63423647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 9041631-G-A

63423647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 9041631-G-T

http://identifiers.org/hco/3/GRCh38#63424529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9032368-C-A

63424547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9032355-A-G

63424754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9032143-T-C

63424756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9032141-G-A

63424790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9032112-G-C

63424870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9032009-G-A

63425059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9031857-T-C

63425077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9031846-C-G

63425077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9031846-C-T

63426942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9030655-A-T

63427130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9030485-G-C

63427130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9030485-G-T

http://identifiers.org/hco/3/GRCh38#63427249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9030376-C-A

63427264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9030361-T-A

http://identifiers.org/hco/3/GRCh38#63427332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9030296-C-A

63427332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9030296-C-T

http://identifiers.org/hco/3/GRCh38#63427515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9030137-C-A

http://identifiers.org/hco/3/GRCh38#63427584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9030079-C-A

http://identifiers.org/hco/3/GRCh38#63427597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9030066-A-C

63427601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9030062-T-A

63427635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9030029-C-T

63427663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9030013-G-A

63427663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9030013-G-T

63427716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9029961-G-C

63428545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9029100-C-G

63429821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9027689-G-A

63429831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9027679-G-A

63429831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9027679-G-C

63429831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9027679-G-T

63429865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9027647-C-G

63429865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9027647-C-T

63429977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9027536-G-A

63430365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9027186-C-T

63430522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -G-A

http://identifiers.org/hco/3/GRCh38#63430572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -A-C

63430924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -G-A

63430993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9025521-G-C

63431154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9025383-C-T

63431195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9025350-C-T

63431208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9025337-T-C

63431296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9025251-A-G

63431396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9025154-G-A

63431466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9025086-G-A

63431592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9024869-T-C

63431756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9024616-A-G

63431756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9024616-A-T

http://identifiers.org/hco/3/GRCh38#63431815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9024559-A-C

63431815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9024559-A-T

http://identifiers.org/hco/3/GRCh38#63431869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9024482-A-C

63431869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9024482-A-T

63431871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9024480-C-G

63431871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9024480-C-T

http://identifiers.org/hco/3/GRCh38#63431984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9024362-A-C

63432102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9024285-T-A

63432116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9024271-C-T

63432370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9024053-G-A

63432370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9024053-G-T

63432385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9024039-A-G

63432832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9023000-C-G

63433103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9022808-G-A

63433103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9022808-G-C

63433515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9022394-T-C

63433569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9022350-A-G

63433638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9022300-G-A

63433717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9022258-T-A

63433718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9022257-G-A

63433718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9022257-G-T

http://identifiers.org/hco/3/GRCh38#63434122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9021873-A-C

63435052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9021340-A-G

63435102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9021268-C-T

63435516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9020915-G-A

63438537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9020814-T-C

63438768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9020403-G-A

63439208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9019978-A-G

63439283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9019906-T-A

63439283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9019906-T-C

63439442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9019755-G-A

63439457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9019740-C-T

63439905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9019268-C-G

63440072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9018687-G-C

63440245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9018493-T-C

63440480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9018252-G-C

63440714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9018033-C-G

63441071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9017783-G-A

63441570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9017321-T-C

63441651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9017271-G-A

63441651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9017271-G-T

63441689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9017234-G-A

63441689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9017234-G-C

63441692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9017231-G-T

63441738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9017136-G-A

63441819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9016970-G-A

63441870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9016931-A-G

http://identifiers.org/hco/3/GRCh38#63441925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9016882-A-C

63441925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9016882-A-G

63442049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9016745-T-A

63442370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9016470-A-T

63442497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9016345-G-A

63442584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9016261-C-T

63442719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9016146-G-A

http://identifiers.org/hco/3/GRCh38#63442929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9015938-C-A

63442929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9015938-C-T

63442974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9015895-A-G

http://identifiers.org/hco/3/GRCh38#63443034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9015838-A-C

63443110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 9015763-A-G

63443160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 9015713-G-A

63443295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9015581-C-T

63443487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9015393-T-C

63443504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9015266-G-A

63443506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9015264-G-A

63443506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9015264-G-T

63443508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9015262-G-A

63443508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9015262-G-T

63443528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9015242-G-A

63443530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9015240-G-T

63443586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9015125-T-C

http://identifiers.org/hco/3/GRCh38#63443587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9015124-C-A

