114006138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43763685-T-C

114006160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43763656-G-T

114006161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43763655-G-C

114006177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43763637-G-A

114006857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43762930-C-T

114007220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43762650-T-A

114007306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43762574-C-T

114007579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43762305-G-C

114008544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43761456-A-G

114009644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43761170-T-C

114009944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43760869-G-A

114010197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43760394-T-A

114010516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43759789-C-T

114010629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43759676-A-G

114010629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43759676-A-T

114010673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43759626-T-C

114010689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43759611-G-A

114010689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43759611-G-T

114010705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43759595-T-G

114010732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43759577-C-T

114010817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 43759479-A-G

114010817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 43759479-A-T

114010911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43759385-G-C

114011035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43759261-C-G

114011152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43759157-T-A

114011698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43758645-C-T

114012389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43757010-G-A

114012403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43756996-T-C

114013872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43755895-C-T

114013993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43755764-T-C

114015703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43754808-A-G

114016856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43753130-C-T

http://identifiers.org/hco/3/GRCh38#114017123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43752922-A-C

114017123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43752922-A-G

114017123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43752922-A-T

114017216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43752829-C-T

114017398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43752725-G-A

114017430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43752693-T-C

114018624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43751803-G-T

114018725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 43751698-C-T

114018881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43751542-T-C

114019102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43751300-T-A

114020186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43750363-C-T

http://identifiers.org/hco/3/GRCh38#114020628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43749389-A-C

114020690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43749092-T-G

114020937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43748376-A-G

http://identifiers.org/hco/3/GRCh38#114021158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43748175-A-C

114021203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43748133-T-A

114021396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43747946-T-C

114021405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43747937-T-A

114021872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43746123-T-C

http://identifiers.org/hco/3/GRCh38#114024965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43744627-A-C

114025249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43744402-T-C

114025315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43744365-G-A

114025315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43744365-G-T

114025589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43744109-G-A

114025630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43744066-G-T

http://identifiers.org/hco/3/GRCh38#114025721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43743999-C-A

114025721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43743999-C-T

114025946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43743803-C-T

114026372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43743428-C-T

114026519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43743309-C-G

114026829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43742986-A-T

http://identifiers.org/hco/3/GRCh38#114026893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43742921-C-A

114027087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43742735-C-T

114027132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43742691-G-A

114027559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43742354-G-A

114027894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43742150-G-A

114027980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43742083-G-A

114028018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43742045-G-A

114028140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43741935-A-T

114028424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43741834-T-C

114029138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43741320-G-C

114029138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43741320-G-T

114029331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43741146-T-C

114029335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43741142-T-C

114030264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43739996-A-T

114030412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43739848-C-T

http://identifiers.org/hco/3/GRCh38#114030475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43739119-A-C

114030718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43738911-C-T

114030777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43738848-T-C

114031079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43736728-A-G

114031086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43736722-A-G

114031202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43736596-C-G

http://identifiers.org/hco/3/GRCh38#114031486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43736339-C-A

114031486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43736339-C-T

114031507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43736318-A-T

114031572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43736018-C-G

114031572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43736018-C-T

114031573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43736017-T-C

114031609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43735981-G-A

114031609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43735981-G-T

114031696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43735894-T-C

114031740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 43735850-T-C

http://identifiers.org/hco/3/GRCh38#114031843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43735757-C-A

114031848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43735752-T-C

114031855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43735745-G-A

114031855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43735745-G-T

114031931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43735704-T-A

114032625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43731551-A-T

114033212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43731009-C-T

114033273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43730888-T-C

http://identifiers.org/hco/3/GRCh38#114033282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43730879-C-A

114033894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43730266-G-A

114033981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43730189-C-T

114034188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43729989-A-G

http://identifiers.org/hco/3/GRCh38#114034335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43729819-C-A

114034335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43729819-C-T

114034554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43729579-C-T

http://identifiers.org/hco/3/GRCh38#114034747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43729175-C-A

http://identifiers.org/hco/3/GRCh38#114034866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43729059-C-A

114034904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43729021-G-C

http://identifiers.org/hco/3/GRCh38#114035241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43728705-C-A

114035292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43728656-A-G

http://identifiers.org/hco/3/GRCh38#114035417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43728531-C-A

114035507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43728454-C-T

114035931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43728026-G-A

114036687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43727248-T-C

114036687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43727248-T-G

114036823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43727116-T-A

http://identifiers.org/hco/3/GRCh38#114036867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43727085-C-A

114036984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 43726975-A-T

114037051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43726903-A-G

http://identifiers.org/hco/3/GRCh38#114041736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43726419-A-C

114041736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43726419-A-G

http://identifiers.org/hco/3/GRCh38#114041930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43726240-C-A

114041930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43726240-C-T

http://identifiers.org/hco/3/GRCh38#114042709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43725838-A-C

