http://identifiers.org/hco/2/GRCh38#112055280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128659955-C-A

http://identifiers.org/hco/2/GRCh38#112055306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128659981-A-C

112055306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 128659981-A-G

http://identifiers.org/hco/2/GRCh38#112055310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128659985-C-A

112055310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 128659985-C-G

112055310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 128659985-C-T

http://identifiers.org/hco/2/GRCh38#112055411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128660085-C-A

112055411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 128660085-C-T

http://identifiers.org/hco/2/GRCh38#112055470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128660131-C-A

112055470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128660131-C-T

112055490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128660151-A-G

http://identifiers.org/hco/2/GRCh38#112055501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128660161-C-A

112055510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 128660170-G-T

http://identifiers.org/hco/2/GRCh38#112055513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128660173-C-A

112055513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 128660173-C-T

112055573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 128660240-G-A

112055580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 128660247-T-C

http://identifiers.org/hco/2/GRCh38#112055631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128660298-C-A

112055631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 128660298-C-T

http://identifiers.org/hco/2/GRCh38#112055672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128660339-C-A

112055672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128660339-C-T

112055678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 128660345-C-T

112055794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128660461-G-A

112055794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128660461-G-C

112055794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128660461-G-T

112055811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128660492-G-A

112055811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128660492-G-T

112055816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128660497-G-A

112055816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128660497-G-T

112055823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128660504-T-C

112055823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128660504-T-G

http://identifiers.org/hco/2/GRCh38#112055843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128660524-C-A

112055843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128660524-C-T

112055874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128660555-T-A

112055874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128660555-T-C

http://identifiers.org/hco/2/GRCh38#112055891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128660572-C-A

112055891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128660572-C-G

112055891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128660572-C-T

112055953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128660629-G-C

112056003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128660682-C-T

112056140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128660830-A-G

112056154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128660843-C-G

112056315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128660952-T-C

112056659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128661249-A-G

112056756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128661335-T-C

http://identifiers.org/hco/2/GRCh38#112057053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128661829-A-C

112057104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128661873-T-C

112057376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128662031-A-G

112057712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128662337-A-G

112057714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128662339-G-A

112058705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128663266-A-G

112058746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128663307-A-T

112058777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128663333-C-T

http://identifiers.org/hco/2/GRCh38#112058821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128663373-A-C

112058822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128663374-T-G

112059049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128663540-A-T

112059128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128663613-C-T

112059455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128663931-C-T

http://identifiers.org/hco/2/GRCh38#112059904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128664927-A-C

112059904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128664927-A-G

112059904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128664927-A-T

112060462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128665144-T-C

112063189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128665566-G-C

112063299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128665647-G-C

112063403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128665763-C-G

112063404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128665764-A-G

112063558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128665836-C-T

112063594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128665867-T-G

112063662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128665895-T-C

112063737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128665962-T-C

112063977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128666166-G-A

http://identifiers.org/hco/2/GRCh38#112064052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128666234-C-A

112064052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128666234-C-G

http://identifiers.org/hco/2/GRCh38#112064054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128666236-C-A

http://identifiers.org/hco/2/GRCh38#112064099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128666281-C-A

112064099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128666281-C-G

112064099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128666281-C-T

112064403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128666578-A-G

112064568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128666897-T-C

112064650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128666971-G-A

112064785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128667043-G-A

112064785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128667043-G-T

112065952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128667227-C-T

112066413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128667653-T-A

112066413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128667653-T-G

112066437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128667685-T-C

112066507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128667759-C-G

112066559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128667802-G-A

112066671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128667907-T-G

112066689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128667925-T-C

112067028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128668269-A-T

112067192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128668346-T-C

112067296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128668444-G-T

112067628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128668638-G-A

112067644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128668654-A-T

http://identifiers.org/hco/2/GRCh38#112067685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128668692-C-A

112067776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128668777-A-G

112074828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128670242-T-C

112075626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128670720-A-T

112076464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128671953-T-A

112076488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128671977-T-C

112076547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128672053-C-T

112076817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128672302-C-T

http://identifiers.org/hco/2/GRCh38#112077181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128672419-C-A

112077181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128672419-C-T

112077251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 128672489-G-A

112077251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 128672489-G-C

112077393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128672611-T-A

112077393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128672611-T-C

112081047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128673091-T-C

http://identifiers.org/hco/2/GRCh38#112081665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128673694-C-A

112081798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128674065-C-T

112081816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128674083-A-G

112081961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128674208-G-C

112082088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128674320-G-A

http://identifiers.org/hco/2/GRCh38#112082119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128674353-A-C

112082445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128674509-C-T

http://identifiers.org/hco/2/GRCh38#112082476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128674537-C-A

112082621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128674670-A-G

112082866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128674980-A-G

112085353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128675409-C-T

112085438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128675464-G-T

112085574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128675603-G-A

112085674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128675763-G-T

112085680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128675769-G-A

112085730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128675806-A-G

112085805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128675875-A-G

112085880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128675945-A-G

112085991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128676021-T-C

112085991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128676021-T-G

http://identifiers.org/hco/2/GRCh38#112085996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128676026-C-A

