21384357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88509675-G-T

21384397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88509722-T-C

21384555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88509864-T-C

21384555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88509864-T-G

21384734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510021-T-C

21384793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510083-G-A

21384793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510083-G-C

21384817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510107-C-T

21384819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510109-T-C

21384853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510143-G-T

21384881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510171-G-A

21384881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510171-G-C

21384881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510171-G-T

21384887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510177-C-G

21384895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510185-G-A

21384895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510185-G-C

21384906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510196-C-T

21384914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510204-A-G

21384931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510221-C-G

21384931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510221-C-T

21384943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510233-T-G

21384945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510235-T-C

21384946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510236-C-T

http://identifiers.org/hco/9/GRCh38#21384948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88510238-C-A

21384948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510238-C-G

21384950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510240-C-G

http://identifiers.org/hco/9/GRCh38#21384952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88510242-C-A

21384952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510242-C-T

21384956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510246-C-T

http://identifiers.org/hco/9/GRCh38#21384957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88510247-C-A

21384957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510247-C-G

21384957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510247-C-T

21385001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510291-T-A

21385004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510294-G-T

21385009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510299-G-A

21385032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510322-C-T

21385048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510338-G-A

21385065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510355-G-C

21385067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510357-T-C

21385074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510364-T-C

http://identifiers.org/hco/9/GRCh38#21385090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88510380-A-C

21385090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510380-A-G

21385090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510380-A-T

21385091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510381-T-A

21385091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510381-T-C

21385093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510383-G-C

21385116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510406-T-A

21385134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510427-A-G

21385137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510430-C-T

http://identifiers.org/hco/9/GRCh38#21385138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88510431-C-A

21385138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510431-C-T

21385140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510433-C-T

21385144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510437-G-A

21385144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510437-G-C

21385180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510473-G-A

21385205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510498-G-T

21385216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510509-C-T

21385237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510530-G-A

21385246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510539-T-C

21385252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510545-C-G

21385252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510545-C-T

http://identifiers.org/hco/9/GRCh38#21385293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88510586-C-A

21385293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510586-C-T

21385300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510593-G-A

21385305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510598-C-T

21385318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510611-G-A

21385318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510611-G-T

21385344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510637-A-G

21385344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510637-A-T

21385488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88510782-T-G

http://identifiers.org/hco/9/GRCh38#21385531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88510824-C-A

21385531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88510824-C-G

21385596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88510894-T-C

http://identifiers.org/hco/9/GRCh38#21398177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88739110-A-C

http://identifiers.org/hco/9/GRCh38#21398283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88739027-A-C

21398387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88738936-T-C

21398387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88738936-T-G

21398398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88738925-A-G

21398464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88738877-C-T

21398552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88738814-A-G

21398570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88738796-G-A

21398572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88738794-G-T

http://identifiers.org/hco/9/GRCh38#21398576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88738792-C-A

21398576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88738792-C-T

21398589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88738779-T-A

21398629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738743-T-C

21398639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738736-C-G

21398639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738736-C-T

21398640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738735-C-T

21398646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738729-G-A

21398655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738720-A-T

21398680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738706-A-G

21398733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738653-G-A

21398733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738653-G-T

http://identifiers.org/hco/9/GRCh38#21398757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88738629-A-C

21398795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738578-C-T

21398817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738556-G-A

21398834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738539-G-T

21398846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738527-G-A

21398846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738527-G-C

21398846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738527-G-T

http://identifiers.org/hco/9/GRCh38#21398849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88738524-C-A

21398849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738524-C-T

21398856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738517-G-T

21398863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738479-A-G

21398873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738469-G-T

21398881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738461-C-T

21398921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738421-G-T

21398944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738398-T-A

21398945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738397-G-T

21398996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738345-G-T

21399008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738333-G-C

21399019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738322-T-C

21399079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738255-G-A

http://identifiers.org/hco/9/GRCh38#21399108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88738226-C-A

21399108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88738226-C-T

21399125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88734457-A-G

http://identifiers.org/hco/9/GRCh38#21399154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88734429-C-A

21399242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88734344-T-C

21403206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88734578-A-G

21403209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88734581-G-A

21403209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88734581-G-T

http://identifiers.org/hco/9/GRCh38#21403219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88734591-C-A

21403236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88734608-C-T

http://identifiers.org/hco/9/GRCh38#21403263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88734636-C-A

