73413520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: non coding transcript exon variant
orthologous variants: 99854200-G-T

73413587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: non coding transcript exon variant
orthologous variants: 99854273-T-G

73413621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: non coding transcript exon variant
orthologous variants: 99854307-G-A

73413621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: non coding transcript exon variant
orthologous variants: 99854307-G-T

73413642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 99854324-G-A

http://identifiers.org/hco/13/GRCh38#73413911-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99854597-A-C

73414714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99855364-G-C

73414917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99856044-T-C

73415013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99856161-T-C

73415019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99856167-G-A

73415031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99856177-T-A

73415508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99856662-T-C

73415524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99856678-C-T

http://identifiers.org/hco/13/GRCh38#73415585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99856741-A-C

73415669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99856784-A-G

73416068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99857204-C-G

73416068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99857204-C-T

http://identifiers.org/hco/13/GRCh38#73416382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99857962-A-C

73416563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99858070-G-C

73416582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99858089-T-G

73416592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99858099-G-T

73416763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99858256-C-T

73418272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99859888-C-T

73418291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99859907-T-C

73418331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99859946-A-G

73418467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99860062-G-C

http://identifiers.org/hco/13/GRCh38#73418569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99860158-A-C

73418765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99860344-C-G

73418844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99860425-A-G

73419114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99860657-T-C

73419332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99860863-G-T

73419473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99861001-T-C

73419483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99861011-A-T

73419566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99861087-G-C

73420299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99861338-C-G

73420322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99861359-C-T

73421004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99861431-G-A

73421043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99861470-C-T

73421044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99861471-G-A

73421044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99861471-G-C

73421058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99861484-A-G

73421313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99861895-T-C

http://identifiers.org/hco/13/GRCh38#73421443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#99862020-C-A

73421443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99862020-C-G

73421739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99862306-A-G

73421764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99862331-G-C

73421779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99862346-G-A

73421872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99862439-C-T

73422081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99862658-G-A

73422112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99862689-G-A

73422170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99862745-A-G

73422519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99863185-A-G

73422573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99863237-G-A

http://identifiers.org/hco/13/GRCh38#73423154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99863801-C-A

73423154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99863801-C-G

73426820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99865610-G-A

73426820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99865610-G-T

73426901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99865687-C-T

http://identifiers.org/hco/13/GRCh38#73426913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99865699-C-A

73426929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99865714-T-C

73426960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99865745-A-G

73427232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99865987-G-A

73427433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99866152-A-G

http://identifiers.org/hco/13/GRCh38#73427471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99866191-C-A

http://identifiers.org/hco/13/GRCh38#73427913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99868348-C-A

73427913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99868348-C-T

73427943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99868368-G-C

http://identifiers.org/hco/13/GRCh38#73427957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99868383-A-C

73427981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99868391-G-A

http://identifiers.org/hco/13/GRCh38#73427992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99868402-C-A

73428029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99868429-C-T

73428037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99868437-T-A

73428118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99868514-G-T

73428291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99868695-G-A

73428398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99868802-A-G

73428445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99868849-C-G

73428636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99869085-T-C

73428706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99869159-C-T

73428740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99869198-A-G

http://identifiers.org/hco/13/GRCh38#73428840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99869305-A-C

73429003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99869580-G-A

73429045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99869614-G-A

http://identifiers.org/hco/13/GRCh38#73429086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99869656-A-C

73429086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99869656-A-G

73429453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99869694-G-A

73429453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99869694-G-T

73429483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99869724-A-G

73429750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99869963-T-A

73429750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99869963-T-C

73429876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99870087-C-T

73430015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99870205-G-T

73430979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99873974-A-G

73431264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99874238-C-T

73431284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99874258-G-C

73433249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99874939-G-A

http://identifiers.org/hco/13/GRCh38#73433269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99874960-C-A

73433269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99874960-C-T

http://identifiers.org/hco/13/GRCh38#73433273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99874964-C-A

73433273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99874964-C-G

73433283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99874974-G-A

http://identifiers.org/hco/13/GRCh38#73433314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99875005-C-A

73433381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99875070-C-T

http://identifiers.org/hco/13/GRCh38#73437584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99875414-A-C

73437666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99875495-A-T

73437681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99875549-T-C

73437693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99875564-C-G

http://identifiers.org/hco/13/GRCh38#73437698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99875569-A-C

