http://identifiers.org/hco/10/GRCh38#45727188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116184985-C-A

45727188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 116184985-C-G

45727188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 116184985-C-T

http://identifiers.org/hco/10/GRCh38#45727199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116184996-C-A

45727199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 116184996-C-T

45727201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 116184998-T-C

45727201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 116184998-T-G

45727236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116185034-T-A

45727236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116185034-T-C

45727236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116185034-T-G

http://identifiers.org/hco/10/GRCh38#45727303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116185071-A-C

45727303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116185071-A-G

http://identifiers.org/hco/10/GRCh38#45727555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116185305-C-A

45727555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116185305-C-G

45727555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116185305-C-T

http://identifiers.org/hco/10/GRCh38#45727668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116185357-C-A

45727668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116185357-C-G

45727668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116185357-C-T

45728035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116185697-G-A

45728430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116185789-T-G

45728838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116185892-C-T

45729043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116186096-T-C

45729392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116186444-T-C

45729620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116186848-T-C

45731040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116188250-G-A

45732107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116188620-T-C

45732399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116188909-T-A

45738024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116190950-T-A

45739923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116192896-T-C

45739972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116192938-T-C

45739972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116192938-T-G

45740183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116193117-A-G

45740255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116193188-A-G

45740287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116193208-T-A

45740287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116193208-T-C

45740352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116193257-A-G

45740362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116193266-G-A

45740362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116193266-G-T

45740405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116193311-G-A

45740509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116193387-A-T

45740559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116193436-T-C

45743257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116194579-G-C

45743257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116194579-G-T

45743552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116194875-T-C

45743578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116194901-A-G

http://identifiers.org/hco/10/GRCh38#45743585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116194906-C-A

45743614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116194934-T-G

http://identifiers.org/hco/10/GRCh38#45743618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116194938-C-A

45743618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116194938-C-G

45743618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116194938-C-T

45743655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116194969-C-G

45743655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116194969-C-T

45744721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116195525-A-G

45744725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116195529-T-C

45744790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116195593-G-A

45744809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116195610-T-C

45744897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116195695-G-A

http://identifiers.org/hco/10/GRCh38#45745051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116195822-C-A

45745051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116195822-C-T

45745485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116196362-A-G

45745564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116196436-C-T

45746227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116196619-A-G

45746481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116196826-T-C

http://identifiers.org/hco/10/GRCh38#45746503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116196848-C-A

45746503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116196848-C-G

45746595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116196909-T-C

45746633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116196947-A-G

45746655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116196969-T-G

45746716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116197030-T-C

45746744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116197149-G-A

45749943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116197372-C-T

45750008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116197411-C-T

45750029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116197432-A-G

http://identifiers.org/hco/10/GRCh38#45750290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116198316-C-A

45750290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116198316-C-T

http://identifiers.org/hco/10/GRCh38#45750347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116198367-C-A

45750347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116198367-C-T

45750350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116198378-C-T

45750380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116198408-G-A

45750403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116198428-G-A

45750584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116198597-C-T

45750747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116198773-G-A

45750747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116198773-G-C

45750820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116198840-G-A

http://identifiers.org/hco/10/GRCh38#45751261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116199978-A-C

45751261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116199978-A-G

45751353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116200016-G-A

45751353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116200016-G-T

45751362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116200025-A-G

http://identifiers.org/hco/10/GRCh38#45751365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116200028-A-C

45751365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116200028-A-G

http://identifiers.org/hco/10/GRCh38#45751370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116200033-C-A

45751370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116200033-C-G

45751370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116200033-C-T

http://identifiers.org/hco/10/GRCh38#45751388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116200051-C-A

http://identifiers.org/hco/10/GRCh38#45751407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116200069-C-A

45751407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116200069-C-G

45751475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116200138-C-G

45751475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116200138-C-T

45751566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116200225-C-T

45751668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116200287-G-A

45751668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116200287-G-C

45752556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116201354-C-T

http://identifiers.org/hco/10/GRCh38#45752620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116201414-C-A

http://identifiers.org/hco/10/GRCh38#45752637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116201431-C-A