21403279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88734652-G-C

21403279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88734652-G-T

21403283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88734656-A-G

21403286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88734659-A-G

http://identifiers.org/hco/9/GRCh38#21403298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88734671-C-A

21403308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: non coding transcript exon variant
orthologous variants: 88734681-A-G

http://identifiers.org/hco/9/GRCh38#21403320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88734693-A-C

21403320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: non coding transcript exon variant
orthologous variants: 88734693-A-T

http://identifiers.org/hco/9/GRCh38#21403323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88734696-C-A

21403324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: non coding transcript exon variant
orthologous variants: 88734697-G-A

21403324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: non coding transcript exon variant
orthologous variants: 88734697-G-C

21403324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: non coding transcript exon variant
orthologous variants: 88734697-G-T

21403328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: non coding transcript exon variant
orthologous variants: 88734701-C-T

21403332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: non coding transcript exon variant
orthologous variants: 88734705-C-T

21403333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: non coding transcript exon variant
orthologous variants: 88734706-G-A

21403359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: non coding transcript exon variant
orthologous variants: 88734732-C-T

http://identifiers.org/hco/9/GRCh38#21403392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88734765-C-A

http://identifiers.org/hco/9/GRCh38#21403464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88734822-C-A

21403464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: non coding transcript exon variant
orthologous variants: 88734822-C-T

21403478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88734840-T-C

21403478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88734840-T-G

http://identifiers.org/hco/9/GRCh38#21403486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88734859-C-A

21403488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88734861-A-G

21403504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88734872-G-A

http://identifiers.org/hco/9/GRCh38#21403540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88734918-C-A

21403540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88734918-C-T

21403605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88734984-G-A

21403605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88734984-G-T

http://identifiers.org/hco/9/GRCh38#21403614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88734995-C-A

21403614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88734995-C-G

21403614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88734995-C-T

21403619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88735000-T-C

21408819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88521926-T-A

21408826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88521911-T-G

21408957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88753538-G-A

21408963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88753544-A-G

21409022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88753601-G-A

21409022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88753601-G-T

21409037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88753616-G-A

21409049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88753625-G-C

21409049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88753625-G-T

21409079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88753655-T-A

21409079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88753655-T-C

21409099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88753676-G-A

21409150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753735-A-G

21409157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753742-C-T

21409165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753750-A-G

http://identifiers.org/hco/9/GRCh38#21409193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88753778-A-C

21409193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753778-A-T

21409216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753801-C-G

21409220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753805-G-A

21409220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753805-G-C

21409220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753805-G-T

21409228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753813-T-C

http://identifiers.org/hco/9/GRCh38#21409238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88753823-C-A

21409238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753823-C-G

21409241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753826-T-C

21409254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753839-G-A

21409280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753865-G-C

21409290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753875-G-A

21409313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753898-G-T

21409344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753929-A-G

http://identifiers.org/hco/9/GRCh38#21409359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88753944-C-A

21409359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753944-C-G

21409359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753944-C-T

21409362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753947-C-T

http://identifiers.org/hco/9/GRCh38#21409367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88753952-A-C

21409368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753953-G-A

http://identifiers.org/hco/9/GRCh38#21409393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88753978-A-C

21409393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88753978-A-G

21409418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754003-A-G

21409418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754003-A-T

21409435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754020-A-T

21409442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754027-A-G

21409444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754029-C-T

21409450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754035-A-G

21409458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754043-G-A

21409461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754046-C-T

21409472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754057-C-T

21409473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754058-T-G

http://identifiers.org/hco/9/GRCh38#21409497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88754082-A-C

21409497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754082-A-G

21409498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754083-T-A

21409498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754083-T-C

21409510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754095-C-T

21409539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754124-C-T

21409543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754128-G-T

21409551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754136-G-A

21409557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754142-G-A

21409557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754142-G-T

21409561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754146-G-A

http://identifiers.org/hco/9/GRCh38#21409590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88754175-C-A

21409590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754175-C-G

21409590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754175-C-T

21409623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754208-A-G

21409623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754208-A-T

http://identifiers.org/hco/9/GRCh38#21409632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88754217-A-C

21409632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754217-A-G

21409632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754217-A-T

http://identifiers.org/hco/9/GRCh38#21409653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88754238-C-A

21409653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754238-C-T

21409701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754286-C-G

21409701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754286-C-T

21409712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754297-T-G

21409713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754298-C-T

21409734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754319-G-A

21409735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754320-A-G

21409780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754367-C-G

21409808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754394-T-C

http://identifiers.org/hco/9/GRCh38#21409827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88754410-C-A

