http://identifiers.org/hco/10/GRCh38#118046320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#59931638-C-A

http://identifiers.org/hco/10/GRCh38#118046393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#59931701-A-C

http://identifiers.org/hco/10/GRCh38#118046487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#59931741-C-A

118046487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 59931741-C-G

http://identifiers.org/hco/10/GRCh38#118046579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#59931780-C-A

118046579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 59931780-C-T

118046672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59931844-C-G

118047008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59932166-G-A

118047008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59932166-G-T

118047033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59932193-G-A

118047033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59932193-G-C

http://identifiers.org/hco/10/GRCh38#118047059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59932223-C-A

118047133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59932311-C-T

118047318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59932453-C-T

118047329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59932464-G-A

118047692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59932791-T-C

118048115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59933340-G-T

118048995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59934214-A-G

118049355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59934576-G-A

118049357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59934578-G-A

118049395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59934616-A-G

118049462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59934683-G-A

118049462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59934683-G-T

118050109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59935183-A-G

118050365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59935458-T-C

118050874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59936175-T-C

118051032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59936340-G-C

118051344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59936763-C-T

118051721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59937091-A-G

118051796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59937183-C-G

http://identifiers.org/hco/10/GRCh38#118053720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59937205-C-A

118053751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59937246-G-A

118053751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59937246-G-T

118053848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59937343-C-T

118054029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59937504-C-T

118054031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59937506-G-T

http://identifiers.org/hco/10/GRCh38#118054037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59937512-A-C

118054047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59937547-G-A

http://identifiers.org/hco/10/GRCh38#118054058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59937558-A-C

118054058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59937558-A-G

118054142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59937642-T-C

118054172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59937672-A-G

118054355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59937858-A-G

118054440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59937927-G-A

118054440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59937927-G-T

118054675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59938171-T-C

118054675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59938171-T-G

118055639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59939936-G-T

118055650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59939947-G-T

118055687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59939982-G-T

http://identifiers.org/hco/10/GRCh38#118055837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59940129-C-A

118055886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59940180-A-G

118055937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59940228-G-A

http://identifiers.org/hco/10/GRCh38#118055955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59940245-C-A

118055955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59940245-C-T

118056006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59940292-A-G

118056032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59940318-C-G

http://identifiers.org/hco/10/GRCh38#118056056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59940341-C-A

118056056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59940341-C-T

http://identifiers.org/hco/10/GRCh38#118056057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59940342-C-A

118056057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59940342-C-T

118056061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59940346-C-T

118056090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59940382-G-A

http://identifiers.org/hco/10/GRCh38#118056125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59940450-C-A

118056125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59940450-C-T

118056126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59940451-A-G

http://identifiers.org/hco/10/GRCh38#118056133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59940458-A-C

118056166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59940491-T-C

118056174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59940499-C-G

118056174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59940499-C-T

http://identifiers.org/hco/10/GRCh38#118056199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59940522-C-A

118056199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59940522-C-T

118056300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59941512-C-T

118056568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59941745-A-G

118056678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59941849-A-G

118056678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59941849-A-T

118057220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59942368-G-C

118057439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59942554-G-C

118057478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59942592-C-T

118057495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59942607-A-G

118057548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59942669-C-T

118058181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59943338-A-G

118058971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59944092-G-A

118058971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59944092-G-C

118059032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59944152-G-A

118059373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59946594-G-A

118060312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59947121-T-C

118060406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59947207-G-C

http://identifiers.org/hco/10/GRCh38#118060409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59947210-C-A

118060651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59947444-A-T

118060929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59947727-C-T

118061026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59947819-A-G

118061382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59948101-G-T

118061836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59948615-T-G

118062343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59948939-C-T

http://identifiers.org/hco/10/GRCh38#118062449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59949047-A-C

http://identifiers.org/hco/10/GRCh38#118063032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59950120-A-C

