87130129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144107383-G-A

87130129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144107383-G-T

87130322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144107219-C-T

87130540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144107045-C-T

87130822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144106779-C-T

87131736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144105884-A-G

87131849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144105754-T-G

87132002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 144105617-C-T

87132021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 144105604-T-G

87132087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 144105564-T-G

87132113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 144105538-G-A

http://identifiers.org/hco/1/GRCh38#87132182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144105480-C-A

87132182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144105480-C-T

87132679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144105007-T-A

87132686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144105000-C-G

87132686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144105000-C-T

87132694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104992-G-A

87132704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104936-C-G

87132797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104835-G-A

87132797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104835-G-T

87132924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104700-G-A

87132924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104700-G-C

87132933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104686-A-G

87132966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104656-T-C

87132969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104653-G-A

87132969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104653-G-T

http://identifiers.org/hco/1/GRCh38#87132979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144104648-C-A

87132979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104648-C-T

http://identifiers.org/hco/1/GRCh38#87132995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144104633-C-A

87133009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104619-G-T

87133081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104535-A-G

87133081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104535-A-T

http://identifiers.org/hco/1/GRCh38#87133118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144104512-C-A

87133118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104512-C-T

87133150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104491-G-A

87133150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104491-G-T

http://identifiers.org/hco/1/GRCh38#87133174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144104464-C-A

87133174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104464-C-T

http://identifiers.org/hco/1/GRCh38#87133211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144104445-C-A

http://identifiers.org/hco/1/GRCh38#87133372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144104308-C-A

87133372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104308-C-T

87133392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104288-G-T

87133465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104262-G-C

87133465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104262-G-T

87133467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104260-G-A

87133467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104260-G-T

http://identifiers.org/hco/1/GRCh38#87133513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144104251-A-C

87133513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104251-A-G

87133513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104251-A-T

87133521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104243-G-A

87133521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104243-G-T

http://identifiers.org/hco/1/GRCh38#87133557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144104215-C-A

87133557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144104215-C-T

http://identifiers.org/hco/1/GRCh38#87133668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144104096-C-A

87133668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144104096-C-T

http://identifiers.org/hco/1/GRCh38#87133866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144103951-A-C

87133874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103943-C-T

87133894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103923-A-G

http://identifiers.org/hco/1/GRCh38#87134028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144103850-C-A

87134028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103850-C-T

87134129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103748-G-C

87134239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103641-C-T

87134249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103625-G-A

87134249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103625-G-T

http://identifiers.org/hco/1/GRCh38#87134259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144103615-C-A

87134264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103610-G-A

87134264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103610-G-T

87134296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103597-C-T

87134302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103591-G-C

87134302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103591-G-T

87134335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103575-G-A

87134335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103575-G-T

87134348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103562-T-C

http://identifiers.org/hco/1/GRCh38#87134369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144103541-A-C

http://identifiers.org/hco/1/GRCh38#87134390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144103519-A-C

87134393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103516-C-T

87134716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103213-T-A

87134716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103213-T-C

87134840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103099-T-C

87134865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103072-C-T

87134904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103033-G-C

87134913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144103020-G-A

87135298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144102638-A-G

87135559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144102373-T-A

87135572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144102360-G-T

87135584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144102350-A-G

http://identifiers.org/hco/1/GRCh38#87135641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144102285-C-A

87135641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144102285-C-T

87135657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144102253-T-A

87135657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144102253-T-C

87135671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144102232-A-G

87135726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144102175-G-A

87135928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144101964-C-T

87135978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144101926-C-T

87136101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144101817-G-T

87136110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144101808-T-C

87136220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144101697-G-A

87136249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144101668-T-C

87136734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144101181-G-T

87136736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144101179-A-T

87137185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144100731-A-G

87137416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144100517-A-G

87137506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144100428-G-A

87137617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144100326-A-G

87137664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144100154-A-G

87137773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144099967-G-A

87137773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144099967-G-T

87137806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144099938-C-T

87137896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144099847-G-A

87138391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144099403-G-A

87138565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144099264-T-A

87138699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144099190-G-A

87138764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144099128-T-A

87138802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144099093-A-G

87139054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144098839-G-A

87139058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144098835-G-A

87141351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144097043-G-C

87142380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144095971-G-A

87142681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144095669-G-A

87142753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144095597-C-T

87142785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144095565-T-C

87142916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144095446-T-C

87143040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144095349-C-T

87143611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144095096-A-G

http://identifiers.org/hco/1/GRCh38#87143648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144095060-C-A

87143671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144095033-G-A

http://identifiers.org/hco/1/GRCh38#87145037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144093634-A-C

87145102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144093562-G-A

87145102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144093562-G-T

http://identifiers.org/hco/1/GRCh38#87146160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144092629-C-A

87146160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144092629-C-T

87146163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144092626-T-G

http://identifiers.org/hco/1/GRCh38#87146246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144092536-A-C

87146469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144092315-A-G

87146514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144092273-G-T

87147281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144091615-T-A

87147281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144091615-T-G

http://identifiers.org/hco/1/GRCh38#87147322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144091570-A-C

87147322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144091570-A-T

87147373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144091552-T-A

87147373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144091552-T-G

87147441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144091488-G-A

87147482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144091384-A-G

87147499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144091367-G-A

87147504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144091362-G-T

87147620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144091193-T-C

87147756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144090955-A-G

87147769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144090943-G-A

87147898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144090844-G-A

87148115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144090642-T-G

87148140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144090616-G-A

87148255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144090504-T-C

87148291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144090487-G-A

http://identifiers.org/hco/1/GRCh38#87148377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144090406-A-C