21409857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754433-G-A

21409857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754433-G-T

http://identifiers.org/hco/9/GRCh38#21409870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88754446-C-A

21409870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754446-C-G

21409870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754446-C-T

http://identifiers.org/hco/9/GRCh38#21409899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88754472-C-A

21409899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754472-C-T

http://identifiers.org/hco/9/GRCh38#21409937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88754490-C-A

21409937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754490-C-G

21410019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754576-A-G

21410019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754576-A-T

21410025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754582-T-C

21410092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754645-G-A

21410092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88754645-G-T

http://identifiers.org/hco/9/GRCh38#21410116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88754669-A-C

21414323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88525311-T-C

21414410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88525217-T-C

21417812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88617485-T-A

21417819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88617480-T-G

21418000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: non coding transcript exon variant
orthologous variants: 88617311-T-C

21419004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88616125-A-G

21419021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88616107-C-T

21419183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88615932-C-T

21419275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88615867-G-T

21419568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88615619-T-A

21419623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88615567-T-G

21419722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88615476-T-A

21419815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88615381-G-T

http://identifiers.org/hco/9/GRCh38#21420174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88760038-C-A

21420174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 88760038-C-T

21420214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88760074-C-T

http://identifiers.org/hco/9/GRCh38#21420215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88760075-C-A

http://identifiers.org/hco/9/GRCh38#21420422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88760287-C-A

21420422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88760287-C-G

21420422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88760287-C-T

21420482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88760346-T-C

http://identifiers.org/hco/9/GRCh38#21420546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88760412-C-A

21420546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88760412-C-G

http://identifiers.org/hco/9/GRCh38#21420580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88760446-C-A

21420580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88760446-C-T

http://identifiers.org/hco/9/GRCh38#21420588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88760454-C-A

21420588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88760454-C-T

21420667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88760519-G-A

21420667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88760519-G-C

21420667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88760519-G-T

http://identifiers.org/hco/9/GRCh38#21420720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88760574-C-A

21420720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88760574-C-G

http://identifiers.org/hco/9/GRCh38#21420756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88760610-C-A

21420756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88760610-C-T

http://identifiers.org/hco/9/GRCh38#21420830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88614360-A-C

21420830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88614360-A-G

21420830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88614360-A-T

21421106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88614099-T-C

21436244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88629911-C-T

21436359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88629816-T-C

21436390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88629789-G-A

21436407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88629772-T-C

21436490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88629659-G-C

http://identifiers.org/hco/9/GRCh38#21436553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88629403-C-A

21436674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88629295-A-G

21437022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88628972-A-G

21437192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88628797-G-C

21439937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88753193-C-T

http://identifiers.org/hco/9/GRCh38#21439965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88753220-C-A

21439965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88753220-C-T

21439968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88753223-G-A

21440009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88753260-A-T

21440182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88753434-A-G

21440326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88768143-T-A

21440326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88768143-T-C

21440326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88768143-T-G

http://identifiers.org/hco/9/GRCh38#21440370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88768187-C-A

21440370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88768187-C-T

http://identifiers.org/hco/9/GRCh38#21440377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88768194-C-A

http://identifiers.org/hco/9/GRCh38#21440395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88768212-C-A

21440395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88768212-C-T

21440421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88768238-G-T

21440459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768276-T-G

http://identifiers.org/hco/9/GRCh38#21440471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88768288-C-A

21440474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768291-C-T

21440484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768300-C-G

21440502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768318-T-G

21440506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768322-C-G

21440506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768322-C-T

21440507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768323-G-A

21440537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768353-C-T

21440541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768357-G-A

21440541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768357-G-C

21440559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768375-T-C

21440567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768383-C-G

21440567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768383-C-T

http://identifiers.org/hco/9/GRCh38#21440569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88768385-C-A

21440569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768385-C-T

21440578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768394-G-C

21440587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768403-C-G

21440587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768403-C-T

21440614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768430-G-A

21440616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768432-A-G

21440624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768440-G-A

21440624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768440-G-T

http://identifiers.org/hco/9/GRCh38#21440627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88768443-C-A

21440627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768443-C-T

http://identifiers.org/hco/9/GRCh38#21440628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88768444-C-A