118063065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59950153-G-A

118063066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59950154-A-G

118063544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59950646-A-G

118063719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59950827-T-A

118064051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59951119-G-A

118066713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59953346-A-T

118068553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59953475-G-A

118068553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59953475-G-T

118068616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59953543-G-A

118068616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59953543-G-T

118068844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59954516-T-G

118068859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59954531-A-G

118068859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59954531-A-T

118068871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59954543-G-C

http://identifiers.org/hco/10/GRCh38#118068918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59954589-A-C

118068984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59954642-A-G

118069390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59955005-T-A

118069528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59955170-T-G

118070265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59961825-A-G

118070374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59961972-C-T

118070685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59962384-G-C

118071189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59962915-C-T

http://identifiers.org/hco/10/GRCh38#118071321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59963055-A-C

http://identifiers.org/hco/10/GRCh38#118071622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59963365-A-C

118071910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59963676-G-A

118071987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59963752-G-A

118072203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59964277-T-C

118072244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59964325-T-C

118072352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59964407-T-C

118072522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59964566-A-G

118072690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59964710-C-T

118072720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59964743-A-G

118072834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59964853-G-A

118076456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59967575-T-A

118076457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59967576-T-C

118076540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59967660-T-A

118076540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59967660-T-C

118077082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59967923-C-T

http://identifiers.org/hco/10/GRCh38#118077978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59968660-A-C

118078393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59968739-T-C

118078461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59968789-A-G

118078704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59968986-A-G

http://identifiers.org/hco/10/GRCh38#118078754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59969029-C-A

http://identifiers.org/hco/10/GRCh38#118078926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59969165-C-A

118078926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59969165-C-T

http://identifiers.org/hco/10/GRCh38#118079524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59969423-C-A

http://identifiers.org/hco/10/GRCh38#118079649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59969549-A-C

118080115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59970014-C-T

118080413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59970304-A-G

118080789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59970679-C-T

118081232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59971168-C-T

118081339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59971272-A-G

118081695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59972466-G-A

118081710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59972481-G-A

118082107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59972899-G-C

118082211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59972991-G-A

118082252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59973041-A-G

http://identifiers.org/hco/10/GRCh38#118082495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59973425-C-A

