84382660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88971721-G-A

84382856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88971521-G-A

84383006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88971393-C-T

84383384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88971036-C-T

84383444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88970991-A-T

84383500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88970951-G-A

84383616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88970833-A-T

http://identifiers.org/hco/5/GRCh38#84383814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88970641-C-A

84383817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88970619-A-G

http://identifiers.org/hco/5/GRCh38#84383872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88970567-C-A

84383920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88970518-C-T

84383942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88970493-G-C

http://identifiers.org/hco/5/GRCh38#84383943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88970492-C-A

84383943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88970492-C-G

84383943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88970492-C-T

84383989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88970446-G-T

http://identifiers.org/hco/5/GRCh38#84384162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#88970302-C-A

84384162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88970302-C-G

84384162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88970302-C-T

84384173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88970291-A-G

84384173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88970291-A-T

84384181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88970283-T-C

84384212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88970261-G-A

84384270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88970203-C-G

84384270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88970203-C-T

84384569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88969895-T-C

84384569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88969895-T-G

84384576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88969888-T-A

84384576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88969888-T-G

http://identifiers.org/hco/5/GRCh38#84384585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#88969879-C-A

84384585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88969879-C-T

84384683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88969797-G-A

84384683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88969797-G-C

84384774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88969712-G-A

84384774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88969712-G-T

http://identifiers.org/hco/5/GRCh38#84384915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#88969574-C-A

http://identifiers.org/hco/5/GRCh38#84384930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88969558-C-A

84384960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88969528-G-C

84384972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88969505-T-C

84384994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88969483-T-C

84385031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88969446-T-A

84385081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88969362-C-T

84385414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88969065-G-T

84385415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88969064-A-G

84385553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 88968934-T-C

84385557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 88968930-G-C

84385557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 88968930-G-T

84385568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88968926-G-C

84385568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88968926-G-T

84385682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88968817-G-A

84385697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88968802-C-G

84385748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 88968751-T-C

84385879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88968508-G-T

84385921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88968449-T-C

84385931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88968441-G-T

84386043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88968261-G-A

84386070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88968226-T-C

84386436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88967878-G-A

84386464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88967856-T-A

84386479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88967841-T-C

84386480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88967840-G-A

84386713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88967626-C-T

84386975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88967349-C-T

84386997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88967327-T-G

84387109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88967243-C-T

84387135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88967199-A-T

84387461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88966895-G-T

84387708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88966631-T-C

84387728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88966611-G-A

84387728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88966611-G-T

84388711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88964309-A-T

84388866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88964157-C-T

84388876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88964147-A-G

84389078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88963929-C-G

84389078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88963929-C-T

84389231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88963777-T-G

84389535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88963531-C-G

84389976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88963354-A-G

http://identifiers.org/hco/5/GRCh38#84389998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88963336-A-C

84390197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88963141-A-G

84390197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88963141-A-T

84390415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88962937-C-T

84390495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88962861-G-T

84390614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88962725-C-T

84390765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88962593-G-C

84391081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88962205-A-T

http://identifiers.org/hco/5/GRCh38#84391116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88962172-C-A

84391383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88961927-C-T

84391672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88961648-A-G

84392403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88960221-T-C

http://identifiers.org/hco/5/GRCh38#84392423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88960201-C-A

84392492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88960140-G-C

84392502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88960130-G-A

84392817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88959630-A-G

84392867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88959581-T-A

84393114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88959352-A-G

84393173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88959247-A-G

84393174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88959246-T-A

84393188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88959225-G-A

84393188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88959225-G-C

84393737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88958696-G-T

84393753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88958680-C-T

84393979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88958584-C-G

84394001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88958563-T-C

84394652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88958253-C-T

84394884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88958023-T-C

84395054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88957851-G-C

84395157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88957745-G-A

84395182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88957720-T-G

84395338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88957564-T-A

84395792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88956765-A-G

84395792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88956765-A-T

84400468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88950806-T-A

84400479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88950795-T-C

http://identifiers.org/hco/5/GRCh38#84400512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88950766-C-A

84400515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88950763-G-A

84400517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88950761-A-G

http://identifiers.org/hco/5/GRCh38#84400662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88950629-C-A

84400662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88950629-C-T

http://identifiers.org/hco/5/GRCh38#84400837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88950402-C-A

http://identifiers.org/hco/5/GRCh38#84400859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88950374-C-A

84400859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88950374-C-T

84400863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88950370-T-C

84400867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88950364-T-C

84400989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88950212-T-C

84401346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88949874-G-A

http://identifiers.org/hco/5/GRCh38#84401386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88949834-A-C

84401386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88949834-A-G

84401414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88949810-T-C

84401682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88949615-G-T

84401774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88949545-G-A

84401868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88949467-T-C

84401919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88949420-A-G

84401954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88949408-G-C

84401986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88949382-T-A

84402022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88949347-G-A

84402056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88949314-G-A

84402111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88949267-A-T

84402112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88949266-G-A

84402136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88949242-A-G

84402285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88949099-A-G

84402319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88949063-A-G

84403961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88947526-T-C

84404079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88947407-C-G

84404079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88947407-C-T

84404677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88946917-C-T

84404706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88946897-G-A

84404752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88946880-A-G

http://identifiers.org/hco/5/GRCh38#84404766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88946866-C-A