73437741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99875605-C-T

http://identifiers.org/hco/13/GRCh38#73437745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99875609-A-C

73437745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99875609-A-G

73437829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99875694-T-C

73437835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99875700-G-A

73437975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99875831-C-T

73437994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99875850-T-C

http://identifiers.org/hco/13/GRCh38#73437996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99875852-C-A

73437996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99875852-C-T

73438198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99875967-C-T

73438528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99876208-G-T

73438535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99876215-G-C

73438950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99876787-T-C

73439647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99877357-C-G

73439647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99877357-C-T

73439658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99877368-G-C

73439702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99877403-A-G

73439703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99877404-T-C

73439723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99877424-T-C

http://identifiers.org/hco/13/GRCh38#73439731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99877440-C-A

http://identifiers.org/hco/13/GRCh38#73446645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99878467-C-A

73446645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99878467-C-T

http://identifiers.org/hco/13/GRCh38#73446740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99878557-A-C

73447095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99878981-G-T

73447241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99879117-C-T

73447293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99879158-T-A

73447293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99879158-T-C

73447445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99879326-T-A

73447457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99879338-G-A

http://identifiers.org/hco/13/GRCh38#73447724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99879611-A-C

73447724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99879611-A-G

http://identifiers.org/hco/13/GRCh38#73447830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99879717-C-A

73447943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99879821-G-T

73447978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99879856-T-A

73447978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99879856-T-C

73448310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99880368-G-A

73448310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99880368-G-C

http://identifiers.org/hco/13/GRCh38#73448391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99880501-A-C

73448536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99880682-C-G

73448536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99880682-C-T

73448610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99880807-G-A

73448628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99880824-A-G

73448875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99881035-C-T

http://identifiers.org/hco/13/GRCh38#73449091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99881219-C-A

73449263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99881363-T-A

73449473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99881810-A-G

73449488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99881825-G-A

73449955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99882267-A-G

73449961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99882273-C-T

73450029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99882333-C-T

73450418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99882717-T-C

73450522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99882825-G-T

73450815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99883129-T-C

73450896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99883210-C-T

http://identifiers.org/hco/13/GRCh38#73451008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99883322-C-A

73451008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99883322-C-G

73451142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99883476-G-A

73451646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99883994-C-T

73452409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99884409-T-C

73452769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99884766-C-T

73452934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99885386-G-A

73457428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99886677-A-T

73457464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99886712-G-A

73457614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99893069-G-A

73457614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99893069-G-T

73457626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99893081-G-A

73457646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99893101-A-G

73457717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99893201-G-A

73457717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99893201-G-T

73457862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99893336-A-G

73459432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99893904-G-A

http://identifiers.org/hco/13/GRCh38#73459510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99893982-C-A

73459510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99893982-C-T

73462680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99896573-G-T

73462700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99896593-C-T

73462749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99896643-G-C

73462866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99896741-G-A

73462887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99896762-T-C

73462910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99896788-G-A

http://identifiers.org/hco/13/GRCh38#73462956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99896838-C-A

http://identifiers.org/hco/13/GRCh38#73464217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99897145-C-A

73464217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99897145-C-T

73465127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99897317-G-A

73465272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99897923-G-C

73465396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99898043-T-C

73465423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99898070-A-G

73465565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99898211-C-T

73465638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99898284-G-A

73465842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99898485-C-T

73465858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99898501-T-C

73465932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99898574-T-C

73466194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99898906-G-A

73466230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99898940-T-A

73466231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99898941-C-T

73466437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99899156-T-A

73466437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99899156-T-C

73466446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99899172-C-T

http://identifiers.org/hco/13/GRCh38#73466508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99899228-A-C

http://identifiers.org/hco/13/GRCh38#73466545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99899269-C-A

http://identifiers.org/hco/13/GRCh38#73466593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99899338-C-A

73466676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99899425-A-T

73466899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99899657-T-C

73466930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99899688-G-A

73467009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99899764-C-T

73467065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99899814-G-C

73467115-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99901751-T-A

73467124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99901760-A-G

73467189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99901825-G-A

73467228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99901863-G-A

73467228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99901863-G-C

73467282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99901951-T-C

73467285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99901954-C-T

73467364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902027-G-A

73467371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902034-G-A

http://identifiers.org/hco/13/GRCh38#73467468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99902121-A-C

