http://identifiers.org/hco/7/GRCh38#34350156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23650819-C-A

http://identifiers.org/hco/7/GRCh38#34350274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23650894-C-A

34350274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: non coding transcript exon variant
orthologous variants: 23650894-C-T

34350356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: non coding transcript exon variant
orthologous variants: 23650971-G-T

http://identifiers.org/hco/7/GRCh38#34350616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23651239-C-A

34350748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: non coding transcript exon variant
orthologous variants: 23651633-A-G

34350810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: non coding transcript exon variant
orthologous variants: 23651693-C-T

34350855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 23651741-C-T

34350876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23651762-G-T

34350939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23651854-A-G

34350951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23651876-G-A

34350951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23651876-G-T

http://identifiers.org/hco/7/GRCh38#34351195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23652105-A-C

34351225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23652141-A-T

34351513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23656755-T-C

34351605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23656908-C-T

34352162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23657155-T-G

34352173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23657166-G-A

34352932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23662134-A-T

34353001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23662232-G-A

34353081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23662294-A-T

34353166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23662371-A-G

34353266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23662477-C-T

34353294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23662503-C-T

34353324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23662533-C-T

34353365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23662575-C-T

http://identifiers.org/hco/7/GRCh38#34353377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23662587-C-A

34353377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23662587-C-G

34353377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23662587-C-T

34354101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23662874-G-A

34354345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23663260-G-A

34354346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23663261-G-A

34354346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23663261-G-C

34354563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23663452-T-G

34354840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23663718-A-G

http://identifiers.org/hco/7/GRCh38#34354955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23663829-C-A

34354956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23663830-A-G

34355223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23664048-G-A

34355239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23664064-G-A

34355272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23664096-G-A

34355298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23664122-C-G

34355321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23664147-G-C

34355328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23664154-A-G

34355367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23664190-C-T

34355459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23664243-G-A

34355554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23664364-C-G

34355554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23664364-C-T

34355764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23664584-A-T

34355793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23664613-C-T

34356037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23664833-C-T

34356315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23665298-A-G

34356332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23665313-C-T

34356477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23665411-C-T

34356721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23665649-C-T

http://identifiers.org/hco/7/GRCh38#34356988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23665892-A-C

34356988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23665892-A-G

34356993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23665897-G-A

34357121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23666019-C-T

34357939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23668127-C-G

34357970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23668157-G-T

34358064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23668258-G-T

34358685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23671303-T-A

34358717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23671336-G-C

34358758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23671370-G-A

34358874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23671486-C-T

34359077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23671696-C-T

34359256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23671812-G-T

34359383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23671940-G-T

34359416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23671973-C-T

34359493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23672055-G-T

34359767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23672317-A-G

http://identifiers.org/hco/7/GRCh38#34359822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23672399-C-A

34359832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23672409-T-C

34359883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23672837-T-C

http://identifiers.org/hco/7/GRCh38#34360012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23672964-A-C

34360130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23673076-C-T

34360195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23673135-C-G

34360298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23671407-C-T

34360377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23671486-C-G

http://identifiers.org/hco/7/GRCh38#34361691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23676258-A-C

34361727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23676288-C-T

34361776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23676321-G-T

34361903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23676444-A-G

34361998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23676523-G-C

34362061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23676585-G-T

34362197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23676722-T-C

34362269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23676787-A-T

34362401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23676911-T-G

34362487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23676987-A-G

34362747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23677239-G-A

34362795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23677276-G-A

34365413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23682666-C-T

34365637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23682880-C-T

34368241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23690988-T-A

34368241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23690988-T-C

34368451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23691300-C-T

34368792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23691613-T-C

34368799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23691620-G-A

34368813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23691636-C-T

34368901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23691706-C-G

34368905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23691710-G-T

34369066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23691868-A-G

34369084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23691889-C-T

http://identifiers.org/hco/7/GRCh38#34369151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23691965-A-C

34369265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23692079-C-G

34369314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23692128-G-T

34369959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23693277-C-T

34370024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23693341-T-C

34370557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23693874-T-A

34370679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23693997-G-A

34370767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23694080-C-T

http://identifiers.org/hco/7/GRCh38#34370824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23694140-A-C

34370849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23694165-T-C

34370894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23694210-G-A

34371161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23694895-C-T

34371207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23694951-T-C

34371317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23695029-A-G

34371336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23695042-A-G

34371439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23695133-T-A

34371439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23695133-T-G

34371573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23695253-A-G

34371693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23695373-T-C

34371745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23695418-A-G

34371762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23695435-T-C

http://identifiers.org/hco/7/GRCh38#34371786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23695459-A-C

