83531706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89845031-A-G

83531933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89844806-A-T

83532028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89844711-T-C

83532377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89844371-T-G

83532508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89844250-A-T

http://identifiers.org/hco/5/GRCh38#83533031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89843913-A-C

83533031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89843913-A-G

http://identifiers.org/hco/5/GRCh38#83534912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89843523-A-C

83535318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89843143-G-A

83535366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89843103-T-C

83535535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89842938-C-T

83535595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89842883-C-T

83535785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89842712-G-A

83535785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89842712-G-T

83535810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89842690-G-A

83535810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89842690-G-T

83535855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89842645-G-A

83535855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89842645-G-T

83535861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89842639-G-T

83535893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89842609-G-T

83536057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89842462-G-T

83536138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89842386-T-A

83536147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89842377-A-G

http://identifiers.org/hco/5/GRCh38#83536241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89842283-C-A

83536301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89842223-T-C

83536350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89842169-T-C

83536362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89842157-T-C

83536377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89842142-G-A

83536377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89842142-G-T

83536487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89842042-T-C

83536490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89842039-T-G

http://identifiers.org/hco/5/GRCh38#83536555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89841986-A-C

83536681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89841931-C-T

http://identifiers.org/hco/5/GRCh38#83536696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89841917-C-A

83536696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89841917-C-T

83536794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89841821-A-T

83537166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89841459-A-G

83537249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89841376-C-T

83537273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89841352-C-T

83537423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89841202-A-G

83537470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89841155-A-G

83537523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89841102-A-G

83537621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89841016-G-C

83537779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89840861-A-G

83537779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89840861-A-T

83537792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89840848-G-A

83537915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89840725-A-G

83537915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89840725-A-T

http://identifiers.org/hco/5/GRCh38#83537943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#89840697-A-C

83538011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89840629-A-G

http://identifiers.org/hco/5/GRCh38#83538012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#89840628-C-A

83538012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89840628-C-G

83538150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89840487-C-G

83538150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89840487-C-T

83538154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89840483-T-C

83538185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89840452-G-A

83538223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89840411-A-G

http://identifiers.org/hco/5/GRCh38#83538374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#89840260-C-A

83538458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89840176-G-A

83538789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89839845-C-T

http://identifiers.org/hco/5/GRCh38#83538861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#89839773-C-A

83538861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89839773-C-T

83538871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89839763-G-A

83538881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89839753-G-A

83538924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89839710-T-A

83539001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89839633-C-T

83539017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89839617-C-T

83539194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89839440-C-T

83539415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89839219-A-G

http://identifiers.org/hco/5/GRCh38#83539482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#89839152-C-A

83539482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89839152-C-G

83539535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89839099-G-A

83539583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89839051-A-G

83539583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89839051-A-T

83539630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89839004-T-C

83539630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89839004-T-G

83539755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89838879-T-A

83539755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89838879-T-G

83539791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89838846-T-C

83539792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89838845-A-G

83539797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89838840-C-T

http://identifiers.org/hco/5/GRCh38#83539893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#89838732-A-C

83539944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89838681-T-C

83539987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89838635-C-T

83540019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89838615-C-G

83540037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89838597-C-T

83540068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89838560-C-G

83540068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89838560-C-T

http://identifiers.org/hco/5/GRCh38#83540088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#89838540-C-A

83540134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89838494-A-G

83540402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89838229-A-G

83540443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89838188-T-C

83540631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89837997-T-C

http://identifiers.org/hco/5/GRCh38#83540848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#89837789-C-A

83540848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89837789-C-T

83540880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89837757-C-T

83540931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89837703-T-C

83540955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89837679-A-G

http://identifiers.org/hco/5/GRCh38#83541078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#89837556-C-A

83541078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89837556-C-G

83541228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89837406-G-C

83541491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89837143-A-G

83541498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89837136-A-G

83541553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89837081-A-G

83541553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89837081-A-T

83541555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89837079-G-T

83541562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89837072-C-T

83541637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89836997-A-G

83541682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89836955-T-C

83541698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89836939-G-A

83541741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89836896-T-C

83541812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89836843-G-A

83541812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89836843-G-C

83541812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89836843-G-T

83541869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89836786-G-C

83541869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89836786-G-T

83541969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89836695-G-A

83541969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89836695-G-C

83541969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89836695-G-T

83541988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89836676-T-C

http://identifiers.org/hco/5/GRCh38#83542074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#89836599-C-A

http://identifiers.org/hco/5/GRCh38#83542111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#89836562-A-C

