110567793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 53588947-C-T

110567834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53588988-A-G

http://identifiers.org/hco/10/GRCh38#110567909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#53589025-C-A

110567909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53589025-C-G

110567909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53589025-C-T

110568243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53589263-T-A

110568243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53589263-T-C

http://identifiers.org/hco/10/GRCh38#110568260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#53589267-C-A

110568260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53589267-C-G

110568260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53589267-C-T

http://identifiers.org/hco/10/GRCh38#110568276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53589283-C-A

110568276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53589283-C-T

110568277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53589284-T-C

110568277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53589284-T-G

110568368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53589348-T-A

110568495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 53589466-G-A

110568495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 53589466-G-C

110568495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 53589466-G-T

110568530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53589544-T-A

110568530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53589544-T-C

110568534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53589548-A-G

110568534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53589548-A-T

http://identifiers.org/hco/10/GRCh38#110568537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53589551-C-A

110568537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53589551-C-T

110568550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53589563-G-A

110568550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53589563-G-T

110568589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53589604-A-T

110568590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53589605-G-A

110568590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53589605-G-C

110568598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53589633-C-G

110568598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53589633-C-T

http://identifiers.org/hco/10/GRCh38#110568599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#53589634-C-A

110568599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53589634-C-T

110568616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53589650-A-G

http://identifiers.org/hco/10/GRCh38#110568637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53589670-C-A

110568734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53589717-C-T

110568865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53589841-A-G

http://identifiers.org/hco/10/GRCh38#110569038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53590018-C-A

110569038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53590018-C-G

110569038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53590018-C-T

110569043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53590023-T-C

110569098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53590061-A-T

110569197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53590152-G-A

110569214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53590171-A-G

110569214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53590171-A-T

110569839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53590570-A-G

http://identifiers.org/hco/10/GRCh38#110569956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#53590659-C-A

110570057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53590731-C-T

110570509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53591177-T-G

110570896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53591561-G-T

110571427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53595588-A-G

110571513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53595665-A-G

110571718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53595801-C-T

110571863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53595895-T-G

110573375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53601535-G-C

110573499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53602044-A-G

110573638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53602175-A-G

110573652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53602191-T-C

110573656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53602195-A-G

110573684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53602223-T-A

110573684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53602223-T-C

110573684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53602223-T-G

http://identifiers.org/hco/10/GRCh38#110573711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53602250-C-A

110573711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 53602250-C-T

110573784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53602323-T-A

110573784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53602323-T-C

110573784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53602323-T-G

110573799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53602337-A-G

110573800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53602338-G-T

110573872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53602404-G-A

110573872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53602404-G-T

110574030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53602516-G-A

110574549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53602798-T-G

110574632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53602904-C-T

110574871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53603098-A-G

110575025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53603262-A-G

110575185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53603397-T-G

110575234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53603437-G-T

110575429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53603621-A-T

110576604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53605222-T-A

110576854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53605704-G-A

110576874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53605712-A-G

110576890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53605725-T-A

http://identifiers.org/hco/10/GRCh38#110576927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53605762-C-A

110577149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53606054-A-G

110577250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53606243-T-C

110577339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53606410-T-G

110577365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53606436-T-C

http://identifiers.org/hco/10/GRCh38#110577384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53606455-A-C

110577384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53606455-A-G

110577412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53606483-C-G

110577707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53606777-A-G

110577707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53606777-A-T

http://identifiers.org/hco/10/GRCh38#110577789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53606854-C-A

110577789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53606854-C-G

110577789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53606854-C-T

110578540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53607110-A-G

http://identifiers.org/hco/10/GRCh38#110578583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53607155-C-A

110578733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53607326-G-A

110578735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53607328-A-G

110578953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53607674-G-T

http://identifiers.org/hco/10/GRCh38#110580831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53608947-C-A

110580842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53608958-G-A

110580842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53608958-G-T

110580879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53608995-A-G

110580882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53608998-A-G

http://identifiers.org/hco/10/GRCh38#110580999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53609115-C-A

110580999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53609115-C-T

110581932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53610171-G-T

110582159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53610386-A-G

110582178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53610403-T-A

110582463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53610934-A-G

110582463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53610934-A-T

110582466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53610937-T-G

110582550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53611023-T-G

http://identifiers.org/hco/10/GRCh38#110583328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53611432-C-A

http://identifiers.org/hco/10/GRCh38#110583344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53611448-C-A

110583579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53611678-G-T

110583994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53612051-C-T

110584172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53613369-A-G

110584177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 53613374-G-A

110584177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 53613374-G-C

110584179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 53613376-G-A

110584198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53613395-C-G

110584198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53613395-C-T

110584623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53613878-G-T

110584631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53613886-T-G

110584643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53613898-T-G

110584644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53613899-G-A

110584660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53613915-C-G

110584669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53613924-A-T

http://identifiers.org/hco/10/GRCh38#110584779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53614027-C-A