84404987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88946728-T-C

84405000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88946707-C-T

84405197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88946525-A-G

84405503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88946252-T-C

84405565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88946220-C-T

84405605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88946180-G-C

84405715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88946066-T-C

84405822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88945972-A-G

http://identifiers.org/hco/5/GRCh38#84405996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88945802-C-A

84406234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88945636-T-C

84406916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88945090-A-G

84406941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88945068-T-C

84407007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88945021-T-C

84407168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88944883-A-G

84407220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88944833-T-A

84407289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88944767-A-T

84407643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88944447-A-G

84408226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88943870-A-G

84408339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88943757-T-C

84408365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88943729-T-G

84408494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88943624-T-C

84408504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88943614-T-C

84408515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88943603-T-G

http://identifiers.org/hco/5/GRCh38#84408863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88943258-C-A

84408970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88943147-A-G

84409021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88943091-T-A

84409139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88942971-G-A

http://identifiers.org/hco/5/GRCh38#84409559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88942616-C-A

84409560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88942615-A-G

84409618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88942576-T-C

84410070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88942226-C-T

http://identifiers.org/hco/5/GRCh38#84410071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88942225-C-A

84410156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88942145-T-C

84410177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88942124-A-G

84410202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88942102-G-C

84410226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88942078-A-G

84410227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88942077-T-C

84410347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88941964-A-T

84410538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88941707-G-A

84410769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88940955-T-C

84434898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88932214-G-T

84435083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88932070-T-C

84435085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88932068-G-A

84435085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88932068-G-T

http://identifiers.org/hco/5/GRCh38#84444998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88930649-C-A

84444998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88930649-C-T

84445060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88930595-T-C

84446291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88927965-T-C

84446346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88927911-A-G

84446613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88925255-A-G

84446636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88925234-A-G

84446704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88925169-T-A

84446770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88918689-T-C

84446968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88918491-A-G

84446979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88918480-A-T

84447282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88917778-G-T

84447390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88917666-A-G

http://identifiers.org/hco/5/GRCh38#84447885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88916744-A-C

84447938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88916693-C-G

84467112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88904402-G-C

84467283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88903838-C-T

84467355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88903752-G-C

84467586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88903541-G-C

84467586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88903541-G-T

84467981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88903134-T-A

84468061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88903056-G-A

84468208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88902059-A-T

84468284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88901983-A-G

84468320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88901972-C-T

84468634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88901683-G-A

84468642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88901675-T-C

84468861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88901431-T-C

84468942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88901347-C-T

84469008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88901284-G-A

http://identifiers.org/hco/5/GRCh38#84469056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88901236-A-C

84469082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88901211-A-G

84469087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88901206-C-T

84469257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88900631-A-G

84469269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88900619-G-A

84469269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88900619-G-T

http://identifiers.org/hco/5/GRCh38#84469308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88900579-A-C

84469333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88900554-T-A

84469382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88900469-A-G

84469496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88900359-T-A

84469880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88900159-G-A

84470124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88899948-A-G

84470183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88899889-C-T

84470317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88899844-T-C

84470374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88899783-A-G

84470594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88899590-T-C

84470789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88899395-T-C

84470905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88899318-C-T

84471110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88899230-G-A

84472559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88898973-C-T

84473091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88898520-T-C

84473187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88898421-T-C

84473570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88898039-G-A

http://identifiers.org/hco/5/GRCh38#84473721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88897893-C-A

http://identifiers.org/hco/5/GRCh38#84473739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88897875-C-A

84473739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88897875-C-G

84473840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88897779-C-T

84473858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88897762-G-A

84474297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88897375-T-A

http://identifiers.org/hco/5/GRCh38#84474361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88897312-A-C

84474418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88897264-T-C

84475903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88892047-G-A

84476250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88891774-T-A

84476296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88891729-A-G

84476382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88891645-T-A

84476672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88891179-A-G

http://identifiers.org/hco/5/GRCh38#84476765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88891087-C-A

84477113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88890762-C-T

84477120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88890755-G-A

84477155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88890713-T-C

84477155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88890713-T-G

http://identifiers.org/hco/5/GRCh38#84477270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88890621-A-C

84477356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88890529-A-G

84477484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88890403-C-T

84478911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88887299-T-C

84478946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88887263-T-C

84479644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88886275-A-G

84485430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88882934-A-G

84485935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88873046-T-C

http://identifiers.org/hco/5/GRCh38#84485948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88873033-C-A

84485948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88873033-C-T

84489786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88867182-G-A

84489786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88867182-G-T

84489825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88867149-G-A

http://identifiers.org/hco/5/GRCh38#84489948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88867043-C-A

http://identifiers.org/hco/5/GRCh38#84490197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88866790-A-C

84490391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88866512-T-C

84490508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88866279-G-T

84490527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88866260-A-G

84490564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88866226-C-T

http://identifiers.org/hco/5/GRCh38#84490673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#88866122-C-A

84490728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40204
most severe consequence: non coding transcript exon variant
orthologous variants: 88866091-G-A