83542144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89836526-C-T

83542312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89836358-A-G

83542337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89836338-G-A

83542479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89836222-T-C

83542673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89836028-A-T

http://identifiers.org/hco/5/GRCh38#83542777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89835931-A-C

83542777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89835931-A-G

83543130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89835572-T-G

83543435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89835241-T-C

http://identifiers.org/hco/5/GRCh38#83543900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89834810-A-C

http://identifiers.org/hco/5/GRCh38#83544391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89834384-A-C

83544522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89834290-A-G

83544577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89834235-A-G

83544697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89834128-C-T

83545093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89833738-A-G

http://identifiers.org/hco/5/GRCh38#83545112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89833719-C-A

83545112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89833719-C-T

83545490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89833353-A-G

83545508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89833335-T-C

83545529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 89833317-T-C

83545629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89833217-A-G

83545680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89833167-G-A

83545701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89833140-T-A

83547645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89832919-G-A

http://identifiers.org/hco/5/GRCh38#83547768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89832807-C-A

http://identifiers.org/hco/5/GRCh38#83547866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89832709-C-A

83547866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89832709-C-G

83547866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89832709-C-T

83547876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89832699-T-C

83547880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89832696-T-C

83547882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89832694-T-A

83547882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89832694-T-C

83547882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89832694-T-G

83547885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89832691-T-C

83547885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89832691-T-G

http://identifiers.org/hco/5/GRCh38#83547907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89832682-C-A

83547907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89832682-C-T

83547916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89832673-G-T

83547955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89832646-T-C

83548206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89832401-G-C

83548206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89832401-G-T

http://identifiers.org/hco/5/GRCh38#83548219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89832387-A-C

83548219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89832387-A-G

83548366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89832241-C-G

83548661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89831964-G-A

83548756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89831900-T-C

83548834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89831821-G-C

83548896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89831762-G-A

83549256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89831230-C-T

83549258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89831228-T-C

83549292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89831194-G-T

83549499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89831033-G-T

83549585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89830942-T-G

83549675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89830862-A-G

83549675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89830862-A-T

83549869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89830677-A-G

http://identifiers.org/hco/5/GRCh38#83549896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89830650-C-A

83550015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89830538-T-C

83550107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89830460-C-G

http://identifiers.org/hco/5/GRCh38#83550159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89830411-C-A

83550159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89830411-C-T

83550215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89830355-A-G

83551538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89829833-A-G

83551588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89829788-G-T

83551662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89829729-T-G

83551957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89829435-C-T

83552195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89829194-G-A

83552204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89829185-T-G

83552220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89829172-G-A

http://identifiers.org/hco/5/GRCh38#83552302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89829062-C-A

83552461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89828905-T-C

83552652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89828766-A-G

83552733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89828700-C-T

83552961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89828484-A-G

83552987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89828457-A-G

83553061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89828387-C-T

83553194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89828245-T-C

83553228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89828212-G-T

83553235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89828205-T-A

83553264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89828176-G-A

83553264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89828176-G-T

83553328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89828112-T-C

83553328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89828112-T-G

83553345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89828096-C-G

83553345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89828096-C-T

83553620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89827823-A-G

http://identifiers.org/hco/5/GRCh38#83553656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89827788-C-A

83553656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89827788-C-G

83553656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89827788-C-T

83553674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89827773-A-G

83553724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89827726-T-C

83553744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89827706-A-G

83553847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89827600-C-G

83554076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89827397-A-G

83554157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89827340-A-T

http://identifiers.org/hco/5/GRCh38#83554810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89826418-C-A

83554810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89826418-C-G

83554810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89826418-C-T

http://identifiers.org/hco/5/GRCh38#83554832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89826379-A-C

83554948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 89826282-T-C

http://identifiers.org/hco/5/GRCh38#83555152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89826119-C-A

