29650296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607528-G-A

29650296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607528-G-T

http://identifiers.org/hco/7/GRCh38#29650657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24607472-A-C

http://identifiers.org/hco/7/GRCh38#29650724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24607406-C-A

29650790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607343-G-A

29650790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607343-G-T

29650804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607320-A-G

29650829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607295-T-C

29650839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607285-G-A

29650859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607265-G-A

29650859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607265-G-T

29650862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607262-G-A

29650862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607262-G-T

29650870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607238-G-C

29650932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607169-T-C

29651051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607049-G-A

29651051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607049-G-T

29651113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24606982-T-C

29651113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24606982-T-G

29651138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24606945-G-T

29651192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24606899-T-C

29651226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24606833-A-G

29651305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24606777-G-C

29651305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24606777-G-T

http://identifiers.org/hco/7/GRCh38#29651309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24606773-C-A

29651309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24606773-C-G

29651398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24606703-T-C

29651427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24606665-T-C

29651552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24606577-A-T

29651824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24606341-G-C

29651940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24606246-T-C

29652304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24605903-G-C

29652523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24605379-G-A

29652655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24605281-A-G

29652756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24605166-G-A

29653887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24604344-G-A

29654303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603976-A-G

http://identifiers.org/hco/7/GRCh38#29654520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24603789-C-A

29654520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603789-C-T

29654521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603788-G-A

29654686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603602-T-A

29654807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603480-G-A

http://identifiers.org/hco/7/GRCh38#29654922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24603377-C-A

29654994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603317-A-G

29655007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603304-A-G

29655007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603304-A-T

29655014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603297-T-C

29655110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603197-T-C

http://identifiers.org/hco/7/GRCh38#29655164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24603139-C-A

29655164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603139-C-T

http://identifiers.org/hco/7/GRCh38#29655173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24603130-C-A

29655173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603130-C-T

29655195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603108-G-T

29656210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24602439-C-T

29656413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24602261-T-C

29656450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24602229-T-C

29656539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24602150-G-T

29656605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24602089-C-T

http://identifiers.org/hco/7/GRCh38#29656732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24601960-A-C

29656750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601942-A-G

29656756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601936-T-C

http://identifiers.org/hco/7/GRCh38#29656785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24601911-C-A

29656785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601911-C-T

29657280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601513-T-C

http://identifiers.org/hco/7/GRCh38#29657291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24601502-C-A

29657291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601502-C-T

http://identifiers.org/hco/7/GRCh38#29657296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24601499-C-A

29657296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601499-C-T

29657507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601308-A-G

29659677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592642-T-C

29659761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592559-A-G

http://identifiers.org/hco/7/GRCh38#29659837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24592517-C-A

29659837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592517-C-T

29659994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592379-A-G

29660026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592349-C-T

29660071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592319-A-T

29660273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592134-T-A

29660306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24592104-G-A

29660306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24592104-G-C

29660306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24592104-G-T

http://identifiers.org/hco/7/GRCh38#29660336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24592074-A-C

29660505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24591921-G-A

29660505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24591921-G-T

29660531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24591892-G-A

29660531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24591892-G-T

29660533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24591890-G-A

29685851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24582036-T-G

29685982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24581937-C-T

29686021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24581896-G-A

29686078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24581839-C-G

29686078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24581839-C-T

29686890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24581041-G-A

29686967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580974-A-G

29686989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580949-T-C

29687134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580830-T-C

29687217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580753-G-A

29687217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580753-G-T

29687247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580723-T-C

http://identifiers.org/hco/7/GRCh38#29687420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24580564-C-A

29687420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580564-C-T

29687427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580557-T-C

29687428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580556-T-C

29687429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580555-G-A

29687429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580555-G-T

29687454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580527-T-C

29687504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580477-A-T

29687532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580450-G-A

29687532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580450-G-T

29687574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580438-A-G

http://identifiers.org/hco/7/GRCh38#29687613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24580395-A-C

29687613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580395-A-G

29687613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580395-A-T

29687624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580385-T-A

29687624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580385-T-C

29687624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580385-T-G

http://identifiers.org/hco/7/GRCh38#29687632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24580377-C-A

29687632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580377-C-G

29687670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580348-G-A

29687851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580212-T-A

29687854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580209-G-A

29688013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580089-T-A

29688291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579829-G-A

29688316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579804-A-G

29688411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579704-G-A

29688411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579704-G-C

29688461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579656-C-T

http://identifiers.org/hco/7/GRCh38#29688505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24579612-C-A

29688696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579532-G-A

29688700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579528-A-G

29688709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579519-G-A

29688778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579452-T-A

29689093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579192-C-T

http://identifiers.org/hco/7/GRCh38#29689104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24579181-C-A

29689104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579181-C-T

29689149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579140-T-G

29689167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579122-A-T

29689569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578810-G-A

http://identifiers.org/hco/7/GRCh38#29689581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24578781-A-C

29689581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578781-A-G

29689583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578779-A-G

29689594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578768-T-G

29689690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578667-C-T

http://identifiers.org/hco/7/GRCh38#29689702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24578656-C-A

29689981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578445-A-G

29689983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578443-A-G

29690038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578390-A-T

29690158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24578288-G-T

29690280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578184-G-A

29690280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578184-G-T

29691017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24577671-C-T

http://identifiers.org/hco/7/GRCh38#29691027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24577661-A-C

29691074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24577617-C-T

29694381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574662-T-C

29694491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574532-G-A

29694491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574532-G-T

http://identifiers.org/hco/7/GRCh38#29694542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24574484-A-C