73467652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902234-C-T

73467687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902269-A-T

73467692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902274-G-A

73467812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902401-C-T

73468390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902724-C-T

73468498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902832-C-T

http://identifiers.org/hco/13/GRCh38#73468715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99903034-C-A

73468715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99903034-C-T

73468721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99903040-A-T

73471321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99903438-C-T

73471384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99903497-A-T

73471643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99903661-A-G

73471702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99903708-C-T

73471714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99903721-G-A

73471722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99903729-A-G

73472220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99903887-C-T

73472387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99904094-G-A

73472478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99904173-T-G

73472681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99904412-G-A

73474758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99905596-C-T

http://identifiers.org/hco/13/GRCh38#73474781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99905614-C-A

73474781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99905614-C-T

73474968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99905838-T-A

73475137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99906001-G-T

73475304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99906164-G-A

73475478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99906297-A-T

http://identifiers.org/hco/13/GRCh38#73475549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99906332-A-C

http://identifiers.org/hco/13/GRCh38#73475994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99907768-C-A

73476060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99907831-G-A

73476248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99908010-G-T

73476671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99908409-G-A

73476795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99908543-C-T

http://identifiers.org/hco/13/GRCh38#73476883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99908631-C-A

73476897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99908645-C-G

73476897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99908645-C-T

73477058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99908784-G-A

73477417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99909341-T-G

73478451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99909604-T-C

73478775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99911174-T-C

73478948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99911328-T-A

73478948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99911328-T-C

73479533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99911859-G-A

73479553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99911879-C-G

73479579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99911905-T-C

73480519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99913233-A-G

http://identifiers.org/hco/13/GRCh38#73480541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99913255-A-C

73480642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99913504-T-C

73481234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99914055-A-G

73481244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99914065-G-T

73481337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99914158-G-A

73481489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99914311-T-G

73481589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99914413-A-T

73481873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99914646-G-T

73481953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99914723-G-A

73481954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99914724-G-C

73482015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99914789-A-T

73483040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99915807-A-G

73483116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99915882-T-C

73483206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99916002-T-C

73483564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99916357-T-C

73483640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99916434-G-A

73484476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99916960-G-T

73484549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99917043-C-G

73484549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99917043-C-T

73484672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99917140-A-T

73484763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99917225-C-T

http://identifiers.org/hco/13/GRCh38#73484795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99917255-C-A

http://identifiers.org/hco/13/GRCh38#73484799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99917259-C-A

73484920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99917365-T-A

73485148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99917557-C-T

73485174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99917582-C-T

73485175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99917583-A-T

73490496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99919682-A-G

73490581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99919756-G-C

73490709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99919873-A-G

73490813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99919995-T-C

http://identifiers.org/hco/13/GRCh38#73490837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99920019-C-A

73490870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99920054-G-A

73490870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99920054-G-T

73490915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99920093-T-C

73491512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99920895-C-T

http://identifiers.org/hco/13/GRCh38#73491815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99921202-C-A

73492116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99921389-G-A

73492122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99921395-A-G

73492269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99921539-G-C

73492518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99922109-C-T

http://identifiers.org/hco/13/GRCh38#73492700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99922328-A-C

73493049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99922674-G-A

73493351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99922972-C-T

73493460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99923073-C-T

73493481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99923094-G-A

73493481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99923094-G-C

73493515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99923132-T-C

73493587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99923172-G-A

73493873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99923418-A-G

73494152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99923906-A-G

73494182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99923936-T-C

73494623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99924363-A-G

73494766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99924506-G-C

http://identifiers.org/hco/13/GRCh38#73495548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99925129-C-A

73495549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99925130-T-C

73495558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99925140-T-A

73495558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99925140-T-C

73495679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99925244-C-G

73496101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99925752-A-G

73496288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99925981-G-T

73496484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99926081-A-T

73496537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99926133-T-G

73496734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99926333-T-G

73497022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99926613-C-T

73500137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99931409-A-G

http://identifiers.org/hco/13/GRCh38#73500306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99931252-A-C

73500306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99931252-A-G

73500562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99931011-G-A

http://identifiers.org/hco/13/GRCh38#73500673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99930896-A-C

73500719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99930850-T-C

http://identifiers.org/hco/13/GRCh38#73501222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99930664-C-A

73501222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99930664-C-G

73501222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99930664-C-T

http://identifiers.org/hco/13/GRCh38#73501306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99930582-A-C

