http://identifiers.org/hco/3/GRCh38#2110439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#105664804-C-A

2110524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105664889-G-A

http://identifiers.org/hco/3/GRCh38#2110556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#105664920-C-A

2110573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105664937-T-C

http://identifiers.org/hco/3/GRCh38#2110579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#105664942-C-A

2110590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105664953-G-C

2110652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105665014-A-G

2110740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105665071-G-C

2110740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105665071-G-T

2110743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105665074-G-T

2110753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105665084-G-T

2110804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105665135-C-G

2110804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105665135-C-T

2110906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105665409-T-G

2111341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105665865-A-G

2111353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105665878-A-T

http://identifiers.org/hco/3/GRCh38#2111486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#105665986-C-A

2111486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105665986-C-G

2111616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105666112-G-T

2111637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105666133-A-G

2111645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105666141-T-C

2111964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105667131-A-G

2112040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105667211-G-T

2112113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105667280-T-C

2112137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105667304-A-G

2112399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105667575-T-G

2112446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105667622-G-A

2112446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105667622-G-T

2112750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105667922-G-C

2112762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105667934-G-A

2112788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105667958-T-A

2112788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105667958-T-G

2112830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105667998-G-A

2112880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105668050-T-C

2112976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105668144-A-G

2113041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105668844-A-G

2113140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105668943-T-C

2113178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105668981-G-A

2113234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105669013-A-T

2113355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105669115-G-A

2113490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105669234-A-G

2113490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105669234-A-T

2113526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105669277-G-C

2113746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105669619-G-A

2114003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105669899-C-T

2114026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105669922-T-G

2114842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105670875-G-A

2115109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105671369-G-C

2115363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105671779-C-T

2115465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105671857-T-G

2115567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105671964-C-T

2115705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105672107-A-G

2115770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105672173-G-A

2116359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105672626-G-A

2116509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105672774-A-G

2116526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105672792-G-A

http://identifiers.org/hco/3/GRCh38#2116544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#105672810-A-C

2116544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105672810-A-T

2116838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105673065-A-T

http://identifiers.org/hco/3/GRCh38#2118148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#105674884-A-C

2118561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105677739-G-A

2118807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105677953-C-T

2118937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105678082-T-G

2119092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105678223-G-A

2119100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105678231-T-C

2119159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105678291-G-A

2119172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105678304-G-A

2119369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105678586-A-G

2119383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105678662-C-T

2119472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105678777-A-T

2119906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105679181-A-G

2120123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105679379-A-G

http://identifiers.org/hco/3/GRCh38#2120316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#105679794-C-A

2120316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105679794-C-G

2121524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105680187-G-A

2121524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105680187-G-T

http://identifiers.org/hco/3/GRCh38#2121631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#105680277-C-A

http://identifiers.org/hco/3/GRCh38#2121660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#105680304-A-C

2121660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105680304-A-G

2121660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105680304-A-T

2122264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105680584-C-G

http://identifiers.org/hco/3/GRCh38#2122417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#105680846-A-C

2122502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105680935-G-T

http://identifiers.org/hco/3/GRCh38#2122821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#105682122-C-A

2122826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105682127-A-T

http://identifiers.org/hco/3/GRCh38#2122856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#105682157-A-C

2122863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105682164-A-G

2123160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105682416-A-T

2123331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105682601-C-G

2123377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105682667-T-C

2123497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105682786-G-A

2123508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105682797-C-G

2123582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105682860-T-C

2123729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105683001-T-C

2123938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105683217-G-A

http://identifiers.org/hco/3/GRCh38#2124016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#105683272-C-A

2125987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105684538-C-T

2125993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105684544-G-T

2126098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105684633-T-C

2126124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105684659-C-T

2126284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105685223-A-G

2126438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105685365-C-T

2126651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105685583-T-C

2126875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105685806-G-C

2126933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105685864-G-C

http://identifiers.org/hco/3/GRCh38#2126994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#105685939-C-A

2127128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105686034-A-G

2127128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105686034-A-T

2127203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105686097-C-T

2127291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105686171-G-A

2127291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105686171-G-C

2127291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105686171-G-T

2127478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105686343-C-T

2127512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105686384-C-G

2127512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105686384-C-T

2127680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105686553-T-A

2127710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105686583-C-T

2128033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105686902-G-A

2128053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105686922-C-T

2128452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105687324-G-T

2128509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105687370-G-A

2128681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105687520-G-A

2128684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105687523-T-A

2128770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105687607-T-C

2128832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105687663-A-T

2129476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105688288-T-C

2129504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105688317-C-T

2129547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105688360-C-G

2129547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105688360-C-T

2129845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105689435-C-T

2131364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105690839-C-T

2131436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105690903-C-G

2131528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105691016-G-A

2131560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105691048-C-T

2131857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105691370-G-C

2132141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105691630-A-G

2132303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105691780-C-T

2132308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105691785-A-G

2132591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105692060-A-G

2132591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105692060-A-T

2132907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105692376-C-T

2132921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105692390-G-A

2133052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105692521-A-G

2133145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105692621-T-G

2133240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105692711-C-T

2133262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105692733-A-G

http://identifiers.org/hco/3/GRCh38#2133298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#105692767-C-A

2133751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105693177-T-C

2133751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105693177-T-G

2133764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105693200-C-G

2133764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105693200-C-T

2133905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105693232-A-G

2134165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105693323-T-C

2134171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105693328-C-G

2134202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105693359-T-A

2134268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105693415-C-T

2134273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105693420-A-G

2134355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105693500-G-A

2134425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105693589-T-A

2134463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105693635-A-G

2134517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105693689-T-C

2134518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105693690-C-T

2134747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105693908-A-G

2134983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105694160-G-A

http://identifiers.org/hco/3/GRCh38#2135115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#105694283-A-C

2135258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105694397-G-A

2135300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105694439-G-C

2135350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105694486-T-C

2136700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105698870-A-G

2136756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105698926-C-T

2137366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105699479-C-T

2137441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105699535-T-G

2137454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105699548-G-A

2137567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105699661-A-G

2137593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105699687-T-G

2137648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105699742-G-T

2137652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105699746-T-C

2138039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105700013-T-G

2138079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105700029-T-G

2138702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105700460-A-G

2138923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105700721-G-A

2138938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105700733-A-G

2139477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105701250-G-A

2139567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105701339-G-A

2139620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105701392-A-G

2139673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105701445-G-A

2139673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105701445-G-T

2139738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105701510-C-T

http://identifiers.org/hco/3/GRCh38#2141258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#105706730-A-C

2141342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105706796-G-A

2141445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105706933-C-G

2141445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105706933-C-T

http://identifiers.org/hco/3/GRCh38#2141502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#105706989-C-A

2141502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105706989-C-T

2141548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105707036-T-G

2142097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105707532-G-A

2142680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39986
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105707904-C-T