63443587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9015124-C-G

63443588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9015123-T-C

63443588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9015123-T-G

63444058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9014658-T-C

63444234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9014489-G-A

63444777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9013956-G-C

63444832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9013909-C-G

63444832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9013909-C-T

63445024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9013750-C-T

63445170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9013616-A-G

63445450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9013352-T-A

http://identifiers.org/hco/3/GRCh38#63445473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9013329-C-A

63445535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9013266-T-A

63445551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9013250-A-T

http://identifiers.org/hco/3/GRCh38#63445703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9013130-C-A

63445703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9013130-C-T

63445817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9013031-A-G

63446012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9012845-G-A

63446616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9012292-A-G

63446731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9012169-G-T

63446886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9012039-T-C

63447037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9011907-C-T

63447132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9011811-G-C

63447507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9011459-A-G

63447555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9011413-T-C

63447593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9011381-T-C

63447593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9011381-T-G

63447677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9011288-A-T

63447691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9011274-G-A

63448612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9011053-C-T

63448669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9010995-T-A

http://identifiers.org/hco/3/GRCh38#63448746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9010928-A-C

63448746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9010928-A-G

63448868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9010809-T-A

63448902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9010775-G-A

63449037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9010650-A-T

63449097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9010592-T-C

63449128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9010563-A-G

63449164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9010530-G-A

63449325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9010393-C-T

63449376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9010342-G-T

63449387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9010331-C-T

63449428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9010292-T-G

63450155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9009569-A-G

63450168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9009556-G-C

63450172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9009552-C-T

63450206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9009529-T-G

63450298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9009465-T-C

63450453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9009330-T-C

63450548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9009230-G-A

63450562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9008620-T-C

http://identifiers.org/hco/3/GRCh38#63450567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9008615-A-C

63450601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9008588-T-A

63450711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9008475-C-T

63450750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9008439-G-A

63450849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9008361-G-A

63450888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9008321-C-T

http://identifiers.org/hco/3/GRCh38#63451071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9008162-C-A

63451071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9008162-C-T

63451152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9008102-G-A

63451152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9008102-G-T

63451180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9008090-T-C

http://identifiers.org/hco/3/GRCh38#63451257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9008037-A-C

63451338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9007956-T-C

63451467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9007826-C-G

63451631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9007684-C-T

63451688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9007626-G-A

63451727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9007599-A-G

63451787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9007552-T-A

http://identifiers.org/hco/3/GRCh38#63451929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9007405-C-A

http://identifiers.org/hco/3/GRCh38#63452015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9007329-C-A

63452015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9007329-C-G

63452015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9007329-C-T

63452017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9007327-G-A

63452017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9007327-G-T

http://identifiers.org/hco/3/GRCh38#63452051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9007290-C-A

63452069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 9007272-A-G

63452093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9007251-T-C

63452184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9007162-T-C

http://identifiers.org/hco/3/GRCh38#63452207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9007147-C-A

63452207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9007147-C-T

63452228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9007118-G-A

63452228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9007118-G-C

63452228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9007118-G-T

63452230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9007116-A-G

63452270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9007073-T-C

63452305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9007035-A-G

63452451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9006895-G-T

63452561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9006788-G-A

63452561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9006788-G-C

63452762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9006621-G-A

http://identifiers.org/hco/3/GRCh38#63452860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#9006533-A-C

63452899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9006496-A-G

63452905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9006490-G-A

63452911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9006484-A-G

63453205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9004931-C-G

63453447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9004697-C-T

63453533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9004611-G-A

63453752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9003889-G-A

63453978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9003679-T-G

63454104-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9003560-A-T

63454729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9002651-G-C

63454810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9002584-G-A

63455322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9001974-G-C

63455380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9001939-C-T

63455414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9001905-G-A

63455414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9001905-G-T

63455619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9001720-G-A

63456371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9000748-T-C

63456510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9000606-T-C

63456741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9000413-C-T

63456906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9000286-C-G

63456979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9000223-T-A

63456979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9000223-T-C

63457041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9000160-G-A

63457369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8999994-T-A

63457369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8999994-T-C

63457433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8999947-G-T

63457904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8996018-A-G

63457914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8996008-C-T

63458498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8995451-G-A

63458767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8995217-G-A

63459069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8994945-G-A

63459201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8994803-A-G

63459255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8994740-T-C

63459275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8994720-C-G

63459307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8994688-T-G

http://identifiers.org/hco/3/GRCh38#63459423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8994577-C-A