73501392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99930484-G-C

73501516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99930358-G-C

73501693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99930193-G-A

73502121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99929758-G-A

73502121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99929758-G-C

73502270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99929608-A-T

73502850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99929372-C-T

73502851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99929371-T-G

73503000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99929224-G-A

73503020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99929204-A-G

73503020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99929204-A-T

73503214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99929022-A-G

73503642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99931805-T-C

73504077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99932251-T-G

73504186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99932359-G-A

73504311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99932485-C-T

73504340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99932514-C-T

73504439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99932612-G-T

http://identifiers.org/hco/13/GRCh38#73505416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99933097-C-A

http://identifiers.org/hco/13/GRCh38#73505426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99933108-A-C

73505442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99933124-T-G

73505464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99933149-T-G

73505476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99933159-G-A

73508405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99935832-G-A

73508565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99935992-T-A

73508565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99935992-T-C

http://identifiers.org/hco/13/GRCh38#73508571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99935998-A-C

73508667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99936079-A-T

73508677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99936089-T-C

73508911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99936307-G-A

73509203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99936504-G-A

73509203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99936504-G-T

73509356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99936653-T-C

73509413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99936694-T-C

73509414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99936695-G-A

73510499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99938666-G-A

73510658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99938818-T-C

73510745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99938885-C-T

73510904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99939041-C-T

73510918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99939055-G-A

http://identifiers.org/hco/13/GRCh38#73510991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99939795-A-C

http://identifiers.org/hco/13/GRCh38#73511058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99939858-C-A

73511081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99939876-A-G

73511309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99940088-T-C

73511485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99940267-T-G

73511515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99940296-G-A

73511546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99940328-T-C

http://identifiers.org/hco/13/GRCh38#73511553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99940335-C-A

73511553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99940335-C-T

73511577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99940353-T-C

73511592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99940368-G-A

http://identifiers.org/hco/13/GRCh38#73511688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99940467-C-A

73511793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99940588-A-G

73511867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99940657-A-G

73512163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99940914-G-T

73512257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99941008-T-A

73512257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99941008-T-C

73513092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99941308-C-T

73513204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99941389-A-G

73513204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99941389-A-T

73513277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99941482-G-A

73513312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99941514-C-T

http://identifiers.org/hco/13/GRCh38#73513327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99941532-C-A

73513668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99942256-C-T

73513746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99942335-T-C

73513868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99942467-C-T

73513918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99942515-G-A

73513990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99942559-T-A

73513990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99942559-T-G

73514099-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99942669-T-A

73514099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99942669-T-C

73514157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99942723-G-T

73514336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99942880-T-C

73514336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99942880-T-G

73514774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99943259-A-T

73514804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99943289-A-G

73515256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99943714-T-C

73515277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99943739-T-A

73515780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99943941-T-C

http://identifiers.org/hco/13/GRCh38#73515781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99943942-C-A

73515839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99943998-G-T

73515961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99944117-T-C

73516006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99944159-C-T

73516016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99944169-G-A

73516144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99944282-G-A

http://identifiers.org/hco/13/GRCh38#73516182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99944320-A-C

73516240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99944377-T-A

73516501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99945059-C-T

73516590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99945143-C-T

73516619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99945172-G-A

http://identifiers.org/hco/13/GRCh38#73517199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99945864-A-C

73517299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99945965-C-G

http://identifiers.org/hco/13/GRCh38#73517300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99945966-A-C

73517321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99945986-A-G

73518364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99946274-G-A

73519443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99947870-C-T

73520088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99948596-C-G

73520132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99948632-C-T

http://identifiers.org/hco/13/GRCh38#73520146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99948647-C-A

73520716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99948882-G-A

73520727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99948893-A-G

73520924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99949066-G-A

73520979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99949124-G-C

73521147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99949262-T-C

http://identifiers.org/hco/13/GRCh38#73521237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99949334-C-A

73521260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99949363-G-A

73521456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99949557-G-A

73521491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99949578-T-A

73521501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99949586-T-C

73521616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99949700-C-T

73521783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99949877-A-T

73522044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99950161-G-A

73522120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99950233-T-C

73522506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99950626-T-C

73522522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99950642-C-T

73522535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99950662-G-A

73522535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99950662-G-T

73522950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99951158-C-T

73522966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99951190-C-T

73522998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99951221-T-A

73523003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99951226-C-T

73523051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99951269-C-T

73523170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99951380-C-G

73523183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99951393-C-T

73523252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99951443-A-G

73523432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99951701-T-C

73523769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99952046-T-A

73523769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99952046-T-C

http://identifiers.org/hco/13/GRCh38#73523942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99952395-C-A