45752637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116201431-C-G

45752715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116201504-A-G

45752715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116201504-A-T

http://identifiers.org/hco/10/GRCh38#45752741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116201521-C-A

45752760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116201541-A-G

45752760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116201541-A-T

45752772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116201550-T-A

45752772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116201550-T-C

45752772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116201550-T-G

45752773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116201551-A-G

45752797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116201572-A-G

http://identifiers.org/hco/10/GRCh38#45752822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116201593-C-A

45752822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116201593-C-T

45752855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116201623-A-G

45752884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116201652-C-T

http://identifiers.org/hco/10/GRCh38#45752889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116201657-A-C

45752889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116201657-A-G

45752893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116201661-T-C

http://identifiers.org/hco/10/GRCh38#45753254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116202008-C-A

45753267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116202021-G-A

45753267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116202021-G-C

45754496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116203398-A-G

45754496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116203398-A-T

45754505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116203407-T-A

45754505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116203407-T-C

45754894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116204270-C-T

45754923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116204294-C-G

45754923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116204294-C-T

http://identifiers.org/hco/10/GRCh38#45755009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116204380-A-C

45755009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116204380-A-G

http://identifiers.org/hco/10/GRCh38#45755075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116204455-C-A

45755075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116204455-C-G

45755075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116204455-C-T

http://identifiers.org/hco/10/GRCh38#45755224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116204597-C-A

45755224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116204597-C-T

45755446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116204817-T-C

45755626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116204952-C-T

45756805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116205848-G-A

45757110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116206282-G-A

45757110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116206282-G-C

45757110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116206282-G-T

45757187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116206356-T-G

45757345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116206869-G-A

45757473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116206961-C-G

45757584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116207056-C-T

45759120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116207910-G-A

45759197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116208406-A-G

45759549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116208728-G-A

45759549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116208728-G-C

45759568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116208746-C-G

45759568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116208746-C-T

45761936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116212282-C-T

45762049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116212394-C-G

45762049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116212394-C-T

http://identifiers.org/hco/10/GRCh38#45762088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116212431-A-C

45762948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116212714-G-C

45763126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116212867-T-C

45763126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116212867-T-G

45763149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116212890-T-C

45763172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116212905-C-G

45763245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116212941-T-C

http://identifiers.org/hco/10/GRCh38#45763436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116213106-C-A

45763436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116213106-C-G

45763436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116213106-C-T

http://identifiers.org/hco/10/GRCh38#45763569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116213233-A-C

45764488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116213419-G-A

45764763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116213658-G-T

45764874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116213772-T-A

45764901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116213798-C-G

http://identifiers.org/hco/10/GRCh38#45765022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116214115-C-A

45765261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116214454-A-G

45765318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116214508-G-A

45765647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116215059-T-A

45765647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116215059-T-G

45765669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116215083-G-C

45765839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116215251-G-A

http://identifiers.org/hco/10/GRCh38#45765904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116215317-C-A

45765904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116215317-C-T

http://identifiers.org/hco/10/GRCh38#45765935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116215349-C-A

45765935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116215349-C-T

45769499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116218458-G-A

45769499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116218458-G-T

45769523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116218482-T-A

45769523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116218482-T-C

45769546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116218505-C-G

45769546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116218505-C-T

45769568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116218527-T-C

45769580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116218545-A-T

http://identifiers.org/hco/10/GRCh38#45769583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116218548-C-A

45770544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116219403-A-T

45770568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116219427-G-T

45770610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116219466-G-A

http://identifiers.org/hco/10/GRCh38#45770822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116219675-C-A

45770866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116219691-C-T

45771061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116219855-G-A

45771061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116219855-G-T

45771560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116220022-C-T

45771582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116220044-G-A

45771591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116220053-G-C

45771591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116220053-G-T

45771610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116220070-A-G

45771758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 116220337-G-A

45771758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 116220337-G-T

45771772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116220351-G-A

45771898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116220620-G-A

45771963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116220681-G-A

45772000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116220714-A-G

45772016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116220730-G-T

45772161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116220874-G-A

45772757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116221060-G-A

45772790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116221090-C-T

http://identifiers.org/hco/10/GRCh38#45772924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116221222-C-A