83555152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89826119-C-G

83555152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89826119-C-T

83555178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89826093-G-C

83555178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89826093-G-T

83555225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89826044-C-G

83555504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89825784-G-A

83555605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89825660-T-C

83555682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89825465-A-G

83555870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89825275-A-G

83555947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89825192-G-T

83556142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89825029-T-C

83556151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89825020-G-A

83556302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89824929-G-A

83556331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89824901-A-T

83556380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89824855-G-C

83556380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89824855-G-T

83556414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89824820-C-T

83556868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89824356-A-T

83556951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89824284-C-T

83556966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89824266-T-C

83557096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89824141-T-G

83557100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89824137-C-T

83557127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89824092-C-T

83557142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89824077-C-G

83557142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89824077-C-T

83557276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89823875-T-C

83557306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89823840-T-A

83557346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89823783-A-G

83557411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89823677-C-T

83557686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89823300-G-A

http://identifiers.org/hco/5/GRCh38#83557873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89823135-A-C

83557873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89823135-A-G

83558126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89822885-T-C

83558363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89822651-C-T

83558460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89822568-C-T

83558539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89822488-C-T

83558702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89822317-A-G

83558714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89822305-G-A

83558859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89822169-T-C

83558909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89822120-T-A

83558991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89822036-C-T

83559055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89821994-T-C

83559177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89821876-G-A

http://identifiers.org/hco/5/GRCh38#83559223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89821830-A-C

83559304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89821726-T-A

83560775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89820169-C-T

83560789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89820154-G-A

http://identifiers.org/hco/5/GRCh38#83560911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89820000-C-A

83560911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89820000-C-T

83561526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89819394-C-T

83561611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89819306-T-G

http://identifiers.org/hco/5/GRCh38#83561688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89819062-A-C

83561770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89818981-C-T

83561944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89818650-T-C

83561944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89818650-T-G

83561983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89818580-T-C

http://identifiers.org/hco/5/GRCh38#83562174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89818387-C-A

83562188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89818373-T-C

http://identifiers.org/hco/5/GRCh38#83562216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89818343-C-A

83562332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89818236-T-C

83562555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89818024-T-G

83563012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89817586-T-C

83563354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89817280-G-T

83563534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89817088-T-C

83563605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89816980-G-A

83563771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89816815-C-G

83564052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89816566-A-G

http://identifiers.org/hco/5/GRCh38#83564061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89816557-A-C

83564173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89816427-A-G

83564239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89816371-G-T

83564531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89816159-T-G

83564566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89816124-A-G

83564658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89816032-G-T

83564697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89816000-C-T

83564712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89815985-G-A

http://identifiers.org/hco/5/GRCh38#83565140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89815606-A-C

83565148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89815598-C-T

83565210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89815531-A-G

83565212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89815529-A-G

83565816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89814464-C-T

83566654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89813948-C-T

83566768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89813845-G-C

83566949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89813716-G-A

83566966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89813683-T-C

83567051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89813595-A-G

83567126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89813532-A-T

83567168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89813490-A-G

83567755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89813254-T-C

83567902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89812903-G-A

83568177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89812656-C-T

83568445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89812423-C-T

83568672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89812212-T-A

http://identifiers.org/hco/5/GRCh38#83569257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89811752-C-A

83572106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89810468-A-G

83572373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89810218-T-C

83572458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89810136-T-G

83572630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89809975-T-A

83574679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89809558-A-G

83574768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89809467-T-C

83575383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89808912-G-C

83575516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89808795-C-G

83575643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89808678-C-T

83575825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89808486-G-A

83576075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89808282-A-G

83576107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89808252-T-C

83576198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89808187-A-G

83576350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89808056-T-G

83576443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89807968-A-G

83576448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89807962-A-T

83576581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89807829-T-G

83576920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89807504-A-G

83576966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89807459-C-G

83576985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89807440-A-T

83579111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89806373-T-G

83579778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89806017-T-C

83579852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89805948-A-G

83579852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89805948-A-T

83579855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89805944-T-A

83579892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89805895-T-C

83579929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89805853-T-C

http://identifiers.org/hco/5/GRCh38#83579958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#89805824-A-C

83580412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89805370-G-A

83580638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89805146-A-G

83580738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89805049-T-C

83580968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89804814-C-G

83580968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89804814-C-T

http://identifiers.org/hco/5/GRCh38#83581003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#89804781-C-A

http://identifiers.org/hco/5/GRCh38#83581014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#89804770-C-A

http://identifiers.org/hco/5/GRCh38#83581156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40163
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#89804636-A-C