73524225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99952722-T-C

73524241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99952738-C-T

73524283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99952774-T-C

73524289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99952780-C-T

73524434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99952972-T-C

http://identifiers.org/hco/13/GRCh38#73524487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99953033-C-A

73524487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99953033-C-G

http://identifiers.org/hco/13/GRCh38#73524556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99953100-C-A

73524634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99953166-C-T

http://identifiers.org/hco/13/GRCh38#73524729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99953249-A-C

73524729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99953249-A-G

73524890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99953401-G-A

73525084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99953594-A-G

73525086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99953596-G-C

http://identifiers.org/hco/13/GRCh38#73525114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99953633-C-A

73525258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99953769-A-T

73525284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99953793-G-A

73525645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99954087-A-G

73525650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99954092-T-A

http://identifiers.org/hco/13/GRCh38#73527503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99954352-C-A

73527817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99954751-T-C

http://identifiers.org/hco/13/GRCh38#73527855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99954926-A-C

73528006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99955140-A-T

http://identifiers.org/hco/13/GRCh38#73528017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99955151-A-C

73528073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99955198-C-T

73528221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99955348-G-C

73528586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99955702-A-G

73528639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99955762-T-C

73528999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99955890-A-G

73529252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99957394-C-T

73529898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99957434-G-A

73529956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99957496-T-C

73530174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99957747-C-T

73530284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99957874-G-A

73530322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99957888-T-G

http://identifiers.org/hco/13/GRCh38#73530465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99958029-C-A

73530465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99958029-C-T

73530475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99958039-T-C

http://identifiers.org/hco/13/GRCh38#73531257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99965176-C-A

http://identifiers.org/hco/13/GRCh38#73531500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99965378-A-C

73531500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99965378-A-T

73531572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99965454-G-T

73532222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99966044-T-A

73532247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99966065-G-C

73533013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99967462-G-A

73533161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99967623-A-G

73533401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99967895-T-C

73533677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99968692-A-G

73533881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99968868-C-T

73533970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99968933-G-A

73535341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99969442-T-C

73535494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99969599-G-A

73535646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99969714-G-A

73535779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99969823-A-G

73536183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99970913-A-G

73536261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99970993-C-G

73536261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99970993-C-T

http://identifiers.org/hco/13/GRCh38#73536536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99971251-C-A

73537144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99971862-G-C

73537152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99971870-G-A

73537430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99972151-G-A

73537430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99972151-G-C

73540835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99980102-G-T

73540849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99980117-C-T

73540852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99980120-C-T

73540906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99980168-T-G

http://identifiers.org/hco/13/GRCh38#73541049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99980299-A-C

73541052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99980302-G-T

73541056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99980306-T-C

http://identifiers.org/hco/13/GRCh38#73541225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99980482-C-A

73541500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99980767-G-A

73541500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99980767-G-T

73541529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99980796-A-G

73541563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99980831-T-C

73541644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99980902-G-A

73541807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99981049-T-G

73541851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99981093-C-T

http://identifiers.org/hco/13/GRCh38#73541954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99981116-C-A

73541954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99981116-C-T

73541955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99981117-T-C

73541955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99981117-T-G

73542507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99981379-G-A

73542745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99981624-G-A

73542929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99981805-G-A

73543115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99981966-T-C

http://identifiers.org/hco/13/GRCh38#73543264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99982115-C-A

73544060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99982570-T-G

73544206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99982709-C-G

73544489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99982995-T-C

73544842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99983464-A-G

73545785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99984284-T-C

73545917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99984416-T-C

73545925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99984424-T-C

73545959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99984457-G-A

73545964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99984462-T-A

73546009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99984509-C-G

73546136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99984635-G-C

73546146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99984644-C-T

73546222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99984720-T-C

73546261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99984759-T-C

73546518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99985022-G-A

73546740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99985216-A-G

73546776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99985252-G-A

73546776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99985252-G-T

73546816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99985274-G-A

73546816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99985274-G-T

http://identifiers.org/hco/13/GRCh38#73546818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99985276-C-A