118083465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59974348-A-G

118083693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59974546-G-A

118083734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59974584-T-C

118086939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59976892-T-C

118086953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59976906-A-G

118087096-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59977039-A-T

118088538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59979325-T-C

118088773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59979577-A-G

118088836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59979640-A-G

118088859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59979665-C-T

118089262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59980103-A-G

118089275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59980125-A-T

118089537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59980374-A-G

118090219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59981049-G-T

118090588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59981393-G-T

118090877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59981665-G-A

118091261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59981932-A-G

118091434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59982090-C-T

118092003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59982613-G-C

118092021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59982631-G-T

118092064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59982729-G-A

118092289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59982909-T-G

118093535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59983214-G-A

118093571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59983250-G-A

118093623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59983303-G-A

118093691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59983371-A-G

118093691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59983371-A-T

118094057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59983721-G-T

118096220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59988231-C-G

118096220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59988231-C-T

118096303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59988307-T-C

118096315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59988319-A-G

118096331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59988335-G-A

118096331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59988335-G-T

118096332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59988338-C-T

118097972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59990139-T-C

118098942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59991436-G-A

118098942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59991436-G-T

118099165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59991585-A-G

118099251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59991668-G-A

118099353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59991772-A-G

118099493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59991858-G-A

118099746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59992067-C-T

118099747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59992068-G-A

118099747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59992068-G-T

118099822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59992139-G-T

118100082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59992404-G-A

118100194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59992515-T-C

118100645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59992781-C-T

118100679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59992828-T-G

118100799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59992914-A-G

118100814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59992929-A-G

118100843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59993004-T-C

118101044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59993206-G-C

118101137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59993334-T-G

118101145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59993351-C-T

118101279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59993502-G-C

118101321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59993522-T-C

118101635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59993826-C-T

118101652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59993856-C-T

118101670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59993874-G-A

118101708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59993912-G-T

118101824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59994036-G-A

118102029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59994239-G-A

118102029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59994239-G-C

118102720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59995617-G-A

118102759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59995671-A-G

118102771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59995718-T-G

118102794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59995745-C-T

118103065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59996008-G-A

118103254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59996186-A-G

118103587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59996471-A-G

118103659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59996535-C-T

118104044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59996992-T-C

118104076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59997049-T-C

118104171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59997142-T-C

118104277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59997246-T-C

118104420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59997388-C-G

118104420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59997388-C-T

118104421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59997389-A-T

118104502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59997456-C-T

118104549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59997497-G-A

118104557-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59997503-A-T

http://identifiers.org/hco/10/GRCh38#118104626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59997572-A-C

118104671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59997615-A-T

118104689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59997638-A-G

118104946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59997869-G-A

118105004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59997925-G-C

118105576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59999321-T-G

118105720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59999477-T-G

118106558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60002130-G-A

118106992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60002565-T-G

http://identifiers.org/hco/10/GRCh38#118107314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60002896-C-A

118107818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60003378-T-C

118108152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60003739-C-T

118108229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60003810-C-G

118108251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60003832-C-T

118108258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60003841-C-T

118108367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60003944-C-T

118108477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60004054-G-C

118109224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60004784-C-G

118109267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60004819-G-T

118109347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60004889-G-A

http://identifiers.org/hco/10/GRCh38#118109383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60004911-A-C

118110041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60005466-C-T

118110046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60005471-C-G

118112076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60006153-C-T

118112166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60006244-G-A

118112569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60006638-G-T

118112774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60006827-C-T

118112998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60007032-G-C

118113016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60007044-T-C

118113031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60007059-G-A

118113031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60007059-G-T

118113673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60013620-A-G

118114492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60014414-A-T

118114574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60014476-G-T

118115167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60015336-G-A

118115184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60015353-T-C

118115273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60015438-T-A

118115273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60015438-T-C

118115286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60015451-T-A

118115562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60016702-C-T

118115606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60016725-T-C

118115731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60016846-T-C

118115888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60016988-C-T

118116015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60017116-G-T

118117439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60019323-A-G

118117507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60019383-G-A

118117507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60019383-G-C

118119641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60020625-A-G

118119720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60020689-T-C

118119735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60020700-G-A

118119848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60020809-A-G

118119867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60020828-T-C

118119997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60020945-C-T

118120330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60021239-C-T

118120468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60021357-C-T

118120637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60021535-C-G

http://identifiers.org/hco/10/GRCh38#118121043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60021830-A-C

118121155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60021922-A-G

118121191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60021958-T-A

http://identifiers.org/hco/10/GRCh38#118121356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60022113-C-A

118121364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60022121-T-G

118121421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60024462-C-T

118121539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60024697-G-A

118121623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60024787-A-G

118121652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60024815-G-C

118121687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60024849-G-T

118121963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60025112-T-C

118121999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60025217-C-T

118122244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60026444-G-A

http://identifiers.org/hco/10/GRCh38#118122444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60026652-A-C

118122444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60026652-A-G

118122462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60026669-G-C

118123804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60027861-G-A

118123804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60027861-G-T

118123884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60027943-G-C

118123910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60027954-G-A

118124030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60028059-T-A

118124119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60028320-A-G

118127084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60029299-C-T

118127911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60030414-T-C

118128011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60030491-C-G

118128123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60030538-G-A

118139624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60033083-A-G

118139624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60033083-A-T

118139719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60033650-A-G

118140376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60034236-G-A

118140391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60034254-G-A

http://identifiers.org/hco/10/GRCh38#118140681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60034522-C-A

118140933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60034760-C-T

http://identifiers.org/hco/10/GRCh38#118140947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60034774-A-C