63459423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8994577-C-T

63459469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8994532-T-C

63459904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8994116-T-C

http://identifiers.org/hco/3/GRCh38#63459982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8994049-A-C

63460020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8994019-C-T

63460088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8993954-T-C

63460097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8993945-G-C

63460188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8993872-C-G

http://identifiers.org/hco/3/GRCh38#63460321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8993750-C-A

63460321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8993750-C-G

63460371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8993700-C-T

63460671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8992500-G-C

http://identifiers.org/hco/3/GRCh38#63460690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8992481-C-A

63460690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8992481-C-T

63460765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8992426-A-T

63460781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8992409-C-T

63460868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8992345-G-C

63460868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8992345-G-T

63460890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8992325-G-A

63461016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8992227-G-A

63461055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8992201-C-T

http://identifiers.org/hco/3/GRCh38#63461456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8991802-C-A

63461456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8991802-C-T

63461624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8991629-C-T

63461706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8991544-A-G

63461975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8991305-T-C

63462205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8991105-C-T

63462233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8991077-C-T

http://identifiers.org/hco/3/GRCh38#63462375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8990858-C-A

63462539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8990756-T-C

63462573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8990722-G-A

63462795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8990511-T-C

63467280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8985855-T-C

63467281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8985854-A-G

63467342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8985803-T-G

63467384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8985770-T-A

63467541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8985624-G-A

63467547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8985618-C-T

63467650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8985542-T-C

63468291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8984945-G-A

63468418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8984805-C-T

http://identifiers.org/hco/3/GRCh38#63468447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8984774-C-A

63468447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8984774-C-T

63468964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8984584-G-T

63470392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8982695-C-T

63470463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8982629-A-G

63470585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8982526-C-T

63470845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8982470-C-T

63470948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8982366-C-T

63471200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8982152-A-G

63471217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8982133-C-T

63471279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8982015-A-G

63471566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8981465-T-C

http://identifiers.org/hco/3/GRCh38#63471614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8981432-C-A

http://identifiers.org/hco/3/GRCh38#63471615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8981431-A-C

63471647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8981394-G-A

63471705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8981326-T-A

63471821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8981226-G-A

63472298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8980799-G-A

63472298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8980799-G-T

63472506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8980576-A-G

63472708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8980199-A-G

63472722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8980185-G-A

63472945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8979981-T-C

63473049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8979884-C-T

http://identifiers.org/hco/3/GRCh38#63474581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8979701-A-C

63474588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8979674-G-A

63474595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8979667-T-A

63474595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8979667-T-G

63474598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8979664-T-A

63474598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8979664-T-G

http://identifiers.org/hco/3/GRCh38#63474610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8979652-A-C

63474610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8979652-A-G

http://identifiers.org/hco/3/GRCh38#63474615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8979647-C-A

63474615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8979647-C-G

63474615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8979647-C-T

63474883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8979419-G-A

http://identifiers.org/hco/3/GRCh38#63475102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8979150-A-C

63475114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8979138-G-C

63476967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8978918-G-A

63477140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8978779-G-A

63477220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8978702-C-T

63477308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8978628-C-T

63478019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8978486-G-A

63478062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8978445-G-T

63478080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8978427-T-C

63478137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8978374-A-G

63478266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8978244-C-T

63478375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8978133-T-C

63478385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8978122-T-G

63478427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8978082-A-G

63478690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8977987-T-C

63478888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8977872-T-A

63478888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8977872-T-C

63478889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8977871-G-A

63478930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8977830-C-G

63479197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8977599-T-A

63479236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8977560-C-T

63479288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8977507-T-C

63479306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8977489-A-G

63479489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8977332-G-C

http://identifiers.org/hco/3/GRCh38#63479508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8977313-C-A