73546818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99985276-C-G

73547006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99985413-C-T

73547332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99985683-T-C

73547645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99986006-G-C

73548369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99986653-C-T

73548467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99986749-G-A

73548467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99986749-G-T

73548485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99986768-T-G

73548609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99986883-T-A

73548610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99986884-G-A

73548625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99986899-C-T

73549327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99987541-A-G

73549446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99987585-G-C

http://identifiers.org/hco/13/GRCh38#73549502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99987610-C-A

73549516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99987623-C-G

http://identifiers.org/hco/13/GRCh38#73549557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99987665-A-C

73549610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99987744-G-T

73549628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99987763-C-T

73549705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99987840-G-A

73549790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99987904-T-C

73549799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99987916-G-A

73549932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99987980-T-A

http://identifiers.org/hco/13/GRCh38#73550005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99988047-C-A

http://identifiers.org/hco/13/GRCh38#73550016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99988058-A-C

73550867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99988749-C-T

73551466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99990851-C-T

73551550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99990936-G-A

73551589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99990975-C-T

73551626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99991021-T-C

73551631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99991026-G-A

73552091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99991475-G-A

73552248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99991630-G-C

73552397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99991759-C-T

73552560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99991876-T-C

73552764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99992071-A-G

73553289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99992492-T-G

http://identifiers.org/hco/13/GRCh38#73553498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99992687-A-C

73554212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99993368-C-T

73554410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99993568-C-T

73555163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99994450-T-C

73555236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99994526-C-G

73555236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99994526-C-T

73555325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99994598-T-G

73555346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99994621-A-G

73555431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99994728-T-C

73555653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99994905-G-C

http://identifiers.org/hco/13/GRCh38#73555777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99995215-A-C

73555901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99995337-C-T

73556126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99995559-A-G

73556353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99995782-G-T

73556559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99995989-G-C

73556895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99996325-T-C

73556907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99996337-C-T

73557029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99996453-T-G

73557152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99996581-G-C

73557192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99996621-T-C

73557192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99996621-T-G

73557239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99996668-G-A

73557291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99996720-G-A

73557307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99996736-G-A

http://identifiers.org/hco/13/GRCh38#73557329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99996754-C-A

http://identifiers.org/hco/13/GRCh38#73557340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99996769-A-C

73557348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99996777-G-A

73557354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99996783-A-G

73557414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99996816-G-T

73557498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99996915-G-A

73557558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99996973-C-T

73557569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99996984-G-A

73557569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99996984-G-C

73557569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99996984-G-T

http://identifiers.org/hco/13/GRCh38#73557576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99996995-C-A

73557720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99997121-A-G

73557754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99997152-C-T

73557808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99997204-T-A

73557862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99997257-T-C

73557934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99997312-A-G

73557941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99997319-T-G

http://identifiers.org/hco/13/GRCh38#73558032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99997428-C-A

73558032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99997428-C-G

73558033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99997429-T-C

73558089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99997485-T-G

73558183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99997568-G-A

73558192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99997577-C-T

73558226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99997619-C-T

73558230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99997623-T-G

73559189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99998406-T-C

73559264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99998473-G-A

http://identifiers.org/hco/13/GRCh38#73559271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99998480-A-C

73559273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99998482-T-C

73559966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99999202-T-G

73559996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99999237-A-T

73560099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99999335-G-A

73560099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99999335-G-C

73560111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99999348-G-C

73560209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99999445-A-T

73560665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99999932-G-A

73560864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100000100-G-T

http://identifiers.org/hco/13/GRCh38#73560976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100000212-A-C

http://identifiers.org/hco/13/GRCh38#73561164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100000273-A-C

http://identifiers.org/hco/13/GRCh38#73561170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100000279-C-A

73562067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100001155-T-C

73562157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100001245-A-G

73562231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100001324-T-A

73562269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100001363-G-C

73562275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100001369-G-T

73562309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100001397-C-T

73562317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100001408-T-C

73562328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100001418-C-G

73562328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100001418-C-T

73562521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100001811-G-A

73562736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100004026-G-A

73562787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100004077-T-C

http://identifiers.org/hco/13/GRCh38#73562790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100004080-A-C