114042778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43725775-C-T

114042868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43725683-T-A

114042932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43725619-A-T

114043478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43725069-A-G

114043581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43724974-C-T

114044776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43720389-G-A

114044776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43720389-G-C

http://identifiers.org/hco/3/GRCh38#114044779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43720386-C-A

114044779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43720386-C-T

114045088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43720083-A-G

114046321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43719154-T-C

114046440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43718741-A-T

114046501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43718683-G-A

114046501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43718683-G-T

114046566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43718617-C-T

114046580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43718603-C-T

114046773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43718410-A-G

http://identifiers.org/hco/3/GRCh38#114047132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43717781-C-A

114047285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43717648-G-T

114048133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43717407-C-G

114048426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43717129-C-T

114048651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43716963-T-G

114048688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43716937-C-T

http://identifiers.org/hco/3/GRCh38#114049177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43716473-A-C

114049295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43716382-C-T

114049628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43715864-A-G

114050805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43715077-G-C

114050965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43714979-T-C

114050990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43714954-G-C

114051716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43714431-C-T

114052409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43713678-C-T

114052854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43713265-T-C

114052863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43713255-G-T

http://identifiers.org/hco/3/GRCh38#114053479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43712646-C-A

http://identifiers.org/hco/3/GRCh38#114053499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43712626-A-C

114053499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43712626-A-G

114053554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43712590-G-C

114053554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43712590-G-T

114053728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43712421-A-G

http://identifiers.org/hco/3/GRCh38#114053818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43712333-C-A

114054002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43712136-A-G

http://identifiers.org/hco/3/GRCh38#114054020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43712122-A-C

114054123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43712028-T-C

114054123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43712028-T-G

114054199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43711934-G-T

114054344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43711797-G-A

114054750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43711934-G-A

114055044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43711766-T-G

114055189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43711616-T-C

114055546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43711262-C-T

114055789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43710964-G-A

http://identifiers.org/hco/3/GRCh38#114055875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43710880-A-C

114055894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43710866-T-C

114055899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43710861-T-C

114055920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43710839-G-C

114055986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43710760-T-C

114056001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43710747-T-A

http://identifiers.org/hco/3/GRCh38#114056053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43710713-C-A

114056237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43710540-G-A

114056237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43710540-G-T

http://identifiers.org/hco/3/GRCh38#114056301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43710475-C-A

114056301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43710475-C-G

114056301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43710475-C-T

114056321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43710455-G-A

114056321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43710455-G-T

114056472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43710302-A-G

114056476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43710298-T-C

114056476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43710298-T-G

http://identifiers.org/hco/3/GRCh38#114056488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43710286-C-A

114056488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43710286-C-T

114056634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron variant
orthologous variants: 43710140-T-G

http://identifiers.org/hco/3/GRCh38#114056736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43710057-C-A

114056736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43710057-C-G

114056736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43710057-C-T

http://identifiers.org/hco/3/GRCh38#114056744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43710049-C-A

http://identifiers.org/hco/3/GRCh38#114056798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#43709987-C-A

114056798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43709987-C-G

114056798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43709987-C-T

114057062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43709770-A-G

114057324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43709528-A-G

114057324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43709528-A-T

114057477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43709411-C-T

114057590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43709308-A-G

114057675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43709222-T-C

114057927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43709006-T-G

114058876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43707680-C-T

114059115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43707438-G-A

114059406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43707092-A-G

114060260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43705564-A-G

114060260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43705564-A-T

114060323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43705498-G-A

114062903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43704611-C-T

114063651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43703608-A-G

114064421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43702467-T-C

114064635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43702038-C-T

114064694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701988-T-G

114064730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701950-A-G

114064870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701828-T-C

http://identifiers.org/hco/3/GRCh38#114065122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43701688-A-C

114065122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701688-A-G

114065122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701688-A-T

114065146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701664-T-A

114065178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701633-A-G

114065178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701633-A-T

114065197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701614-T-C

114065197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701614-T-G

114065212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701599-A-G

114065212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701599-A-T

114065282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43701529-G-C

114065348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43701463-C-G

114065372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43701439-A-G

114065417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43701394-C-T

114065539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701291-T-C

114065563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701272-G-A

http://identifiers.org/hco/3/GRCh38#114065846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43701067-A-C

114065898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701022-C-T

114065933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700996-C-T

114066061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700892-C-G

http://identifiers.org/hco/3/GRCh38#114066088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43700865-A-C

114066088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700865-A-G

114066096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700857-A-G

114066128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700818-G-T

114066131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700815-G-A

114066131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700815-G-T

114066192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700751-A-G

114066201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700742-T-C

http://identifiers.org/hco/3/GRCh38#114066213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43700730-C-A

114066213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700730-C-T

114066316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43700620-A-G

http://identifiers.org/hco/3/GRCh38#114066366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43700571-C-A