118141233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60035379-C-T

118141362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60035493-A-G

118141842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60035957-C-T

118142039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60036165-C-T

118142091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60036215-G-A

118142282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60036411-G-C

118142459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60037445-T-A

118142459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60037445-T-C

118142468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60037454-T-C

118142511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60037481-G-T

118143988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60038584-G-A

118144162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60038710-G-T

118144255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60038790-G-A

118144620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60038840-G-A

118144972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60039567-A-G

118145000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60039591-G-C

118145318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60039889-T-C

118145365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60039936-T-G

118145401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60039971-G-A

118145420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60039990-A-G

118145563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60040115-C-T

118145635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60040186-G-A

118145761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60040316-C-T

118145835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60040388-G-C

118145924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60040450-G-A

118145924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60040450-G-C

118145941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60040469-G-A

118145954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60040550-C-T

http://identifiers.org/hco/10/GRCh38#118145977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60040573-A-C

118145979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60040575-A-G

118146372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60040916-G-T

http://identifiers.org/hco/10/GRCh38#118146451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60040986-A-C

118146451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60040986-A-G

http://identifiers.org/hco/10/GRCh38#118146709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60041282-C-A

118146784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60041373-G-A

118146787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60041376-G-C

118146930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60041523-A-G

118146987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60041570-G-A

118146987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60041570-G-T

118146988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60041571-C-T

118147065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60041651-T-C

118147231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60042763-T-A

118147231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60042763-T-C

118147947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60043320-G-A

118148213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60043596-G-A

118148285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60043666-T-C

118148763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60044148-C-T

118148896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60044631-G-C

http://identifiers.org/hco/10/GRCh38#118149097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60045223-A-C

118149098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60045224-A-G

118149105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60045231-C-T

http://identifiers.org/hco/10/GRCh38#118149141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60045265-C-A

118149191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60045313-T-C

118149323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60046084-G-C

118149744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60046540-A-G

118149789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60046644-A-G

118149827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60046681-T-C

118150579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60047346-G-A

118150637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60047397-G-A

118150728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60047465-C-T

118150819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60047545-C-G

118150840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60047566-T-C

118152084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60048156-A-G

118152211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60048300-A-G

118157159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60049909-G-A

118157718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60050480-C-T

118159091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60051197-G-A

118159231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60051343-C-T

118159495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60051578-G-A

118159585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60051662-C-T

118159693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60051746-G-C

118159699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60051751-C-T

http://identifiers.org/hco/10/GRCh38#118160930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60052854-C-A

118160930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60052854-C-T

118161088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60053015-G-A

118161179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60053111-C-T

118161202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60053136-G-A

http://identifiers.org/hco/10/GRCh38#118161403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60053316-A-C

118161603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60053533-G-A

118161847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60053753-C-T

118162189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60054089-C-T

http://identifiers.org/hco/10/GRCh38#118162270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60054174-A-C

118162270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60054174-A-G

118162290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60054195-C-T

118166027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60058157-G-A

118166027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60058157-G-C

118166033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60058162-C-T

http://identifiers.org/hco/10/GRCh38#118167271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60059627-A-C

http://identifiers.org/hco/10/GRCh38#118167333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60059690-A-C

118167370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60059731-A-T

118167599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60060082-C-T

118167649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60060129-C-G

118167674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60060154-A-G

118167741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60060551-C-T

118169127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60061394-T-C

118169375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60061612-C-T

118169414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60061635-G-A

118169437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60061659-A-G

http://identifiers.org/hco/10/GRCh38#118169556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60061709-A-C

118169556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60061709-A-T

118170110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60062028-A-G

118170228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60062148-C-T

118170246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60062166-G-A

118170825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60063079-G-A

118170918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60063251-C-T

118171170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60063569-G-A

118171803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60064051-A-G

118171892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60064133-G-A

118171990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60064180-A-G

118173661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60066677-G-C

118174025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60067047-T-C

118174106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60067126-G-A

118174135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60067154-G-A

118174275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60067289-T-A

118174293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60067298-G-A

118181045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60082503-G-A

118181045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60082503-G-C

118181170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60082682-C-T

118181717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60083969-G-A

118181717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60083969-G-T

118181744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60083996-A-G

118181829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60084080-C-T

118181831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60084082-T-C

118181947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60084190-C-T

118182279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60084788-A-T

118182389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60084853-C-T

118182524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60084996-C-T

118182904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60085211-G-A

118182904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60085211-G-T

http://identifiers.org/hco/10/GRCh38#118183071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60085376-C-A