63479685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8977160-C-T

63480178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8976866-C-G

63480287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8976752-G-A

http://identifiers.org/hco/3/GRCh38#63480290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8976749-C-A

63480290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8976749-C-G

63480450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8976585-G-A

http://identifiers.org/hco/3/GRCh38#63480563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8976508-C-A

63480564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8976507-T-C

http://identifiers.org/hco/3/GRCh38#63480616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8976474-C-A

63480652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8976438-C-T

http://identifiers.org/hco/3/GRCh38#63480683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8976404-C-A

63480683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8976404-C-T

http://identifiers.org/hco/3/GRCh38#63480746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8976341-C-A

63480746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8976341-C-G

63480746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8976341-C-T

http://identifiers.org/hco/3/GRCh38#63480906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8976179-C-A

63480906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8976179-C-T

63480945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8976140-C-T

63480967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8976118-G-A

63480973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8976112-C-T

http://identifiers.org/hco/3/GRCh38#63481081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8976020-C-A

63481081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8976020-C-T

http://identifiers.org/hco/3/GRCh38#63481175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8975931-C-A

63481175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8975931-C-T

63484151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8975012-A-G

http://identifiers.org/hco/3/GRCh38#63484276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8974882-A-C

63484383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8974772-T-C

63484455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8974702-T-C

http://identifiers.org/hco/3/GRCh38#63487764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8973511-C-A

63487840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8973432-G-A

http://identifiers.org/hco/3/GRCh38#63487938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8973324-C-A

63488047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8973222-C-T

63488116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8973148-G-C

63491941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8971049-G-A

63491941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8971049-G-T

63491989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8970991-G-A

63492201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8970823-T-A

63492201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8970823-T-C

63492584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8970490-G-A

63492815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8969855-G-A

63492867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8969806-T-C

63492892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8969789-C-T

http://identifiers.org/hco/3/GRCh38#63493092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8969594-C-A

http://identifiers.org/hco/3/GRCh38#63493148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8969559-C-A

63493389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8969368-A-T

63493476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8969292-G-A

63493529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8969248-T-C

63493978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8969095-G-C

63493978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8969095-G-T

63493983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8969090-T-C

63493983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8969090-T-G

63494004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8969072-T-C

63494010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8969067-G-C

http://identifiers.org/hco/3/GRCh38#63494115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8968980-C-A

63494174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8968920-T-C

63494257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8968827-G-C

63494272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8968809-C-T

63494357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8968741-G-A

63494385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8968717-G-C

63494385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8968717-G-T

63494387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8968715-T-G

63494438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8968671-T-A

63494438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8968671-T-C

63494447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8968662-A-G

63494758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8968264-G-A

63494911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8968115-T-C

http://identifiers.org/hco/3/GRCh38#63494961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8968070-A-C

63495098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8967934-C-T

63495299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8967747-C-T

http://identifiers.org/hco/3/GRCh38#63496333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8966421-C-A

63496393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8966373-C-T

63496401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8966362-A-T

63496490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8966271-T-C

http://identifiers.org/hco/3/GRCh38#63496999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8965470-A-C

63496999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8965470-A-G

63497088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8965381-T-C

63497280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8965191-A-G

63497287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8965184-C-T

63497309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8965168-A-G

63497342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8965152-T-C

63497822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8964709-A-G

63497940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8964595-G-A

63497981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8964554-A-G

63498055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8964481-G-C

63498129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8964408-G-A

63498343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8964202-C-T

63498388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8964160-G-A

63498588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8963969-G-A

63498689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8963883-G-A

63498732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8963838-G-A

63498779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8963793-G-A

63499114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8963671-T-C

63499152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8963635-G-C

63499233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8963559-G-A

63499376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8963415-A-G

63499392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8963391-T-C

63499394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8963388-G-A

63499428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8963358-T-C

63499697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8963154-C-T

http://identifiers.org/hco/3/GRCh38#63499860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8963030-C-A

63499990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8962919-T-A

http://identifiers.org/hco/3/GRCh38#63502856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8962665-C-A

63502888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8962646-A-G

63503069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8962452-C-G

63503101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8962421-C-T

63503124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8962401-G-A

63503124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8962401-G-C

63503164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8962353-C-T

63503308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8962208-T-G

63503310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8962206-T-C

http://identifiers.org/hco/3/GRCh38#63503481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8962052-A-C