114066704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700357-C-T

114067017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700105-A-G

114067017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700105-A-T

114067020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700102-G-A

114067031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700091-A-G

114067109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700010-C-T

114067168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43699972-G-A

114068113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43698271-A-G

114068126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43698260-T-A

http://identifiers.org/hco/3/GRCh38#114068148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43698242-C-A

114068251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43698144-A-G

http://identifiers.org/hco/3/GRCh38#114068270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43698124-C-A

114068270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43698124-C-T

114068438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43697960-A-G

114068493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43697887-C-T

114068554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43697832-G-C

114068583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43697803-G-A

114068583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43697803-G-T

114070513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43697311-A-G

114070539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43697286-G-A

114070539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43697286-G-T

114070556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43697270-T-C

114070857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43696964-C-T

114070872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43696940-G-T

114070964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43696852-T-A

114070984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43696832-A-T

114071055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43696782-T-C

114071122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43696738-T-C

114071123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43696737-A-G

114071701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43696062-C-T

114071947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43695892-C-T

114071997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43695842-G-A

114072101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43695730-C-G

114074056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43694459-G-A

114074579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43694002-G-A

114076833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43692091-C-G

114076833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43692091-C-T

http://identifiers.org/hco/3/GRCh38#114076972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43691952-C-A

114076993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43691932-G-A

114077057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43691874-T-A

114077075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43691858-T-C

114077075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43691858-T-G

114077140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43691812-A-G

114077214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43691743-T-C

http://identifiers.org/hco/3/GRCh38#114077287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43691663-C-A

114077433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43691528-A-G

114077603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43691391-G-T

http://identifiers.org/hco/3/GRCh38#114078184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43690517-C-A

114078352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43690353-T-C

114078539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43690145-T-C

http://identifiers.org/hco/3/GRCh38#114079685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43689668-C-A

114079685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689668-C-G

114079685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689668-C-T

http://identifiers.org/hco/3/GRCh38#114079718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43689635-C-A

114079718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689635-C-T

http://identifiers.org/hco/3/GRCh38#114079740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43689615-C-A

114079740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689615-C-G

114079740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689615-C-T

114079794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689566-A-G

114079799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689561-T-G

114079834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689530-T-G

114079852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689511-G-T

114079865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689499-G-A

114079865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689499-G-C

114079878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43689486-G-A

114079878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43689486-G-T

114079940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43689424-C-T

114079946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43689418-T-G

http://identifiers.org/hco/3/GRCh38#114080119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43689243-C-A

114080275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689097-G-A

114080639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43688725-C-T

114081776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43688484-T-C

114081792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43688468-A-G

114082502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43688065-G-T

114082589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43687975-T-A

114082589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43687975-T-C

114082652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43687912-G-A

114082652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43687912-G-T

114082745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43687820-G-A

114082745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43687820-G-C

114082745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43687820-G-T

http://identifiers.org/hco/3/GRCh38#114082792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43687773-A-C

114082792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 43687773-A-G

114082862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43687705-A-G

114082886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43687676-T-A

114082886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43687676-T-C

http://identifiers.org/hco/3/GRCh38#114082929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43687633-A-C

114082929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43687633-A-G

114082943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43687619-A-G

114082989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43687570-G-A

114082989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43687570-G-C

114082989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43687570-G-T

http://identifiers.org/hco/3/GRCh38#114083048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43687516-C-A

114083752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43684510-T-G

114084030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43684296-A-G

114084668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43684206-T-C

114085601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43683731-G-A

114085637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43683697-G-A

114085637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43683697-G-T

114085857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43683478-G-A

114085916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43683419-T-C

114086036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43683342-T-G

http://identifiers.org/hco/3/GRCh38#114086148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43683242-C-A

114086148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43683242-C-G

114086243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43683160-T-A

114086404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3 prime UTR variant
orthologous variants: 43683008-T-C

114086451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3 prime UTR variant
orthologous variants: 43682967-G-T

114086467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3 prime UTR variant
orthologous variants: 43682951-T-A

114086467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3 prime UTR variant
orthologous variants: 43682951-T-C

http://identifiers.org/hco/3/GRCh38#114086478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43682940-C-A

114086574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3 prime UTR variant
orthologous variants: 43682859-G-A

114086574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3 prime UTR variant
orthologous variants: 43682859-G-T

114086805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3 prime UTR variant
orthologous variants: 43682643-T-C

114086807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3 prime UTR variant
orthologous variants: 43682641-G-A

114087013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3 prime UTR variant
orthologous variants: 43682444-G-T

114088054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3 prime UTR variant
orthologous variants: 43682069-T-C

114088054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3 prime UTR variant
orthologous variants: 43682069-T-G

114088140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3 prime UTR variant
orthologous variants: 43681973-A-G

114088309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25771
most severe consequence: 3 prime UTR variant
orthologous variants: 43681808-A-G