112085996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128676026-C-G

112085996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128676026-C-T

112086230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128676263-A-G

112086251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128676288-T-C

http://identifiers.org/hco/2/GRCh38#112086254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128676291-C-A

112086254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128676291-C-T

http://identifiers.org/hco/2/GRCh38#112086276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128676313-A-C

112086293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128676330-C-G

112086293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128676330-C-T

http://identifiers.org/hco/2/GRCh38#112088576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128678441-C-A

112088576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128678441-C-T

112088656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128678522-A-G

112088944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128678626-A-G

112088966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128678648-G-A

112088978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128678661-C-T

112088981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128678664-G-A

112089283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128678943-C-T

112089567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128679168-G-T

112089571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128679172-A-G

http://identifiers.org/hco/2/GRCh38#112089581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128679182-C-A

112089604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128679198-G-A

112089604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128679198-G-T

112089757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128679351-G-T

http://identifiers.org/hco/2/GRCh38#112089857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128679456-C-A

112089872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128679471-C-T

112089890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128679487-G-A

112089890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128679487-G-C

112089925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128679517-G-A

http://identifiers.org/hco/2/GRCh38#112089933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128679525-C-A

112089933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128679525-C-T

112090005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128679586-C-G

112090089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128679690-C-T

112090104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128679709-C-T

112090168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128679750-G-A

112090826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128680026-G-A

112091933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128681290-C-T

112092064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128681408-T-C

112094673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128682238-A-T

112094789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128682329-C-G

112094789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128682329-C-T

112094816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128682355-A-G

112094843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128682381-C-T

112095109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128682603-T-C

112097013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128683122-A-T

112097017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128683126-G-T

112097110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 128683221-T-C

http://identifiers.org/hco/2/GRCh38#112097301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128683413-A-C

112097412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128683589-T-G

112097672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128683785-C-T

112098450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128684369-C-T

112098624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128684545-A-G

112098624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128684545-A-T

112098681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128684602-A-G

112098681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128684602-A-T

http://identifiers.org/hco/2/GRCh38#112100499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128687287-C-A

112100499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128687287-C-T

112100575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128687349-A-G

112100578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128687352-A-G

http://identifiers.org/hco/2/GRCh38#112100603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128687362-C-A

112100723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128687503-A-G

http://identifiers.org/hco/2/GRCh38#112100755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128687532-C-A

112100755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128687532-C-G

112100755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128687532-C-T

112100779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128687556-A-G

112100786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128687567-G-T

112105732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128688056-A-G

112105762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128688077-A-T

112105820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128688475-G-C

112105820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128688475-G-T

112105827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128688482-T-C

112105865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 128688519-A-G

112105887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128688545-T-C

112106042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, missense_variant
orthologous variants: 128688689-T-G

112106063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 128688707-T-C

112106267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128688874-A-G

112107612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128690759-G-A

112107648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128690785-G-C

112107648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128690785-G-T

112107677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128690813-A-G

112107741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128690874-G-A

112107741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128690874-G-C

112107741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128690874-G-T

112107784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 128690921-A-G

112107934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128691052-G-A

112107934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128691052-G-C

112107934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128691052-G-T

112112864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128692194-A-G

112113078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128692388-G-T

112113134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128692444-G-C

http://identifiers.org/hco/2/GRCh38#112113204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128692511-A-C

112113226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128692538-G-A

112113335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128692624-G-A

112113335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128692624-G-C

112113384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128692670-G-A

112113385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128692671-T-A

112113565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128692816-G-A

112115993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128693101-A-G

112115993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128693101-A-T

112116043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron variant
orthologous variants: 128693167-G-T

112116076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 128693199-T-C

http://identifiers.org/hco/2/GRCh38#112116081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128693201-C-A

112116081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 128693201-C-T

112116289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128693414-G-C

112116291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128693416-G-T

112116361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128693500-A-G

112116377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128693509-A-G

112116417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128693548-G-A

112116421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128693552-G-A

112116421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128693552-G-T

112116454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128693584-G-C

112116454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128693584-G-T

http://identifiers.org/hco/2/GRCh38#112116523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128693759-C-A

http://identifiers.org/hco/2/GRCh38#112116565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128693798-C-A

112116565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128693798-C-T

112116597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128693815-A-G

112116790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128693964-G-A

112116950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128694097-G-T

http://identifiers.org/hco/2/GRCh38#112117242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128694330-C-A

112117242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128694330-C-T

112117247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128694335-A-G

112117806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128694793-C-T

http://identifiers.org/hco/2/GRCh38#112117828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128694814-C-A

112117984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128694936-G-T

112118237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128695157-A-G

112118315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128695215-G-A

112118315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128695215-G-T

112118332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128695239-T-C

112118375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128695278-G-T

112118376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128695279-G-T

112118393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128695296-C-T

112118396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128695299-T-C

112118414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128695316-G-T

112118415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128695317-G-A

112118415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128695317-G-T

112118431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128695330-G-T

112118437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128695336-A-T

112118500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128695390-T-C

http://identifiers.org/hco/2/GRCh38#112118537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128695432-C-A

112118557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25913
most severe consequence: 3 prime UTR variant
orthologous variants: 128695452-T-G