63503513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8962021-T-C

63503546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8961988-T-C

63503734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8961816-A-G

63503914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8961648-T-C

63503955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8961606-A-G

63504029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8961536-C-T

63504219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8961051-T-C

63506109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8960869-G-C

63506109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8960869-G-T

63506123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8960854-C-T

63506253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8960772-T-C

63508659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8959516-G-C

63508787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8959371-A-G

http://identifiers.org/hco/3/GRCh38#63508797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8959361-C-A

63509004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8959162-A-G

63509533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8958907-T-C

http://identifiers.org/hco/3/GRCh38#63509821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8958526-A-C

63510036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8958283-C-T

63510084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8958223-G-A

63510208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8958106-T-C

http://identifiers.org/hco/3/GRCh38#63510235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8958079-C-A

63510235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8958079-C-T

63510237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8958077-G-A

http://identifiers.org/hco/3/GRCh38#63510258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8958038-C-A

63510333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8957833-T-G

63510344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8957822-C-T

63510414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8957757-C-T

63510427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8957744-G-T

63510558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8957623-A-T

63510696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8957009-T-C

63510905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8956804-A-G

63510937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8956772-G-A

63510937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8956772-G-C

http://identifiers.org/hco/3/GRCh38#63510942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8956767-C-A

63510942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8956767-C-T

63510965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8956747-G-T

63510979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8956736-G-A

63510979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8956736-G-T

63511090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8956554-T-C

63511103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8956539-T-A

http://identifiers.org/hco/3/GRCh38#63511319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8956334-C-A

63511319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8956334-C-T

63511335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8956318-A-G

63511373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8956277-T-C

63511377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8956273-G-A

63511462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8956193-C-G

63511503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8956153-C-T

63511506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8956150-A-G

63511535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8956128-C-T

63511619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8956070-G-A

63511694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8955933-G-C

63511769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8955859-A-G

63511797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8955831-G-A

63511932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8955716-T-C

http://identifiers.org/hco/3/GRCh38#63512095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8955581-C-A

63512195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8955489-C-T

http://identifiers.org/hco/3/GRCh38#63512708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8955008-C-A

63512720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8954996-T-A

63513747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8954202-G-A

63514037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8953920-T-C

63514375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8950894-C-G

63514405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8950864-A-G

63514426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8950846-C-G

63514576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8950676-T-C

63514613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8950664-T-G

63514794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8950484-G-A

63514911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8950427-T-C

63514936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8950401-C-T

63514947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8950390-T-C

63514966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8950372-T-C

63514982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8950356-T-C

63515023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8950314-G-C

63515268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8950082-C-G

63515338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8950014-T-C

63515649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8949713-A-G

63516046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8949472-A-T

63516117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8949413-A-G

63516198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8949371-T-G

63516239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8949331-T-C

63516377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8949198-A-G

63516564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8949013-T-G

63516695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8948908-T-G

63516740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8948858-G-A

63516740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8948858-G-C

63516742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8948856-A-G

63516802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8948789-A-G

63516856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8948735-G-A

63517148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8948147-G-A

63517148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8948147-G-T

http://identifiers.org/hco/3/GRCh38#63517239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8948070-C-A

63517311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8947994-G-A

63517319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8947986-A-T

63517385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8947916-T-C

63519715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8944664-C-T

63519797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8944595-G-A

63519797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8944595-G-T

63521650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8941699-A-G

63521700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8941652-G-C

http://identifiers.org/hco/3/GRCh38#63521907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8941438-A-C

63521920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8941425-G-A

63526316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8940876-C-T

http://identifiers.org/hco/3/GRCh38#63526511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8940720-A-C