34371907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23695549-G-A

34372080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23695728-G-A

34372231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23695907-T-C

34372238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23695920-T-C

http://identifiers.org/hco/7/GRCh38#34372613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23696470-C-A

34372810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23696676-G-T

34372814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23696680-A-G

34372829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23696689-T-C

34372855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23696713-G-A

34372875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23696733-G-C

34372885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23696743-T-C

34372896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23696754-G-A

http://identifiers.org/hco/7/GRCh38#34373076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23696935-A-C

34373130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23696975-G-C

34373251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23697070-G-C

34373454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23697255-T-C

34373764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23697558-G-T

34374073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23697835-A-T

34374086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23697848-G-A

34374525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23698288-C-T

34374603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23698362-A-G

34374635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23698394-T-G

34374648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23698407-G-C

34374717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23698467-G-A

http://identifiers.org/hco/7/GRCh38#34374773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23698525-C-A

http://identifiers.org/hco/7/GRCh38#34374789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23698539-C-A

34374932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23698696-T-C

http://identifiers.org/hco/7/GRCh38#34374943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23698707-C-A

34374943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23698707-C-G

34375001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23698766-A-G

34397270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23703228-G-A

34397295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23703253-G-T

http://identifiers.org/hco/7/GRCh38#34397298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23703269-C-A

34397298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23703269-C-T

34397327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23703302-T-G

34397393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23703365-C-T

34397596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23703540-G-A

http://identifiers.org/hco/7/GRCh38#34397643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23703584-A-C

http://identifiers.org/hco/7/GRCh38#34397696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23703694-C-A

34398074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23704036-T-G

34398241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23705051-C-T

34398284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23705091-C-G

http://identifiers.org/hco/7/GRCh38#34398288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23705095-C-A

34398288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23705095-C-T

34398429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23705229-C-T

34398454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23705254-C-T

http://identifiers.org/hco/7/GRCh38#34398738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23705531-C-A

34399007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23705829-C-T

34399117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23705925-C-T

34399174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23705964-T-C

34399181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23705971-C-T

34399741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23706472-G-A

34399758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23706503-C-T

34399852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23706659-A-G

34399951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23706745-G-A

34399978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23706772-C-G

34399978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23706772-C-T

34401722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23725985-T-G

34401724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23725987-C-T

34401741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23726004-T-A

34401758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23726021-A-G

34401892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23726162-G-C

34402661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23729199-G-A

http://identifiers.org/hco/7/GRCh38#34402718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23729268-A-C

34402718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23729268-A-G

34402718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23729268-A-T

34402735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23729285-G-C

http://identifiers.org/hco/7/GRCh38#34402909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23729447-A-C

34402986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23729512-A-G

34403438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23729914-T-G

34403626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23730115-G-C

34403646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23730135-G-T

34403665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23730154-A-T

34403696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23730184-T-C

http://identifiers.org/hco/7/GRCh38#34404323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23732263-C-A

34404331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23732271-A-G

34404331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23732271-A-T

34404389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23732323-G-C

34404578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23732509-A-G

34405724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23732620-G-A

34405861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23732807-G-A

34405948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23732895-G-A

http://identifiers.org/hco/7/GRCh38#34406097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23733056-C-A

34406981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23733601-G-T

34407563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23734836-T-G

http://identifiers.org/hco/7/GRCh38#34420804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23760147-A-C

34421135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23760514-T-C

34421225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23760600-T-A

34421403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23760768-G-A

34421403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23760768-G-T

34421569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23760932-C-T

34421731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23761087-C-T

http://identifiers.org/hco/7/GRCh38#34421795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23761153-A-C

34421839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23761195-C-T

34422046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23761411-T-C

34422077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23761440-T-A

http://identifiers.org/hco/7/GRCh38#34422175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23761529-A-C

34422374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23761661-C-G

34422569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23761849-G-T

34422857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23762121-A-G

http://identifiers.org/hco/7/GRCh38#34423037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23762257-C-A

http://identifiers.org/hco/7/GRCh38#34423140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23762357-C-A