110584779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53614027-C-T

http://identifiers.org/hco/10/GRCh38#110589608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53616285-C-A

110589608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53616285-C-T

110589625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53616302-T-A

110589625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53616302-T-C

http://identifiers.org/hco/10/GRCh38#110589730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53616405-C-A

110589730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53616405-C-T

110589839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53616462-A-G

110589839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53616462-A-T

110589952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53616544-T-A

110589952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53616544-T-C

110590324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53617010-T-A

110590340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53617026-G-T

110590364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53617053-G-T

110590365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53617054-C-T

110590507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53617193-T-C

110590649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53617424-T-A

110590708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53617485-G-A

110590708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53617485-G-T

110591223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53617891-A-G

110591228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53617896-G-T

http://identifiers.org/hco/10/GRCh38#110591264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53617927-C-A

110591266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53617929-A-G

110591274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53617941-T-C

http://identifiers.org/hco/10/GRCh38#110591427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53618002-A-C

110591427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53618002-A-G

110591427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53618002-A-T

110591585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53618119-G-A

110592624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53619338-A-G

110592892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53619754-G-A

http://identifiers.org/hco/10/GRCh38#110592935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53619796-C-A

110592990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53619825-A-G

110593007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53619842-T-G

110593056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53619901-C-T

110596091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53622141-G-A

http://identifiers.org/hco/10/GRCh38#110596258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53622256-C-A

110596273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53622270-G-T

110596316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53622320-G-A

110596316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53622320-G-T

110597160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53622936-G-T

110597262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53623014-G-T

110597293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53623041-G-T

110597797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53623683-A-G

http://identifiers.org/hco/10/GRCh38#110597876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53623847-C-A

110597876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53623847-C-T

110597989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53623960-G-T

http://identifiers.org/hco/10/GRCh38#110598008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53623980-C-A

110598075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53624036-A-G

http://identifiers.org/hco/10/GRCh38#110598248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53624211-A-C

110598248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53624211-A-G

110598377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53624329-G-A

110598377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53624329-G-C

110598377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53624329-G-T

110598385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53624337-T-A

110598385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53624337-T-C

110599551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53624703-A-G

110599551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53624703-A-T

110599584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53624745-T-C

110599728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53624886-G-A

http://identifiers.org/hco/10/GRCh38#110600419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53627105-C-A

110600586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53627262-G-A

110600586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53627262-G-C

110600586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53627262-G-T

110600640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53627313-G-C

110600640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53627313-G-T

http://identifiers.org/hco/10/GRCh38#110600675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53627339-C-A

110600675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53627339-C-G

110600675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53627339-C-T

110600683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53627353-G-T

110600684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53627354-G-T

110600694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53627364-A-G

110600694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53627364-A-T

http://identifiers.org/hco/10/GRCh38#110600954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53627653-C-A

110600954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53627653-C-T

110601169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53628117-T-C

110601376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53628899-G-A

110601376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53628899-G-C

110601412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53628933-A-G

110601477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53629005-A-G

110601746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53629302-T-C

110601803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53629359-A-G

110601833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53629389-A-G

110601878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53629434-C-T

110601893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53629459-T-C

110601905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53629471-C-T

110601907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53629473-T-C

http://identifiers.org/hco/10/GRCh38#110601912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53629478-C-A

110601917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53629483-T-G

110601927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53629504-A-G

110601952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53629516-T-C

110602278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53629775-G-A

110602305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53629802-A-G

110602333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53629837-T-C

110602692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53630175-C-G

110602693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53630176-T-A

http://identifiers.org/hco/10/GRCh38#110602705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53630188-C-A

110602706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53630189-A-G

110602718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53630201-A-G

110602718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53630201-A-T

110602794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53630263-G-C

110602872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53630339-T-C

110602929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53630396-T-C

110603085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53632179-C-T

http://identifiers.org/hco/10/GRCh38#110603123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53632218-C-A

110603123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53632218-C-T

110603203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53632294-T-A

110603203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53632294-T-C

110603390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53632464-G-T

http://identifiers.org/hco/10/GRCh38#110603392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53632466-C-A

110603392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53632466-C-G

110603421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53632495-A-G

110603425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53632502-C-G

110603557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53632574-A-G

110603561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53632578-T-C

110603561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53632578-T-G

110604178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53633076-A-G

110604211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53633122-T-C

http://identifiers.org/hco/10/GRCh38#110604290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53633197-C-A

110604290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53633197-C-T

http://identifiers.org/hco/10/GRCh38#110604394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53633299-A-C

110604401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53633310-T-C

110604401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53633310-T-G

110604413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53633322-G-A

110604413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53633322-G-T

http://identifiers.org/hco/10/GRCh38#110604458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53633366-C-A

110604458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53633366-C-T

110604606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53633489-T-A

110604606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53633489-T-G

110604648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2468
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53633529-G-A