21440630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768446-G-A

21440630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768446-G-C

21440630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768446-G-T

21440673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768489-A-G

21440676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768492-C-T

21440679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768495-G-C

21440685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768501-G-A

21440690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768506-T-A

21440693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768509-C-T

21440695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768511-A-G

21440695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768511-A-T

21440699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768515-G-A

21440721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768537-C-T

21440726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768542-G-A

21440734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768550-C-G

21440734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768550-C-T

21440775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768591-C-T

21440791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768607-A-G

21440791-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768607-A-T

21440792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768608-T-C

21440808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768624-G-A

21440811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768627-G-A

http://identifiers.org/hco/9/GRCh38#21440841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88768657-C-A

21440841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768657-C-T

http://identifiers.org/hco/9/GRCh38#21440846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88768662-C-A

21440851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768667-A-G

21440888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768704-G-A

21440888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768704-G-C

21440888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768704-G-T

21440890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768706-G-A

21440890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768706-G-T

21440902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768718-C-T

http://identifiers.org/hco/9/GRCh38#21440904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88768720-C-A

21440904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768720-C-T

21440915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768731-T-C

21440915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768731-T-G

21440921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768737-C-T

21440931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768747-G-C

21440931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768747-G-T

21440934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768750-G-A

21440959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768775-C-G

21440963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768779-C-G

21440963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768779-C-T

21440965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768781-A-G

21441047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768863-C-T

21441055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768871-A-G

21441065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768881-G-A

21441068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768884-G-T

21441117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768933-C-T

21441122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768938-G-C

21441124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768940-T-C

21441128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768944-G-A

21441128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768944-G-T

21441134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768951-A-G

21441144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768960-T-C

http://identifiers.org/hco/9/GRCh38#21441145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88768961-C-A

http://identifiers.org/hco/9/GRCh38#21441162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88768977-C-A

21441162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88768977-C-T

http://identifiers.org/hco/9/GRCh38#21441261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88769079-C-A

21441261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88769079-C-G

21441261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88769079-C-T

http://identifiers.org/hco/9/GRCh38#21441275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88769093-C-A

21441275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88769093-C-T

21444135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88624592-T-C

21444161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88624560-T-G

http://identifiers.org/hco/9/GRCh38#21444252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88624481-A-C

21444366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88624361-T-C

21444457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88624273-A-T

21444656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88624089-C-T

http://identifiers.org/hco/9/GRCh38#21448248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88661528-C-A

21448248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88661528-C-G

21448593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88661837-A-G

21448736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88661991-T-A

21448737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88661992-G-A

21453062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88783221-G-A

21453289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88783436-C-T

http://identifiers.org/hco/9/GRCh38#21453414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88783598-A-C

21453414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88783598-A-G

21453434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88783639-T-C

21453560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88783790-G-C

21453664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88783910-A-G

21453919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88784261-C-T

21454237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88784666-T-C

21454239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88784668-C-T

21454378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88784770-T-C

21454504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88784873-G-T

http://identifiers.org/hco/9/GRCh38#21454517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88784882-C-A

21454517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88784882-C-G

http://identifiers.org/hco/9/GRCh38#21455268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88785489-A-C

21455268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88785489-A-G

21455313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88785532-T-C

21455402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88785695-A-T

21455431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88785724-A-T

21455453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88785749-T-C

21455567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88785849-G-T

21455587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88785865-G-A

21455587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88785865-G-T

http://identifiers.org/hco/9/GRCh38#21455591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88785869-C-A

21455591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88785869-C-T

21455631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88785906-T-A

21455631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88785906-T-C

21455686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88785957-T-C

http://identifiers.org/hco/9/GRCh38#21455755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88614653-C-A

21455755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88614653-C-T

21455763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88614645-G-T

http://identifiers.org/hco/9/GRCh38#21455778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88614631-A-C

21455778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88614631-A-G

21455788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88614621-A-G

http://identifiers.org/hco/9/GRCh38#21455808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88614602-C-A

21455808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88614602-C-G

21455808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88614602-C-T

21455855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88614556-A-G

21455857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88614554-G-T

http://identifiers.org/hco/9/GRCh38#21455928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88614506-C-A

21455928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88614506-C-T

21455964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88614468-G-A

21455964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88614468-G-C

21455964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88614468-G-T

21456019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88614416-G-A

21456019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88614416-G-T

http://identifiers.org/hco/9/GRCh38#21456079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88614360-A-C