118183116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60085421-A-G

118183699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60086064-A-G

118183918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60086364-G-A

118184333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60086762-C-T

118184661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60087024-G-A

118184676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60087039-G-C

118186742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60088786-T-C

118186756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60088800-G-C

118186882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60088933-C-T

118187557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60089567-T-C

118187854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60089838-T-G

118188146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60090107-A-G

118188319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60090213-A-G

118188538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60090425-G-A

118188538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60090425-G-T

118188682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60090522-A-G

118188941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60090778-G-A

118188941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60090778-G-T

118189010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60090832-G-A

118189032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60090854-G-A

118189488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60091305-A-G

http://identifiers.org/hco/10/GRCh38#118189489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60091306-A-C

118189555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60091355-A-G

118189611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60091408-T-C

118190404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60093155-A-G

118190498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60093246-T-C

118190508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60093256-C-T

118192124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60093365-C-T

118192490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60093681-T-A

118192528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60093720-G-A

118192528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60093720-G-T

118192578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60093770-G-A

118203869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60097001-C-T

118204148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60097141-C-T

118204185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60097168-G-A

118204335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 60097275-C-G

118204347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 60097287-A-G

118204963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 60097937-T-C

http://identifiers.org/hco/10/GRCh38#118205037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60098017-C-A

118205042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 60098022-C-G

118205049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 60098029-A-G

118205178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 60098155-A-G

118205469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60098435-T-C

http://identifiers.org/hco/10/GRCh38#118205478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60098444-C-A

118205598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60098566-G-A

http://identifiers.org/hco/10/GRCh38#118205774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60098729-C-A

118206041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60099008-T-G

118206329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60099306-G-A

http://identifiers.org/hco/10/GRCh38#118206768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60099732-C-A

118206768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 60099732-C-T

http://identifiers.org/hco/10/GRCh38#118206810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60099774-C-A

118207358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 60100312-C-T

118207536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non coding transcript exon variant
orthologous variants: 60100490-G-C

118207536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non coding transcript exon variant
orthologous variants: 60100490-G-T

http://identifiers.org/hco/10/GRCh38#118207638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60100603-C-A

118207763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non coding transcript exon variant
orthologous variants: 60100737-G-A

118207763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non coding transcript exon variant
orthologous variants: 60100737-G-T

118208213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non coding transcript exon variant
orthologous variants: 60101153-T-C

http://identifiers.org/hco/10/GRCh38#118208535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60101451-C-A

118208746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non coding transcript exon variant
orthologous variants: 60101639-G-A

118208905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non coding transcript exon variant
orthologous variants: 60101806-T-C

http://identifiers.org/hco/10/GRCh38#118209169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60102069-C-A

118209169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non coding transcript exon variant
orthologous variants: 60102069-C-G

118209267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non coding transcript exon variant
orthologous variants: 60102164-A-T

http://identifiers.org/hco/10/GRCh38#118209282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60102179-C-A

118209282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non coding transcript exon variant
orthologous variants: 60102179-C-T

118209362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non coding transcript exon variant
orthologous variants: 60102259-T-C

118209367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non coding transcript exon variant
orthologous variants: 60102264-G-A

118209455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non coding transcript exon variant
orthologous variants: 60102342-T-C

118209560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non coding transcript exon variant
orthologous variants: 60102436-G-T

118209734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non coding transcript exon variant
orthologous variants: 60102582-G-A

http://identifiers.org/hco/10/GRCh38#118209828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22933
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#60102660-C-A