52164329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 101240022-A-G

52164331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 101240026-G-A

52164331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 101240026-G-T

52165061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101241001-G-A

52165061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101241001-G-T

52165076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101241016-T-C

52165098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101241030-C-T

52165270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101241158-G-A

52165305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101241192-A-G

52165372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101241265-G-A

52165429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101241301-C-T

52165585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101241404-C-T

52165604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101241427-T-C

52165903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101241725-G-T

52165961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101241783-C-T

http://identifiers.org/hco/12/GRCh38#52167534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101243352-A-C

52167917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101243709-C-T

52167944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101243736-C-G

52167944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101243736-C-T

52168390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101245684-G-A

52168693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101245898-G-C

52168735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101245951-A-G

52168736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101245952-C-T

52168785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101246012-G-A

52168897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101246105-G-A

52168897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101246105-G-T

52169651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246303-G-T

http://identifiers.org/hco/12/GRCh38#52169708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#101246360-A-C

52169932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246571-T-A

52169932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246571-T-C

52169994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246634-G-T

52170001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246641-G-A

52170001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246641-G-T

52170019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246662-G-A

52170019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246662-G-C

52170019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246662-G-T

52170180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246801-G-A

52170180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246801-G-T

52170266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246886-G-T

52170295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246915-T-G

52170343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246928-G-A

52170343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246928-G-C

52170343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246928-G-T

52170375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246934-A-G

52170375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246934-A-T

http://identifiers.org/hco/12/GRCh38#52170411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#101246959-C-A

52170411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246959-C-T

52170436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246984-G-A

52170436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101246984-G-T

http://identifiers.org/hco/12/GRCh38#52170533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#101247066-C-A

http://identifiers.org/hco/12/GRCh38#52170632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#101247155-C-A

52170632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101247155-C-T

52170652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101247174-G-A

52170839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101247289-G-A

52170839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101247289-G-T

52170855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101247305-A-G

http://identifiers.org/hco/12/GRCh38#52170887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#101247332-C-A

52170887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101247332-C-T

52170935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101247376-C-T

52170965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101247409-G-A

52171021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101247466-A-G

52171021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101247466-A-T

http://identifiers.org/hco/12/GRCh38#52171070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#101247510-C-A

52171070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101247510-C-T

52171077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101247517-A-G

52171124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101247556-T-C

52171219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101247635-G-A

52171219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101247635-G-T

52171278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101247689-A-G

52171278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101247689-A-T

http://identifiers.org/hco/12/GRCh38#52171305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#101247706-C-A

52171404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101247802-T-C

52171557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 101247953-G-A

52171587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101247982-G-C

52171617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101248010-A-T

http://identifiers.org/hco/12/GRCh38#52171704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#101248096-C-A

52171704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101248096-C-T

52171837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101248241-G-A

52171837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101248241-G-T

http://identifiers.org/hco/12/GRCh38#52172165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#101248855-C-A

52172165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101248855-C-T

52172343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101249022-G-A

52172343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101249022-G-T

52172362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101249041-G-A

52172469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249132-G-A

52172469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249132-G-T

52172489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249151-G-A

52172489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249151-G-C

52172489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249151-G-T

52172565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249199-C-T

52172730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249287-C-T

52172777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249329-C-G

52172787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249340-G-C

http://identifiers.org/hco/12/GRCh38#52172898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249423-C-A

52172927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249449-T-C

52172943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249465-G-A

52172943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249465-G-T

http://identifiers.org/hco/12/GRCh38#52172946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249468-C-A

52172946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249468-C-T

52172969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249490-T-C

52172980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249501-T-C

52172985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249504-G-A

52172985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249504-G-C

52172985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249504-G-T

52172994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249513-C-T

52172996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249515-T-C

52173050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101249567-A-G

52173050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101249567-A-T

http://identifiers.org/hco/12/GRCh38#52173068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249585-C-A

52173071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101249588-C-T

52173137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101249654-G-A

52173137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101249654-G-C

52173140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101249657-C-T

52173190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249709-G-A

52173190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249709-G-T

http://identifiers.org/hco/12/GRCh38#52173211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249743-C-A

52173211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249743-C-G

52173211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249743-C-T

http://identifiers.org/hco/12/GRCh38#52173225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249756-C-A

52173225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249756-C-T

http://identifiers.org/hco/12/GRCh38#52173255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249784-C-A

http://identifiers.org/hco/12/GRCh38#52173277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249829-C-A

