15125308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24806639-G-T

15125335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24806612-G-T

http://identifiers.org/hco/16/GRCh38#15125470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24806506-A-C

15125470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24806506-A-G

15125480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24806496-G-A

15125480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24806496-G-T

15125587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24806385-T-C

15125609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24806363-A-G

15125803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24806155-G-A

15125803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24806155-G-T

15127230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24805802-G-A

15127230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24805802-G-C

15127263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24805743-C-T

15127354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24805654-A-G

http://identifiers.org/hco/16/GRCh38#15127531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24805499-C-A

15127531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24805499-C-T

15127588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24805442-T-A

15127588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24805442-T-C

15127588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24805442-T-G

http://identifiers.org/hco/16/GRCh38#15127885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24805148-A-C

15127886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24805147-G-C

15127886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24805147-G-T

http://identifiers.org/hco/16/GRCh38#15127981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24805049-C-A

15127981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805049-C-G

15127981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805049-C-T

15127987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805043-C-G

15128108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24804922-T-A

15128108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24804922-T-G

15128191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24804843-A-G

http://identifiers.org/hco/16/GRCh38#15128213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24804828-C-A

15128213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24804828-C-G

15128213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24804828-C-T

15128281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24804757-C-T

15128383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24804655-G-A

15128383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24804655-G-C

15128383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24804655-G-T

15128386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24804652-G-A

15128386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24804652-G-C

15128386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24804652-G-T

15129854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800766-G-C

http://identifiers.org/hco/16/GRCh38#15129870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24800742-C-A

15129870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800742-C-T

15129947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24800665-A-T

15130084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24800528-G-A

15130084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24800528-G-C

15130084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24800528-G-T

15130121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800487-T-C

15130248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24800369-C-T

15130269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24800348-G-A

15130465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800154-A-G

15130576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800070-G-A

15130576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800070-G-T

15130849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24799788-C-G

15130885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24799768-G-A

http://identifiers.org/hco/16/GRCh38#15130947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24799683-C-A

15130947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24799683-C-G

15130947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24799683-C-T

15131169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24799465-G-A

15131169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24799465-G-T

15131196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24799438-G-A

15131196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24799438-G-T

15131202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24799432-G-A

15131202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24799432-G-T

15131638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24798996-G-T

15131644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24798990-T-A

15131644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24798990-T-C

15131656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24798978-T-G

15131692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24798942-A-G

15131756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798888-G-T

15131787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798859-G-T

15132643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797999-T-C

15132835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24797818-G-A

15132835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24797818-G-C

15132835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24797818-G-T

http://identifiers.org/hco/16/GRCh38#15133024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24797681-C-A

15133024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24797681-C-G

15133102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797633-T-C

http://identifiers.org/hco/16/GRCh38#15133355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24797419-A-C

15133425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 24797349-T-C

15133425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 24797349-T-G

15133435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797338-G-A

15133435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797338-G-C

15133435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797338-G-T

15133498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24797273-G-A

15133595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24797176-G-C

15133659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24797112-G-A

15133659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24797112-G-C

15133659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24797112-G-T

15133892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24796904-G-A

15133892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24796904-G-T

15134016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24796780-G-T

15134095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24796692-G-A

15134095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24796692-G-T

15134096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24796691-A-G

http://identifiers.org/hco/16/GRCh38#15134215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24796621-C-A

15134215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24796621-C-G

15134215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24796621-C-T

15134625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796282-G-A

15134625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796282-G-T

15134737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796186-G-A

15134799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796137-A-G

15134833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796126-C-T

15134840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796119-C-G

15134840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796119-C-T

http://identifiers.org/hco/16/GRCh38#15134861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24796091-C-A

15134861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796091-C-T

15134894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796053-G-T

http://identifiers.org/hco/16/GRCh38#15134962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24795987-C-A