29694542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574484-A-G

29694542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574484-A-T

29694611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24574423-T-C

29694689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574346-T-C

29694723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574308-G-A

29694723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574308-G-C

29694723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574308-G-T

29694752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574289-T-C

29694873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574173-G-A

29694879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574167-C-T

29694964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574086-A-G

29695020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574048-A-G

29695029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574039-A-G

29695133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573906-T-G

29695178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573807-T-G

29695278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573485-T-C

29695343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573428-A-G

29695361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573410-A-G

29695361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573410-A-T

29695536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573244-T-G

29696027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573078-G-C

29696091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572998-T-C

29696458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572568-C-T

29696762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572298-G-A

29696827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572239-G-T

29696881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572185-A-G

29697023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24572040-A-G

29697079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571985-T-A

29697089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571975-G-A

29697602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571593-A-G

29697666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571528-A-T

29697725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571460-A-G

29697728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571412-T-C

29697946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571164-C-T

29697966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571145-A-T

29698523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570818-G-A

29698873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570508-C-T

29701168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570068-A-G

29701168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570068-A-T

29702690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24569253-T-A

29704176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557936-T-C

29704359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557747-T-C

29704407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557697-T-C

29704407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557697-T-G

29704408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557696-G-T

http://identifiers.org/hco/7/GRCh38#29704548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24557557-C-A

29704548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557557-C-T

29704559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557549-T-A

29704592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557517-T-C

29704821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557095-A-G

29709738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24555306-T-G

29709886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24555159-G-T

29709914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24555134-T-C

http://identifiers.org/hco/7/GRCh38#29710061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24555017-C-A

29710061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24555017-C-T

29710103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24554978-T-C

29711108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24554914-A-G

29717754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542788-G-C

29717754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542788-G-T

29717782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542757-G-A

29717845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542697-G-A

29717845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542697-G-T

29718054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24542498-G-A

29718276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542271-G-A

29719872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24541275-G-A

29720063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24541127-A-G

29720322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24539682-T-G

29720341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24539666-T-A

29720407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24539595-G-C

29720407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24539595-G-T

29720540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24539470-C-G

29721572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24538677-A-G

http://identifiers.org/hco/7/GRCh38#29722184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24530595-A-C

29722440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24530356-T-C

29722504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24530287-A-G

29722823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24530021-A-G

29722847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529997-T-C

29723006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529859-G-A

29723032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529826-T-A

29723038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529820-T-A

29723044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529814-T-G

29723136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24529737-C-T

29723163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529710-G-A

29723216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529660-T-C

29723220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529656-T-G

http://identifiers.org/hco/7/GRCh38#29723264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#24529612-A-C

29723451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529425-T-G

29723688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529213-G-A

29723704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529197-A-G

29723719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529182-C-T

29724131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528964-T-C

29724176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528872-T-A

29724176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528872-T-C

29724238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528814-T-C

http://identifiers.org/hco/7/GRCh38#29724456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24528599-C-A

29724971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528353-G-T

29725102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528218-G-C

29725337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528103-T-C

29725453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24527973-T-C

29731102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24495010-G-A

http://identifiers.org/hco/7/GRCh38#29731827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24494301-C-A

29731827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24494301-C-T

29731830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24494298-G-A

29731830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24494298-G-C

29731830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24494298-G-T

29731953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: non coding transcript exon variant
orthologous variants: 24494176-G-A

29731953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: non coding transcript exon variant
orthologous variants: 24494176-G-T

29732107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24494019-G-T

29732136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493990-G-A

29732136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493990-G-C

29732136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493990-G-T

http://identifiers.org/hco/7/GRCh38#29732143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24493983-A-C

29732143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493983-A-G

29732399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493668-C-G

29732399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493668-C-T

http://identifiers.org/hco/7/GRCh38#29732531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24493536-A-C

29732582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493487-T-A

29732582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493487-T-C

29732772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493221-T-G

29733304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24492680-A-G

29733508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24492494-A-G

29733713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24492302-A-G

29734167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24491850-G-A

29734389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24491597-C-G

29734685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24491275-T-A

29734856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24491112-A-G

29734993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24490982-C-T

29741410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24470113-T-C

29741636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469964-G-A

29741666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469934-A-G

29741943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469675-T-C

29741985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469634-T-C

29742010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469619-T-C

29742019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469609-T-C

http://identifiers.org/hco/7/GRCh38#29742090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24469528-C-A

29742090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469528-C-T

29742113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469505-A-G

http://identifiers.org/hco/7/GRCh38#29742187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24469441-C-A

29742187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: non coding transcript exon variant
orthologous variants: 24469441-C-G

29742187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: non coding transcript exon variant
orthologous variants: 24469441-C-T

29742193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: non coding transcript exon variant
orthologous variants: 24469435-A-G

http://identifiers.org/hco/7/GRCh38#29742214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24469414-C-A

29742214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: non coding transcript exon variant
orthologous variants: 24469414-C-T

29742278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: non coding transcript exon variant
orthologous variants: 24469348-G-A

29742278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: non coding transcript exon variant
orthologous variants: 24469348-G-T

29742302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: non coding transcript exon variant
orthologous variants: 24469324-A-G

29742473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: non coding transcript exon variant
orthologous variants: 24469149-T-C

29742478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: non coding transcript exon variant
orthologous variants: 24469144-G-A

29742478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: non coding transcript exon variant
orthologous variants: 24469144-G-T

http://identifiers.org/hco/7/GRCh38#29742523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24469112-C-A

29742523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: non coding transcript exon variant
orthologous variants: 24469112-C-G

29742523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: non coding transcript exon variant
orthologous variants: 24469112-C-T

http://identifiers.org/hco/7/GRCh38#29742529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24469106-C-A

29742587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: non coding transcript exon variant
orthologous variants: 24469048-T-C

29742595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22367
most severe consequence: non coding transcript exon variant
orthologous variants: 24469040-G-T