52173277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249829-C-G

52173277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249829-C-T

http://identifiers.org/hco/12/GRCh38#52173278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249830-C-A

52173278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249830-C-T

http://identifiers.org/hco/12/GRCh38#52173283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249835-C-A

52173283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249835-C-G

52173331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249880-C-T

52173332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249881-T-C

52173415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249935-T-C

http://identifiers.org/hco/12/GRCh38#52173474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249975-C-A

52173474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249975-C-T

52173476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249977-T-A

52173476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249977-T-G

http://identifiers.org/hco/12/GRCh38#52173481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249980-C-A

52173481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249980-C-G

52173481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249980-C-T

http://identifiers.org/hco/12/GRCh38#52173520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101250017-C-A

52173520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101250017-C-G

52173520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101250017-C-T

52173543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101250040-C-T

52173668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101250126-C-T

52173746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101250204-C-T

52173787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101250246-G-A

52173787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101250246-G-T

52174012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101250406-A-G

52174580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101250789-C-T

52174581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101250790-G-A

52174592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101250794-T-C

52175001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101251168-G-A

52175176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101251345-G-A

52175439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101251544-G-A

52175465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101251567-C-T

52175949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101252006-T-G

52176013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101252066-A-T

52176209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101252273-C-T

52176210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101252274-G-A

52176287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101252335-G-T

52176354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101252417-G-A

52178794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101255202-C-T

http://identifiers.org/hco/12/GRCh38#52178886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101255301-C-A

52178905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101255317-G-A

52179383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101255630-G-C

http://identifiers.org/hco/12/GRCh38#52179600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101255789-C-A

52179613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101255794-C-G

52179996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101256179-C-T

52180037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101256222-C-G

52180037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101256222-C-T

52180385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101256477-G-A

52180385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101256477-G-T

52180422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101256505-G-C

52180422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101256505-G-T

52180654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101256669-T-C

52180693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101256698-G-A

52180789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101256783-G-A

52180849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101257305-A-G

52180861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101257326-G-A

52180861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101257326-G-C

52180861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101257326-G-T

52180892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101257352-G-A

52181008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101257461-T-A

52181008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101257461-T-C

52181060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101257508-T-A

52181243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101257743-C-G

52181878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101258385-T-C

52181985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101258481-C-T

52182251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101258707-T-A

52183004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101260099-G-A

52183064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101260154-A-G

52183069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101260159-A-G

http://identifiers.org/hco/12/GRCh38#52183397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101260472-C-A

52183397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101260472-C-T

52184015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101260849-G-T

52184190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101261013-G-A

52184190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101261013-G-T

52184604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101261371-C-T

52184640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101261401-A-G

52184871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101261638-T-C

52184965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101261715-C-T

52185051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101261808-T-C

52185163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101261904-G-T

52185252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101261966-A-G

52185280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101261994-A-G

52185380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 101262092-T-C

52185459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101262171-C-T

52185531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101262243-C-T

52185534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101262246-C-T

http://identifiers.org/hco/12/GRCh38#52185647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#101262352-C-A

52185647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101262352-C-G

52185647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101262352-C-T

52185653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101262358-G-C

52185740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101262452-T-C

52185814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101262521-A-G

52186049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101262729-C-T

52186183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101263643-C-G

52187772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101264160-G-C

52187772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101264160-G-T

52187827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101264214-C-G

52187827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101264214-C-T

52187887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101264274-G-A

52188262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101264604-G-A

52188605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101264974-A-G

52188934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101265271-C-T

52188972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101265288-C-T

52189115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101265431-G-C

52189117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101265433-T-G

52190017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101266190-C-T

52190150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101266262-G-A

52190506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101266682-G-A

52190626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101266754-T-C

52190676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101266797-A-G

52191111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101267171-G-A

52191113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101267173-A-G

52191123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101267183-C-T

52191249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101267325-G-A

52191249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101267325-G-T

52191278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101267351-C-T

http://identifiers.org/hco/12/GRCh38#52191566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101267597-C-A

52191566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101267597-C-T

52191903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101267936-G-A

52191903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101267936-G-T

http://identifiers.org/hco/12/GRCh38#52191971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#101268006-C-A

