-C

64572774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92805159-C-T

64573269-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92805269-T-A

64573425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92805415-A-G

64573506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92805493-G-A

64573765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92805725-T-C

64573927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92805862-T-C

64573973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92805906-A-T

64574066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92805994-C-T

64574130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92806040-G-A

64574337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92806251-G-A

http://identifiers.org/hco/3/GRCh38#64574471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92806309-C-A

64574471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92806309-C-T

64574482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92806320-G-A

64574766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92806366-T-A

64574816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92806409-C-T

64574910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92806505-C-T

http://identifiers.org/hco/3/GRCh38#64574929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92806524-A-C

64574932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92806527-T-C

64574938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92806533-G-T

64574973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92806566-A-G

64575395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92806957-C-T

64575433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92806993-T-C

64576072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92807794-G-C

64576077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92807799-A-G

http://identifiers.org/hco/3/GRCh38#64576352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92808069-C-A

http://identifiers.org/hco/3/GRCh38#64576666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92808281-A-C

64576691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92808306-C-T

64576792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92808413-A-G

64576834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92808455-G-A

64576834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92808455-G-C

http://identifiers.org/hco/3/GRCh38#64576948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92808499-C-A

64576948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92808499-C-T

64576972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92808523-C-T

64577309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92808832-C-T

64577471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92808971-T-C

64577548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92810231-G-C

64577807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92810477-A-G

64577813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92810483-G-A

64577903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92810564-C-T

64578006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92810999-T-C

64578006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92810999-T-G

64578273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92811240-C-T

64578314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92811278-A-G

64578446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92811410-C-G

64578446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92811410-C-T

64578655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92811574-A-G

64578681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92811600-T-C

64578690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92811609-A-T

64578728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92811647-T-C

64578909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92811828-T-C

64579095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92811989-C-T

http://identifiers.org/hco/3/GRCh38#64579219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92812107-A-C

64579219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92812107-A-G

64579496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92812333-C-T

64579618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92812519-C-T

64579833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92812715-C-T

http://identifiers.org/hco/3/GRCh38#64579865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92812746-C-A

64579934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92812815-A-T

64579967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92812848-C-T

64579990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92812872-C-G

64579990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92812872-C-T

64580203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92813495-G-T

64580231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92813522-G-A

64580247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92813537-G-T

64580349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92813623-T-G

64580358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92813632-T-C

http://identifiers.org/hco/3/GRCh38#64580410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92813682-C-A

64580482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92813754-T-C

64580499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92813771-C-T

64580706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92813957-A-T

64580755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92814001-A-G

64580790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92814036-C-G

http://identifiers.org/hco/3/GRCh38#64580991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92814208-A-C

64581127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92814345-C-T

64581132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92814350-C-G

64581132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92814350-C-T

64581197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92814416-T-C

64581426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

64581434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

64581692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92814891-G-T

64581880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92815062-A-G

64581902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92815083-C-G

64581941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92815120-A-G

64582041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92815715-T-C

64582230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92815910-A-G

64582403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92816074-T-C

64582481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92816159-G-C

64582482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92816160-G-A

64582499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92816176-A-G

64582513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92816190-C-T

64582542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92816219-G-A

http://identifiers.org/hco/3/GRCh38#64582652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92816325-C-A

64582654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92816327-A-G

http://identifiers.org/hco/3/GRCh38#64582662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92816335-C-A

http://identifiers.org/hco/3/GRCh38#64582677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92816350-C-A

64582695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92816369-T-C

http://identifiers.org/hco/3/GRCh38#64582830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92816509-A-C

http://identifiers.org/hco/3/GRCh38#64582959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92816644-C-A

64583234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92816872-C-T

64583260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92816897-T-C

64583316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92816959-C-T

64583405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92817054-A-G

http://identifiers.org/hco/3/GRCh38#64583407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92817056-A-C

64583407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92817056-A-T

http://identifiers.org/hco/3/GRCh38#64583603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92817195-C-A

64583648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92817252-A-G

64583684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92817289-G-A

64583684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92817289-G-T

64583718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92817323-C-T

64583837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92817436-A-G

http://identifiers.org/hco/3/GRCh38#64583865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92817463-C-A

64583865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92817463-C-T

64584061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92817645-A-G

64584150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92817737-C-T

64584351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92817926-T-C

64584577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92818128-T-C

64584665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92818202-T-C

64584665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92818202-T-G

64584666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92818203-A-G

64584718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92818244-C-T

64586639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92818589-T-C

http://identifiers.org/hco/3/GRCh38#64586781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92818813-C-A

64586890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92818922-T-C

64587043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92819074-C-T

64587057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92819088-G-A

64587080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92819110-G-A

64587549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92819840-G-A

64587624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92819912-T-C

64588232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92820574-G-A

64588469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92820814-C-T

64588488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92820823-A-G

64588500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92820835-T-C

http://identifiers.org/hco/3/GRCh38#64588572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92820910-C-A

http://identifiers.org/hco/3/GRCh38#64588710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92821019-C-A

http://identifiers.org/hco/3/GRCh38#64588816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92821138-C-A

64588819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92821141-G-C

64588819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92821141-G-T

64588908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92821231-A-G

64589146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92821515-G-A

64589239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92821615-T-C

64589271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92821647-G-A

64589271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92821647-G-T

64589440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92821798-G-T

64589465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92821825-G-T

64589482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92821839-C-T

64589630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92821954-T-C

64589686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92822010-T-C

64589728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92822041-G-A

64589728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92822041-G-T

64590031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92822300-T-G

64590467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92822758-T-C

64590474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92822765-T-C

64590839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92823115-A-G

64590968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92823237-T-C

64590994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92823263-C-T

64591082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92823351-A-G

64591713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92823790-G-A

64591718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92823795-A-G

64591941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92824030-C-T

64592326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92824415-A-G

64592700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92824834-G-C

64592754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92824888-C-T