73563088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100004285-C-G

73563490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100005138-C-T

73563520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100005159-C-T

73563562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100005201-T-C

73563824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100005416-T-C

73564005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100005594-T-C

73564243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100005825-T-C

73564277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100005859-G-A

73564277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100005859-G-T

73564287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100005873-A-G

73564294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100005880-G-A

73564409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100005989-A-G

73564457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100006037-T-G

73564529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100006116-G-A

73564605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100006181-C-T

73564657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100006228-C-T

73564833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100006374-C-T

http://identifiers.org/hco/13/GRCh38#73565103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100006625-C-A

73565103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100006625-C-T

73565309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100006880-G-C

73565505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100007074-G-T

73565526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100007095-T-G

73566447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100008820-A-T

73566500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100008873-T-C

73566537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100008908-T-G

73566679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100009040-T-C

73566760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100009119-G-A

73566932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100009318-C-G

73566946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100009332-A-G

73566995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100009357-A-G

73567011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100009372-T-C

73567077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100009437-G-A

73567387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100009612-T-C

73567459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100009670-T-C

73567510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100009723-G-A

73567600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100009798-G-A

73567715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100009918-G-A

73567725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100009928-G-C

73567743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100009946-C-T

73568221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100010428-A-G

73568322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100010509-G-C

73568333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100010529-G-A

73568333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100010529-G-C

73568356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100010552-G-C

73568645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100010824-T-G

73568690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100010861-A-T

73568702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100010872-G-T

73568707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100010877-C-T

73569946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100011560-C-T

73570078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100011690-A-G

73570083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100011695-T-C

73570149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100011756-T-C

73570356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100011942-G-C

73570568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100012155-G-C

73570738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100012313-A-G

73570744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100012319-G-A

73571213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100013116-G-C

http://identifiers.org/hco/13/GRCh38#73571527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100013389-A-C

73572179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100013764-T-C

73572620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100014173-A-G

73572626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100014179-A-G

73572661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100014220-G-A

73572734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100014297-T-G

73573073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100014625-T-G

73573196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100014740-C-T

73573215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100014762-C-T

73573724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100015272-G-C

73573729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100015287-G-C

73573869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100015429-T-C

73573883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100015443-G-A

73573883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100015443-G-T

73573895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100015455-A-G

73574044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100015594-T-C

73574122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100015662-T-C

73576482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100016010-G-T

73576805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100016320-T-C

73576840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100016350-A-G

73576867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100016395-T-C

73576885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100016417-T-A

73576887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100016419-C-T

73576888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100016420-G-A

73576907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100016437-G-A

73576921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100016451-A-G

73576931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100016461-C-G

73577018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100016543-T-G

73577093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100016618-T-C

73577131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100016655-T-C

73577321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100016843-G-C

73577688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100017183-T-A

73577942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100017415-A-T

73578365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100017710-T-C

http://identifiers.org/hco/13/GRCh38#73578546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100017881-C-A

73579042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100019109-T-C

73579356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100019420-T-G

http://identifiers.org/hco/13/GRCh38#73579730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100019796-C-A

73579819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100019947-C-T

73579833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100019969-T-C

73579833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100019969-T-G

73580069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100020437-C-G

73580616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100020909-A-T

73580983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100021236-G-A

73581133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100021373-T-A

http://identifiers.org/hco/13/GRCh38#73581165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100021404-C-A

73581165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100021404-C-T

73581167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100021406-T-C

73581169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100021408-C-T

73581370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100021581-T-A

73581505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100021730-C-T

http://identifiers.org/hco/13/GRCh38#73581920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100022170-A-C

73581997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100022299-T-C

http://identifiers.org/hco/13/GRCh38#73582029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100022345-A-C

73582029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100022345-A-G

73582071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100022381-A-G

73582271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100022589-T-C

73582484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100022812-A-G

73582535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100022866-A-G

73582872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100023319-T-A

73583160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100023596-G-A

73583662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100025441-C-T

73584011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100025765-G-A

73584134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100025868-G-A

73584204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100025932-G-T

73584838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100026613-T-C

73585121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100026891-G-A

73585183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100026945-G-A

73585183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100026945-G-T

73585355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100027134-T-A

73585512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100027293-G-A

73585863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100027633-G-A

73585866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100027636-A-G

73585937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100027716-A-G

73590163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100030263-T-C

73590328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100030426-T-C

73590367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100030464-G-C

73590468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100030566-T-A

http://identifiers.org/hco/13/GRCh38#73590580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100030696-C-A