52191971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101268006-C-G

52191971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101268006-C-T

52192181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101268209-C-T

52192225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101268245-A-G

52192225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101268245-A-T

52192229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101268249-T-G

52192242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101268262-T-G

52192253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101268278-T-G

52192302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101268333-G-C

52192428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101268455-G-A

52192428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101268455-G-T

52192572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101268569-A-G

52192588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101268585-C-T

52192615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101268611-C-T

52192738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101268742-T-C

52192946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101268927-C-T

52192954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101268937-A-T

52192957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101268940-T-C

http://identifiers.org/hco/12/GRCh38#52192965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101268948-A-C

52193015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101268971-C-T

52193141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101269071-T-C

52193242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101269132-G-A

52193424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101269284-C-G

52193732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101269556-A-G

52194287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101269945-C-T

52194345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101269994-C-T

52194357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101270006-C-G

52196722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101271030-A-T

52196834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101271137-G-A

52196835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101271138-A-G

52197206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101271411-C-G

52197206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101271411-C-T

52197207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101271412-T-G

52197522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101271698-C-T

52197549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101271723-A-T

52197562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101271736-C-G

52197616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101271789-T-C

52197761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101271906-G-C

52197808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101271949-G-A

52198021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101272154-G-A

52198722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101273013-G-C

52198853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101273132-G-A

52198884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101273167-G-A

52199051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101273341-G-A

52199223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101273413-G-C

52199266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101273450-T-C

52199276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101273459-G-A

52199370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101273561-C-T

http://identifiers.org/hco/12/GRCh38#52199414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101273611-C-A

52199414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101273611-C-T

52199519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101273726-C-T

52199875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101274111-A-G

52199964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101274189-C-T

52199965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101274190-G-A

52200172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101274397-A-G

52200346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101274537-G-A

52200346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101274537-G-C

52200540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101274634-A-G

52200721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101274787-C-T

52200779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101274844-T-C

52202762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101275941-G-A

52202791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101275965-T-C

52202837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101276024-A-G

52203130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101276354-C-G

http://identifiers.org/hco/12/GRCh38#52203226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101276488-C-A

52203245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101276513-G-A

52203347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101276620-G-A

52203382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101276651-G-T

52203618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101276882-G-A

52204073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277335-C-T

52204187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277442-A-G

52204554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277649-T-A

52204557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277652-G-A

52204557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277652-G-C

52204557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277652-G-T

52204642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101277735-A-G

52204841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101277941-T-C

52205290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101278173-C-T

52205345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101278229-G-A

52205623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101279024-T-A

52205623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101279024-T-G

http://identifiers.org/hco/12/GRCh38#52205645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101279046-C-A

http://identifiers.org/hco/12/GRCh38#52205665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101279066-C-A

52205665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101279066-C-T

52205666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101279067-A-G

52205730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101279156-G-T

52205766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101279190-T-A

http://identifiers.org/hco/12/GRCh38#52205804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101279228-C-A

52205804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101279228-C-G

52205815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101279239-A-G

52205895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101279317-T-C

52205903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101279325-T-G

52205924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101279346-T-C

http://identifiers.org/hco/12/GRCh38#52206034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101279452-A-C

52206034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101279452-A-G

52206203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101279594-G-A

http://identifiers.org/hco/12/GRCh38#52206239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101279631-C-A

52206239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101279631-C-T

52206270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101279653-T-A

52206270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101279653-T-C

52206310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101279703-G-C

52206310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101279703-G-T

52206325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101279718-G-A

52206325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101279718-G-T

52206344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101279737-G-A

52206390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101279767-G-A

http://identifiers.org/hco/12/GRCh38#52206410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101279787-C-A

http://identifiers.org/hco/12/GRCh38#52206411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101279788-A-C

http://identifiers.org/hco/12/GRCh38#52206414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101279791-A-C

52206414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101279791-A-G

52206423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101279800-T-A

52206423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101279800-T-C

http://identifiers.org/hco/12/GRCh38#52206442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101279819-A-C

52206442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101279819-A-G

52206458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101279837-C-G

52206469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101279848-G-T

http://identifiers.org/hco/12/GRCh38#52206513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101279892-C-A

52206513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 101279892-C-T

52206549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101279915-T-C

52206621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101279977-C-G

52206621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101279977-C-T

52206648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 101280000-G-A

52206648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 101280000-G-T

52206683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101280033-T-C

http://identifiers.org/hco/12/GRCh38#52206700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101280050-C-A