34424767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23766687-T-C

34424797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23766713-T-C

34425014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23766903-G-A

34425039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23766926-A-T

34425178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23767035-G-A

34425257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23767113-C-G

34425281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23767136-G-C

34425294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23767149-T-C

34425415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23767249-A-G

34425472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23767306-A-G

34425510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23767348-G-C

34425746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23767438-T-C

34425773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23767471-G-C

34425950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23767651-G-A

34426250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23767912-C-T

http://identifiers.org/hco/7/GRCh38#34426274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23767936-A-C

http://identifiers.org/hco/7/GRCh38#34426361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23768023-A-C

34426361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23768023-A-G

34426361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23768023-A-T

http://identifiers.org/hco/7/GRCh38#34426733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23769306-A-C

34426733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23769306-A-T

34426810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23769380-G-A

34426956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23769833-G-C

http://identifiers.org/hco/7/GRCh38#34426989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23769866-C-A

http://identifiers.org/hco/7/GRCh38#34428930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23777650-C-A

34428958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23777679-G-A

http://identifiers.org/hco/7/GRCh38#34429317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23778036-C-A

34429514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23778196-C-T

34429687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23778329-T-C

34430037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23778686-G-A

34430114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23778763-T-G

34430520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23779392-T-C

34430666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23779521-C-T

34430734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23779586-A-G

34430735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23779587-A-G

34474615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23813803-T-G

34474654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23813831-G-T

http://identifiers.org/hco/7/GRCh38#34475022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23814164-C-A

34475069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23814204-A-G

34475071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23814206-A-G

34475100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23814219-C-T

http://identifiers.org/hco/7/GRCh38#34475105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23814224-C-A

34475123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23814241-G-A

34475628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23814906-A-G

34475628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23814906-A-T

34476132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23818174-T-A

http://identifiers.org/hco/7/GRCh38#34476348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23818383-A-C

34476648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23818699-C-T

34476905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23818917-A-G

34477116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23819124-T-C

34477278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23819262-G-A

34477402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23819380-G-C

34479084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23821248-G-T

34479179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23821340-A-G

34479229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23821382-C-T

34479308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23821455-C-T

34479345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23821491-C-T

34479706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23821847-G-T

34479724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23821853-T-C

34479739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23821868-A-G

34479945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23822085-G-A

34480556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23824294-A-G

34480623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23824354-G-A

34480623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23824354-G-T

34481176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23824549-C-T

34481559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23824861-C-T

34481659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23824958-A-G

34481665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23824964-C-G

34481718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23825017-G-A

34481718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23825017-G-C

34481724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23825022-A-G

34481725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23825023-G-A

34481725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23825023-G-C

34481781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23825083-A-T

34481871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23825164-A-G

34481896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23825187-C-T

http://identifiers.org/hco/7/GRCh38#34481919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23825210-A-C

http://identifiers.org/hco/7/GRCh38#34482244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23825508-A-C

34482244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23825508-A-T

http://identifiers.org/hco/7/GRCh38#34482658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23825861-C-A

34482662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23825864-T-C

34483262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23826063-G-A

http://identifiers.org/hco/7/GRCh38#34483278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23826079-C-A

34483510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23826316-A-G

34483554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23826355-C-T

34483635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23826434-A-T

34483649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23826448-G-A

34483649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23826448-G-T

http://identifiers.org/hco/7/GRCh38#34483690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23826482-C-A

34483733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23826506-C-T

34483848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23826723-G-A

34484169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23827032-G-A

34485258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23827725-G-A

34485276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23827743-G-A

34485276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23827743-G-C

34485447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23827845-G-A

34485494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23827884-C-G

34485495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23827885-G-A

34485939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23828394-G-T

34485997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23828430-T-C

34486123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23828539-T-C

34486159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23828573-T-A

34486189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23828603-A-G

34486410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23828819-A-T

http://identifiers.org/hco/7/GRCh38#34486452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23828860-C-A

34486452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23828860-C-T

http://identifiers.org/hco/7/GRCh38#34486471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23828878-A-C

http://identifiers.org/hco/7/GRCh38#34486489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23828896-C-A

34486489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23828896-C-T

34486599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23828996-G-A

34486599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23828996-G-C

34486714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23829106-G-A

34486752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23829137-G-T

34486789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23829169-T-A

34486789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23829169-T-G

http://identifiers.org/hco/7/GRCh38#34487588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23831054-C-A

http://identifiers.org/hco/7/GRCh38#34487589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23831055-C-A

34487589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23831055-C-T

34487641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23831106-A-G

http://identifiers.org/hco/7/GRCh38#34487690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23831152-A-C