63526580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8940657-C-T

63527179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8940401-G-C

63527184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8940396-A-G

63527218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8940370-C-T

63527293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8940300-T-G

63527601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8940009-A-G

63527633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8939988-C-T

63527634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8939987-T-C

63527672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8939958-G-C

63527678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8939955-C-T

63527700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8939933-C-G

63527734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8939909-C-T

63527787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8939860-T-C

63527804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8939840-A-G

63528081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8939574-T-C

63528312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8939375-A-T

63528349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8939352-G-A

63528634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8939094-T-G

63528837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8938925-T-C

63528924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8938839-T-A

63529090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8938672-G-A

63529090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8938672-G-T

63531017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8938451-G-A

63531228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8938239-C-G

63531244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8938223-A-T

63531246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8938221-A-G

63531270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8938197-A-T

63532271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8931021-A-G

63532327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8930964-T-C

63532420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8930871-C-T

63532533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8930771-T-C

63532541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8930763-C-T

63532560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8930744-C-G

63532597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8930712-G-T

63532752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8929741-T-C

63532776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8929717-C-T

63533028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8929487-C-T

63533029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8929486-A-G

63533029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8929486-A-T

63533030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8929485-C-T

63533037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8929478-T-C

63533211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8929308-G-A

63533270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8929249-C-G

63533342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8929177-G-A

63533384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8929135-G-A

63533412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8929113-A-G

63533589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8928942-T-C

63533681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8928849-T-G

63535314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8928343-T-A

63535314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8928343-T-C

63535436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8928224-A-G

63535504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8928141-G-C

63535590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8928066-C-T

63535609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8928047-A-G

http://identifiers.org/hco/3/GRCh38#63535731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8927913-C-A

http://identifiers.org/hco/3/GRCh38#63535914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8927736-C-A

63536021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8927678-T-A

63536132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8927583-T-A

63536472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8927277-G-A

63537521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8927042-T-C

63537542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8927025-T-C

63537553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8927014-G-C

63537580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8926985-T-C

63537649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8926936-C-T

63537775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8926840-T-C

63537992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8926630-A-G

63537999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8926623-A-G

63538143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8926478-C-T

63538660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8926178-A-G

63538742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8926099-C-T

63538812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8926033-G-T

63538922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8925928-A-G

http://identifiers.org/hco/3/GRCh38#63538956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8925880-C-A

63539336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8925527-C-T

63539359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8925504-G-C

63541489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8922017-C-T

63541527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8921971-G-A

63541561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8921937-G-A

63541599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8921899-G-A

63541623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8921874-C-T

63541954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8921537-T-A

63542201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8921312-A-T

63542286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8921226-G-C

63542308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8921203-G-A

63542408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8921127-G-A

63542493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8921040-G-A

63542826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8920750-A-G

http://identifiers.org/hco/3/GRCh38#63542936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8920672-C-A

63542964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8920645-C-G

63542976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8920633-T-G

63543092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8920531-C-T

http://identifiers.org/hco/3/GRCh38#63543153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8920467-A-C

63543158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8920462-A-G

http://identifiers.org/hco/3/GRCh38#63543226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8920393-C-A

63543237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8920382-C-T

63543276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8920360-A-T

63543418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8920226-G-C

63543523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8920086-T-C

63543527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8920082-T-C

63543577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8920044-T-C

63543664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8919956-C-T

63543713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8919910-T-C

http://identifiers.org/hco/3/GRCh38#63545013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8917346-C-A

63545022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8917337-T-A

63545026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8917333-G-A

63545303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8917074-G-T

63545864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8916305-T-G

http://identifiers.org/hco/3/GRCh38#63545953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8916206-C-A

63545953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8916206-C-G

63545953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8916206-C-T

63546047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8916113-T-C

63546520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8915634-C-T

63546574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8915586-C-T

63546893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8915363-G-A

http://identifiers.org/hco/3/GRCh38#63546900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8915356-A-C

63546966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8915290-A-T

63547108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8915162-G-T

63547384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8914901-G-A

63547430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8914867-T-C

63547467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8914831-A-G

63547580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8914753-A-G

63547812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8914723-A-G

63547855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8914676-A-T

63547916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8914621-G-C

63548028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8914524-T-A

63548071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8914480-T-C

63548363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8914211-C-T

63548598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8913990-A-G

63548665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8913948-A-T

http://identifiers.org/hco/3/GRCh38#63548838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8913791-A-C

http://identifiers.org/hco/3/GRCh38#63549041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#8913610-C-A

63549129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8913561-G-T

63549202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8913490-G-A

63549911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8912513-T-G