87148377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144090406-A-T

87148434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144090348-G-T

87148492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144090304-G-A

87148658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144090185-C-G

87149041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144089894-C-G

87149041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144089894-C-T

87149066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144089880-C-T

87149102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144089825-G-A

87149352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144089631-C-G

87149407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144089586-G-A

87149609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144089407-T-C

87149706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144089274-C-T

87149933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144089067-T-A

87149948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144089052-C-T

http://identifiers.org/hco/1/GRCh38#87150055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144088961-A-C

87150125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144088893-G-T

87150306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144088694-A-G

87151053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144087863-A-T

87151200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144087714-A-G

87151339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144087587-A-G

87151347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144087578-T-C

87151793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144087181-T-C

87151919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144087054-C-G

87152067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144086935-G-A

87152109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144086894-C-T

87152129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144086872-G-T

87152255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144086804-G-C

87152951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144085996-T-A

87153162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144085786-G-A

87154167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144085125-A-G

87154383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144084950-A-G

87154522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144084828-G-A

http://identifiers.org/hco/1/GRCh38#87154525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144084825-A-C

87154525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144084825-A-T

87155542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144083839-G-A

87155731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144083638-C-T

87155964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144083406-T-C

http://identifiers.org/hco/1/GRCh38#87156374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144082996-A-C

87156732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144082654-G-A

87157019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144082384-C-T

http://identifiers.org/hco/1/GRCh38#87157080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144082326-C-A

87157095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144082311-G-A

87157202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144082200-A-G

87157202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144082200-A-T

87157265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144082118-A-G

http://identifiers.org/hco/1/GRCh38#87157352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144082029-C-A

http://identifiers.org/hco/1/GRCh38#87157556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144081829-A-C

87157804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144081581-T-C

87158125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144081145-G-A

87158312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144080701-T-A

87158312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144080701-T-C

87158336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144080655-C-T

87158515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144080512-G-A

87158515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144080512-G-T

87158540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144080489-C-T

87158580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144080445-G-A

87159010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144079953-T-C

87159010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144079953-T-G

87159175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144079796-G-A

87159175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144079796-G-C

87159195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144079777-A-G

87159270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144079702-A-G

87159295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144079673-C-G

87159437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144079530-T-C

87159527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144079441-G-A

87159533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144079435-G-A

http://identifiers.org/hco/1/GRCh38#87159655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144079390-A-C

87159669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144079376-T-C

87159684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144079360-G-A

87159819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144079219-T-C

87159891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144079143-G-C

87162734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144078276-T-A

87162754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144078257-T-C

87162788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144078221-A-G

http://identifiers.org/hco/1/GRCh38#87162969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144078051-C-A

87162969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144078051-C-T

87163023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144078004-G-A

87163023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144078004-G-C

87163023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144078004-G-T

87163151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144077902-T-C

87163627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144077428-G-A

87163688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144077370-T-C

87163696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144077362-C-T

87163893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144077257-C-G

87164212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144077030-T-C

87164243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144077000-C-T

87164684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144076565-C-G

87164684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144076565-C-T

87164696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144076553-T-A

87164936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144076333-C-G

http://identifiers.org/hco/1/GRCh38#87165390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144075869-C-A

87165398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144075861-T-C

87165401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144075858-C-T

http://identifiers.org/hco/1/GRCh38#87165829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144075453-C-A

http://identifiers.org/hco/1/GRCh38#87166692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144074973-C-A

87166695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144074970-C-T

87166698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144074967-A-G

87166739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144074925-A-G

87167031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144074632-G-C

http://identifiers.org/hco/1/GRCh38#87167412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144074322-C-A

87167412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144074322-C-G

87167464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144074280-A-G

87167532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144074197-C-G

http://identifiers.org/hco/1/GRCh38#87167717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144074012-A-C

87167783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144073948-T-G

http://identifiers.org/hco/1/GRCh38#87168058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144073732-C-A

87168058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144073732-C-T

http://identifiers.org/hco/1/GRCh38#87168127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144073663-C-A

87168127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144073663-C-G

87168127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144073663-C-T

87168129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 144073661-T-C

87168134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non_coding_transcript_variant, undefined
orthologous variants: 144073656-A-G

87168134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non_coding_transcript_variant, undefined
orthologous variants: 144073656-A-T

http://identifiers.org/hco/1/GRCh38#87168144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144073646-A-C

87168144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144073646-A-G

87168168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144073622-G-A

87168168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144073622-G-C

87168168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144073622-G-T

87168187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144073603-A-G

87168188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144073602-A-G

http://identifiers.org/hco/1/GRCh38#87168242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144073548-C-A

http://identifiers.org/hco/1/GRCh38#87168282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144073508-C-A

http://identifiers.org/hco/1/GRCh38#87168283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144073507-C-A

87168410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144073373-A-G

87168437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144073346-G-A

87168437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144073346-G-T

http://identifiers.org/hco/1/GRCh38#87168439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144073344-C-A

87168439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144073344-C-T

http://identifiers.org/hco/1/GRCh38#87168469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144073314-C-A

87168469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144073314-C-T

87168497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144073283-T-G

87168519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144073261-A-G

87168522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144073258-G-C

87168526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144073255-C-T

87168555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144073226-G-A

87168555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144073226-G-T

87168626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144073154-T-C

87168646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144073134-A-G

http://identifiers.org/hco/1/GRCh38#87168648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144073132-C-A

http://identifiers.org/hco/1/GRCh38#87168792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144072989-C-A

http://identifiers.org/hco/1/GRCh38#87169021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144072724-C-A

87169021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144072724-C-G

87169041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144072704-T-C

87169078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144072667-A-G

87169141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27922
most severe consequence: non coding transcript exon variant
orthologous variants: 144072603-G-C