34487724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23831176-T-C

34487928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23831394-G-A

34487956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23831422-G-C

34488048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23831514-A-G

34488072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23831533-G-T

34488147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23831593-G-A

34488189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23831622-G-A

34488386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23831775-G-A

34488626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23832016-C-T

34488659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23832058-G-C

34488794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23832192-G-A

34488829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23832227-G-C

34490562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23833127-G-T

34490855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23833399-G-A

34490903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23833428-G-A

34490903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23833428-G-C

34491146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23833588-G-A

34491146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23833588-G-T

34491203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23833645-T-C

34491540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23833971-A-G

34491561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23834041-G-C

34492077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23834249-C-T

34492132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23834302-C-T

34492136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23834306-T-C

34492141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23834309-T-C

34492296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23834427-C-T

34492941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23834952-T-C

http://identifiers.org/hco/7/GRCh38#34493200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23836955-C-A

34493200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23836955-C-T

34493608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23837602-T-C

34493658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23837648-C-T

34496150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23838028-C-T

34496158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23838036-T-G

34496264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23838135-G-A

34496265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23838136-T-C

34496298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23838158-A-T

34496394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23838249-G-A

34496405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23838258-T-C

34496433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23838302-C-T

34496464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23838325-A-G

34496490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23838349-G-C

34496536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23838379-A-G

34496559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23838402-C-T

34496769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23838561-T-A

34496870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23838648-T-C

34496999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23838730-A-G

34497033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23838767-A-G

34497067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23838802-G-T

34497158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23838878-C-T

34497318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23838982-G-A

34497720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23839112-G-C

34497720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23839112-G-T

34497887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23839249-G-A

34498031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23839393-T-C

http://identifiers.org/hco/7/GRCh38#34498148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23839507-C-A

34498163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23839522-C-T

34498217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23839577-G-T

34498355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23839700-A-T

http://identifiers.org/hco/7/GRCh38#34498938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23840425-C-A

34498938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23840425-C-T

34498964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23840449-T-C

34499029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23840512-C-G

34499331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23840842-C-T

34499595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23841105-C-G

34499688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23841160-G-A

34499748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23841209-G-T

34500027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23841462-T-C

http://identifiers.org/hco/7/GRCh38#34500124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23841554-A-C

34500204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23841615-A-G

34500309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23841724-G-A

34500427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23841841-C-T

34500834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23843132-C-T

34500894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23843170-T-C

http://identifiers.org/hco/7/GRCh38#34501058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23843333-C-A

34501129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23843403-C-T

http://identifiers.org/hco/7/GRCh38#34501168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23843443-A-C

34501168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23843443-A-G

34501515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23843804-G-A

34501685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23843941-G-A

34501725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23843982-T-A

34501725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23843982-T-C

34501725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23843982-T-G

34504414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23844459-G-A

34504473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23844521-G-C

34506993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23844629-G-A

34507071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23844707-G-A

34507086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23844722-A-G

34507087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23844723-C-T

34507284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23844897-T-C

34507312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23844923-T-C

34507626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23845232-T-C

34507654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23845257-T-C

34507695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23845286-C-T

34507733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23845323-C-G

34507877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23845440-T-G

34508002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23845561-A-G

34508300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23845831-G-A

34508679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23847448-T-A

34508679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23847448-T-C

34508848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23847612-T-C

34508848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23847612-T-G

34508940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23848491-G-A

34509102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23848671-G-C

34509261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23848809-T-C

34509446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23848997-A-T

http://identifiers.org/hco/7/GRCh38#34509595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23849137-C-A

34509626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23849178-A-T

34511094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23849708-C-G

34511094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23849708-C-T

34511501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23850375-A-T

34551584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23861233-C-T

34551617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23861269-G-A

http://identifiers.org/hco/7/GRCh38#34551752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23861368-A-C

34551862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23861483-G-A

34560984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23867359-T-C

34561015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23867390-A-T

34561162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23867530-G-A

34561172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23867540-T-C

34561275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23867656-T-C

34561555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23867841-A-G

34561634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23867920-A-G

34561672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23867955-T-C

34561673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23867956-T-C

34561728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23868009-C-T

34561794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23868060-C-T

34561849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23868100-C-T

http://identifiers.org/hco/7/GRCh38#34562030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23868279-C-A

34563027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881536-C-T

34563485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881960-T-C

34563831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23884467-T-A

34564052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23884662-A-G

34564177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23884714-G-T

34564616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23885269-T-C

http://identifiers.org/hco/7/GRCh38#34564633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23885286-C-A