73590580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100030696-C-T

73590702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100030799-C-T

73590762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100030865-T-C

73590783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100030886-G-C

73590892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100031085-A-G

http://identifiers.org/hco/13/GRCh38#73590913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100031101-C-A

73591232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100032203-C-G

73591983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100033162-A-G

73592487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100034072-A-G

73592564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100034147-C-T

73592617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100034199-A-G

73594433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100035192-C-T

73594438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100035197-T-C

73594502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100035248-G-C

73594529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100035277-C-T

73594632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100035390-C-T

73599913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036735-T-C

73599945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036767-C-T

73599955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036777-G-A

73599977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036806-T-C

73601791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100040324-C-G

73601791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100040324-C-T

73602080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100040592-T-C

73607754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100043125-T-C

73607957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100043384-C-T

73608665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100044048-T-C

73608745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100044129-C-T

73608763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100044147-T-G

73608926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100044300-C-T

73609000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100044374-T-A

73609000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100044374-T-C

73609229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100044619-G-A

73609284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100044673-C-T

73610117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100045690-T-C

http://identifiers.org/hco/13/GRCh38#73610586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100046143-A-C

73610670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100046232-T-G

73610797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100046339-T-G

73610800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100046342-T-C

73610838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100046380-A-G

73611031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100046638-G-A

73611489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100047089-A-T

73611605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100047268-T-G

73618437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100047814-G-A

73618772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100048160-T-C

73618795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100048182-G-A

73618949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100048369-T-C

73619021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100048429-T-A

73619052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100048445-G-C

http://identifiers.org/hco/13/GRCh38#73619059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100048452-A-C

73619059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100048452-A-T

73619112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100048501-T-C

73619223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100048616-G-A

73619372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100048764-A-G

73619381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100048773-T-A

73620574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049063-G-A

73620769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049264-G-A

73620818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049300-A-G

73620937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049420-A-G

73620996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049481-G-C

73621046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049529-G-A

73621093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049608-A-G

73621159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049690-C-T

73621161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049692-G-A

73621291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049822-C-T

73621320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049849-T-C

73621365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049895-T-A

73621656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049943-C-T

73621772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100050063-A-T

73627138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100061799-G-A

73627139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100061800-G-T

73627370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100062013-T-C

http://identifiers.org/hco/13/GRCh38#73632090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100063609-C-A

73632205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100063728-G-A

73632295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100063818-G-C

73632324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100063846-C-T

73632336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100063857-A-G

73632504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100064033-C-G

73632504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100064033-C-T

73632527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100064056-T-C

73632536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100064065-C-T

73633101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100064519-A-T

73633113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100064532-G-T

73633158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100064577-C-T

73633172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100064591-T-C

73633487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100064892-C-T

73633513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100064920-G-A

73633538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100064949-G-A

73633608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100065020-G-A

73633869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100065270-A-T

73634041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100065431-G-T

73634055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100065445-T-A

73634254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100065614-G-A

http://identifiers.org/hco/13/GRCh38#73634435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100065801-A-C

73634475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100065841-T-C

73635364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100067060-A-G

73635392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100067088-C-T

73636789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100067412-G-C

73636861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100068122-T-C

73636930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100068175-G-C

73637095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100068337-G-A

73637239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100068477-G-T

http://identifiers.org/hco/13/GRCh38#73637262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100068502-A-C

73637337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100068574-C-T

73637418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100068654-T-C

73637421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100068657-G-A

http://identifiers.org/hco/13/GRCh38#73637466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100068702-A-C

73637621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100068848-T-C

73637621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100068848-T-G

73638089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100069086-C-T

73638323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100069218-C-G

73638354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100069261-A-G

73638599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100069476-T-C

http://identifiers.org/hco/13/GRCh38#73638765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100069598-C-A

73638808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100069642-G-A

73638963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100069801-T-A

73654833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100071308-C-T

73654967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100071423-C-T

73654968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100071424-G-A

73654990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100071447-T-C

73655101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100071550-G-A

73655210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100071682-G-T

73655365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100071835-T-C

73655436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100071921-C-T

http://identifiers.org/hco/13/GRCh38#73655496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#100071967-C-A

73655496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100071967-C-T

73655625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100072120-G-C

73656146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100072366-T-C

73656172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100072397-G-A

73656199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100072426-G-A

73656199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100072426-G-C

73656328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100072535-G-A