45773004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116221305-G-A

45773009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116221310-G-A

45773040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116221364-A-G

45773065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116221392-T-C

45773073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116221399-A-G

45773158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116221470-G-T

45773246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116221543-G-A

45773246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116221543-G-T

45773277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116221572-G-A

45773410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116221702-A-G

45775970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116222036-G-A

45775970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116222036-G-C

45775975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116222041-C-T

45776394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116222365-C-T

45776931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116222806-A-G

45777109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116222907-G-C

45777134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116222933-T-G

45777191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116222990-T-G

45777205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116223004-G-A

45777205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116223004-G-C

45777209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116223008-A-G

http://identifiers.org/hco/10/GRCh38#45777336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116223129-C-A

45777336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116223129-C-G

45777336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 116223129-C-T

45777341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116223134-T-G

45777343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116223136-G-C

45777343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116223136-G-T

45777359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116223152-T-C

45777368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116223161-T-G

http://identifiers.org/hco/10/GRCh38#45777525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116223361-C-A

45777525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116223361-C-T

45777527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116223363-C-G

45777527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116223363-C-T

45777539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116223375-G-T

45777671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116223687-C-T

45777720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116223771-T-G

45777813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116223852-T-C

45777889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116223921-C-T

45778173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116224185-C-T

45778312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116224278-A-G

http://identifiers.org/hco/10/GRCh38#45778384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116224381-C-A

45778384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116224381-C-T

45778556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116224564-A-T

45778958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116224942-A-T

45778961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116224945-T-C

45778969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116224953-G-A

45779169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116225186-G-A

45779198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116225218-T-C

45779283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116225295-G-A

45779450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116225404-C-T

45779550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116225496-A-G

45784474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116231010-C-G

45784480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116231016-T-C

45784481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116231017-G-A

45784651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116231137-T-C

45784800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116231353-C-T

45785474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116231976-T-C

45785482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116231983-C-T

45785545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116232046-T-A

http://identifiers.org/hco/10/GRCh38#45785648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116232146-A-C

45785648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116232146-A-T

45785660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116232158-C-T

45785820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116232296-T-C

45785820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116232296-T-G

45785900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116232351-A-G

http://identifiers.org/hco/10/GRCh38#45786098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116232585-C-A

45786433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116233013-G-A

45786433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116233013-G-T

http://identifiers.org/hco/10/GRCh38#45786451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116233028-C-A

45786527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116233094-C-T

45786548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116233124-G-T

45786728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116233306-T-C

45786893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116233461-G-T

http://identifiers.org/hco/10/GRCh38#45786965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116233507-A-C

45786965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116233507-A-G

45787036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 116233578-C-T

45787920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116234216-T-C

45788219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116234608-T-C

45788515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116234871-G-A

45788707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116235296-C-T

45788837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116235571-C-T

http://identifiers.org/hco/10/GRCh38#45788966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116235698-C-A

45789035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116235773-A-G

45789048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116235786-G-A

45789256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116235982-C-T

45789316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116236042-C-T

45789327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116236053-G-A

45789393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116236119-G-T

45789758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116236921-T-G

45789911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237050-T-C

45789911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237050-T-G

45790185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237299-G-A

45790216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237330-T-C

45790216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237330-T-G

45790286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237382-G-C

45790657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237732-A-T

45790860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237913-C-T

http://identifiers.org/hco/10/GRCh38#45791215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116238281-C-A

45791215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116238281-C-T

http://identifiers.org/hco/10/GRCh38#45791699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116238779-A-C

45791871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116238912-C-T

45791959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116239001-G-A

45791967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116239008-G-A

45792148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116239195-G-T

http://identifiers.org/hco/10/GRCh38#45792165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116239202-A-C

45792165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116239202-A-G

45792165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116239202-A-T

http://identifiers.org/hco/10/GRCh38#45792168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116239205-A-C

45792177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116239214-T-G

45792222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116239257-C-G

45792298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116239333-C-G

45792298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116239333-C-T

45792314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116239349-T-C

45792388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116239423-T-G

45792466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116239511-G-A

45792677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116239673-T-C

45792713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116239712-G-A

45792724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116239722-G-T

45792808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23414
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116239795-G-T