34566015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23885668-T-G

34566111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23885769-A-T

34566139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23885797-G-C

34566455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886098-G-C

34566522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886165-C-G

34566522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886165-C-T

34566591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886216-C-T

http://identifiers.org/hco/7/GRCh38#34566659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23886283-C-A

34566659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886283-C-T

http://identifiers.org/hco/7/GRCh38#34566671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23886298-C-A

34566671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886298-C-T

34566684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886310-T-C

34566732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23886349-G-A

34566732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23886349-G-T

34566799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23886411-G-A

34566799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23886411-G-T

34566957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886606-T-C

34566986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886677-T-C

34567020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886749-T-G

34567033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886777-C-T

34567133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23886925-G-T

http://identifiers.org/hco/7/GRCh38#34567151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23886943-C-A

http://identifiers.org/hco/7/GRCh38#34567223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23887005-C-A

http://identifiers.org/hco/7/GRCh38#34567377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23887163-A-C

34567667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23887539-G-A

34567674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23887546-T-C

http://identifiers.org/hco/7/GRCh38#34567738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23887812-A-C

34567870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23887939-G-A

34568014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23888067-G-T

34568037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23888090-T-C

34568157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23888244-G-A

34568157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23888244-G-C

34568157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23888244-G-T

http://identifiers.org/hco/7/GRCh38#34568219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23888305-C-A

http://identifiers.org/hco/7/GRCh38#34568264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23888350-C-A

34568264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23888350-C-T

34568341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23888426-T-A

34568377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 23888488-A-T

34568383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23888494-A-G

34568409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23888528-A-G

34568420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23888539-A-G

34568429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23888548-G-T

34568486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23888726-G-T

34568488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23888728-A-G

34568533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23888759-T-C

http://identifiers.org/hco/7/GRCh38#34568768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23889037-A-C

34568978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23889244-G-A

34569262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

34569283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

34569386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

34569401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

http://identifiers.org/hco/7/GRCh38#34571321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23911318-C-A

34571509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23911484-T-G

34571786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23911713-A-G

34571810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23911731-T-C

34573109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23912832-G-A

34573343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23913057-C-T

34573375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23913088-T-G

34573422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23913134-C-T

34573740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23913545-T-G

34573900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23913700-G-A

34574158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23913932-A-G

34574248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23914019-C-T

34575116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23914867-A-G

34575324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23915071-T-A

34575360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23915109-T-A

34575490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23915242-A-G

34575616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23915359-G-C

34583016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23921102-T-C

http://identifiers.org/hco/7/GRCh38#34583022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23921108-C-A

34583024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23921110-G-T

http://identifiers.org/hco/7/GRCh38#34583273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23921479-A-C

34583370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23921774-T-C

34583558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23922015-G-T

http://identifiers.org/hco/7/GRCh38#34583701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23922152-C-A

34583727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23922177-T-C

34585537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23922312-G-A

34585582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23922357-C-T

34585611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23922386-T-A

http://identifiers.org/hco/7/GRCh38#34585648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23922422-A-C

34585648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23922422-A-T

34585710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23922464-T-C

34586057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23922778-G-A

34586057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23922778-G-T

34586241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23922960-A-G

34586433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23923099-T-C

34588860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23923518-C-T

34588920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23923583-T-C

34589089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23923748-C-T

34589094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23923753-C-T

34589378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23923981-G-A

34589509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23924110-G-A

34589774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23924369-A-G

34589782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23924377-A-G

34592913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23937410-T-C

34592915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23937412-T-C

34592984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23937444-A-G

34593029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23937489-T-C

34593151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23937632-T-G

http://identifiers.org/hco/7/GRCh38#34593266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#23937748-A-C

34593277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23937759-C-T

34593310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23937791-T-C

34593786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23938251-G-C

34593811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23938272-A-G

34594287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23938670-C-G

34594287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23938670-C-T

34594290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23938673-G-A

34597663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23946657-T-A

34597663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23946657-T-C

34597685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23946678-C-T

34597717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23946703-T-C

34597762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23946726-G-A

34597762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23946726-G-C

34597914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23946855-A-G

34598182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23947264-C-T

34598280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23947315-G-A

34598365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23947372-C-T

34598441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23947448-C-T

34598535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23947541-C-G

34598810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23947777-T-C

34599301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23950077-G-A

34599405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23950173-T-C

34599543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23950308-G-A

34599669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23950444-G-A

34599669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23950444-G-T

34599828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22128
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23950676-T-G