15134962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24795987-C-T

15134995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24795954-G-C

15135923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24794941-G-A

15135923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24794941-G-C

15135923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24794941-G-T

15136013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24786214-G-C

15136013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24786214-G-T

http://identifiers.org/hco/16/GRCh38#15136067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24786160-C-A

15136067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24786160-C-T

http://identifiers.org/hco/16/GRCh38#15136084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24786146-A-C

15136084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24786146-A-G

15136084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24786146-A-T

15136367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785135-G-A

15136388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785113-C-T

15136493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785020-C-T

15136500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785013-G-A

15136500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785013-G-C

15136500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785013-G-T

15136505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785006-C-T

15136514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784996-A-G

http://identifiers.org/hco/16/GRCh38#15136533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24784974-A-C

15136533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784974-A-G

15136647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24784862-C-G

15136647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24784862-C-T

http://identifiers.org/hco/16/GRCh38#15136962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24784561-C-A

15136962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24784561-C-T

15137018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24784505-T-A

http://identifiers.org/hco/16/GRCh38#15137046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24784477-C-A

15137046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24784477-C-T

15137171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24784352-A-G

15137258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24784265-G-A

15137258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24784265-G-T

15137267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24784256-A-G

15137500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24784023-G-T

http://identifiers.org/hco/16/GRCh38#15137584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24783935-C-A

15137584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783935-C-G

15137584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783935-C-T

15137616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783882-A-G

15137624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783874-G-A

15137624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783874-G-C

15137624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783874-G-T

http://identifiers.org/hco/16/GRCh38#15137669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24783831-C-A

15138156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783417-T-C

15138156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783417-T-G

15138162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783411-C-G

15138162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783411-C-T

15138386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 24783192-G-A

15138462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24783116-G-A

15138462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24783116-G-C

15138484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783098-G-C

15138484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783098-G-T

15141890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24780524-C-G

http://identifiers.org/hco/16/GRCh38#15141902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24780512-C-A

15141902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24780512-C-T

15141905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24780509-T-C

http://identifiers.org/hco/16/GRCh38#15142242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24780215-C-A

15142559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24780012-G-A

15142559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24780012-G-C

15142699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24779878-G-C

15142740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24779854-C-T

15142806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24779799-C-T

15142815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24779790-C-T

15144068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24778138-C-T

http://identifiers.org/hco/16/GRCh38#15144069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24778137-A-C

15144071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24778135-G-A

15144152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24778043-G-A

15144330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24777818-G-A

15144330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24777818-G-C

15144496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24777636-G-A

15144513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24777586-T-C

http://identifiers.org/hco/16/GRCh38#15144719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24777316-C-A

15144934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24777098-G-C

15144993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24777015-T-G

15145218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24776865-G-A

15145519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24776572-G-T

15145545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24776560-A-G

15145557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24776548-G-A

15145599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24776505-A-G

15145854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24776230-C-T

15145928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24776132-T-C

15146016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24776023-G-A

http://identifiers.org/hco/16/GRCh38#15146030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24776009-A-C

http://identifiers.org/hco/16/GRCh38#15151676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24771995-A-C

15151676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24771995-A-T

15152057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24771587-G-A

15152092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24771557-C-T

15152195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24771464-C-T

15152197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24771462-G-C

15152197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24771462-G-T

15152313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24771382-G-A

15153006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24770812-G-C

15153006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24770812-G-T

15153012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24770806-G-A

15153390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24770375-G-A

15153410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24770355-G-T

http://identifiers.org/hco/16/GRCh38#15153496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24770301-C-A

15153683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24770120-G-C

15153683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24770120-G-T

15153892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24769983-T-C

15153898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24769977-C-T

15154093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24769810-C-T

http://identifiers.org/hco/16/GRCh38#15154102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24769801-C-A

15154102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24769801-C-T

15154131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24769770-T-C

15154176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24769720-C-G

15154176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24769720-C-T

15154265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24769629-C-G

15154265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24769629-C-T

15154555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30070
most severe consequence: non coding transcript exon variant
orthologous variants: 24769244-C-T