21456079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88614360-A-G

21456249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88614211-A-G

21456340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88614116-C-T

http://identifiers.org/hco/9/GRCh38#21456347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88614109-A-C

21456549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88766903-G-C

21456552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88766906-G-C

21456569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88766923-T-C

21456670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88767019-A-G

21468812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88793075-C-T

21468876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88793165-T-C

21468982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88793307-G-C

21469206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88793484-G-A

21470723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88795317-A-G

21470792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88795376-T-C

21470893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88795480-A-G

21470970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88795545-G-A

21470995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88795559-C-T

21473380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88745996-T-G

21473406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88745970-T-C

21473417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88745959-G-C

21473458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88745918-G-C

21473458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88745918-G-T

21473535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88745843-G-A

http://identifiers.org/hco/9/GRCh38#21473597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88745773-C-A

21473598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88745772-A-G

21473604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88745766-T-C

21473650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88745714-G-A

21473652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88745712-G-A

21473652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88745712-G-C

http://identifiers.org/hco/9/GRCh38#21478712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88795939-A-C

http://identifiers.org/hco/9/GRCh38#21478715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88795942-A-C

21478715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88795942-A-G

21479071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796283-G-A

21479098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796310-T-C

21479111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796323-C-T

21479163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796382-A-G

21479163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796382-A-T

21479220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796442-T-C

21479480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796673-C-T

http://identifiers.org/hco/9/GRCh38#21479489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88796682-C-A

21479528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796720-G-A

21479580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796758-G-A

21479933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88797128-G-A

21479933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88797128-G-T

21479960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88797149-T-A

21480555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88797372-C-G

21480571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88797388-C-T

21480736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88797492-T-A

21480736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88797492-T-C

21480789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88797534-T-A

21480840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88797582-T-A

21480855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88797597-T-C

21481089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88797813-T-C

21481104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88797827-C-T

21481171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88797896-C-G

21481171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88797896-C-T

21481176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88797901-G-A

21481205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88797930-C-T

http://identifiers.org/hco/9/GRCh38#21481206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88797931-A-C

21481242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88797967-G-A

21481290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798015-C-G

21481297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798022-C-G

21481334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798059-C-T

http://identifiers.org/hco/9/GRCh38#21481421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88798146-A-C

21481454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798179-G-C

21481454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798179-G-T

21481507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798232-G-A

21481507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798232-G-T

21481518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798243-G-A

21481644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798366-G-A

21481644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798366-G-C

21481669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798391-G-T

21481674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798396-A-G

http://identifiers.org/hco/9/GRCh38#21481783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88798498-A-C

21481783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798498-A-G

http://identifiers.org/hco/9/GRCh38#21481834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88798550-C-A

21481834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798550-C-G

21481850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798566-A-G

21481867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798583-T-C

21481867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798583-T-G

21481916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798630-T-C

21481956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798671-C-T

21482206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798922-A-G

http://identifiers.org/hco/9/GRCh38#21482238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#88798954-C-A

21482238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88798954-C-T

21482320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88799033-G-T

21482347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88799063-G-T

21482631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88799328-A-G

21482681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88799380-T-C

21482901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88799967-C-T

http://identifiers.org/hco/9/GRCh38#21482929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88799992-C-A

21482929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88799992-C-G

21482929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88799992-C-T

21483049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88800119-T-C

21492060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88805781-C-G

21492068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88805789-T-C

21492075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88805796-C-T

21492235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88805929-C-T

21492316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88806001-G-A

21492348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88806034-G-A

21492596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88806283-G-A

21492796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88806456-G-T

http://identifiers.org/hco/9/GRCh38#21492798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88806458-A-C

21492798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88806458-A-G

21492827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88806484-G-A

21492835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88806491-G-A

21493260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88806604-T-C

21493401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88806740-A-G

21493433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88806771-T-G

http://identifiers.org/hco/9/GRCh38#21493513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88806853-A-C

21493514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88806854-G-A

21493567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88806893-C-T

21493648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88806971-T-C

21493827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88807142-T-C

21493941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88807235-C-T

21495464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88807797-T-A

21495464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88807797-T-C

21495475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88807808-A-T

21495575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88807894-A-G

21495579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88807898-G-A

21496776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88808369-T-C

21497176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88808752-G-A

21497476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88809020-T-C

21497594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88809168-G-C

21497691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88809270-A-G

21498079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88809594-G-A

21498144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88809647-A-G