52207674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101280463-G-A

52207773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101280562-T-C

52207859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101280637-C-T

52207889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101280666-A-G

52207927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101280700-C-T

52207957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101280729-G-C

52207957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101280729-G-T

http://identifiers.org/hco/12/GRCh38#52207973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101280745-C-A

52207973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101280745-C-T

52208020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101280812-G-T

52208121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101280916-T-G

52208244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101281038-G-A

http://identifiers.org/hco/12/GRCh38#52208334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101281105-C-A

52208699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101281248-A-T

52208712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101281261-T-A

52208712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101281261-T-G

52208788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101281338-C-T

52208933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101281441-G-A

52209219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101281675-T-C

http://identifiers.org/hco/12/GRCh38#52209256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101281711-A-C

52209256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101281711-A-G

52209309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101281761-T-A

52209500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101281984-G-A

52209514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101281998-C-T

52209561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101282041-C-T

52209597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101282077-T-C

http://identifiers.org/hco/12/GRCh38#52209723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101282186-C-A

52209723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101282186-C-T

52209784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101282241-G-A

52209784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101282241-G-T

52209802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101282255-T-A

52209937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101282386-G-C

52209937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101282386-G-T

52210087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101282500-G-A

http://identifiers.org/hco/12/GRCh38#52210119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101282532-C-A

52210119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101282532-C-T

52210120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101282533-G-A

52210120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101282533-G-C

52210170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101282583-G-A

52210194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101282607-C-T

52210457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101282822-C-T

52210632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101282936-G-A

52210632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101282936-G-T

52210911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101283149-A-G

52211049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101283261-T-C

52211071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101283295-G-A

52211071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101283295-G-T

http://identifiers.org/hco/12/GRCh38#52211073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101283297-C-A

52211122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101283329-G-A

52211122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101283329-G-C

52211122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101283329-G-T

52211151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101283359-G-T

52211156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101283364-G-A

52211158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101283366-G-A

52211261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101283464-T-C

52211370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101283575-A-G

52211490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101283705-G-A

52211978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101284037-T-C

52211978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101284037-T-G

52212007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101284044-G-A

52212007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101284044-G-C

52212007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101284044-G-T

52212008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101284045-G-A

52212008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101284045-G-T

52212012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101284049-C-T

52212365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101284185-T-C

http://identifiers.org/hco/12/GRCh38#52212624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101284344-C-A

52212624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101284344-C-T

52212725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 101284440-G-A

52212725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 101284440-G-T

52212917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101284601-G-A

52212917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101284601-G-C

52212917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101284601-G-T

http://identifiers.org/hco/12/GRCh38#52212951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101284646-C-A

52212951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101284646-C-T

52212963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101284658-G-A

52212963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101284658-G-T

52213137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101284847-G-A

52213137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101284847-G-C

52213137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101284847-G-T

http://identifiers.org/hco/12/GRCh38#52213252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101284964-C-A

52213252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101284964-C-T

http://identifiers.org/hco/12/GRCh38#52213325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101285007-C-A

52213338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101285020-C-T

http://identifiers.org/hco/12/GRCh38#52213442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#101285097-C-A

52213442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101285097-C-T

52213445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101285100-C-T

52213738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101285392-G-A

52214112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101285503-C-T

52214144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101285532-G-A

52214171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101285558-T-C

52214179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101285563-C-T

52214248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101285622-G-A

52215919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101286462-G-T

52215982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101286525-G-T

http://identifiers.org/hco/12/GRCh38#52216032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101286550-C-A

52216032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101286550-C-T

52216035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101286553-C-T

52216161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101286670-C-T

52216641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101287449-A-T

52216684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101287490-A-G

52217224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101288030-C-G

52217224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101288030-C-T

52218448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101289493-A-G

52220622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101291343-T-G

52220667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101291381-G-C

52220809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101291494-A-G

http://identifiers.org/hco/12/GRCh38#52221474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101292025-C-A

52221602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101292156-A-G

52221998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101292555-G-T

http://identifiers.org/hco/12/GRCh38#52222061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#101292624-C-A

52222061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101292624-C-T

52222157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101292826-G-A

http://identifiers.org/hco/12/GRCh38#52222167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#101292836-C-A

52222172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101292841-G-A

52222172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101292841-G-T

52222218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101292929-T-C

52222285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101292993-G-A