57109765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77555337-C-G

57109765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77555337-C-T

57109783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77555340-C-T

http://identifiers.org/hco/4/GRCh38#57109784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77555341-A-C

57109785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77555342-G-A

57109785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77555342-G-T

57109787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77555344-G-A

57109787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77555344-G-T

http://identifiers.org/hco/4/GRCh38#57109798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77555355-C-A

57109798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77555355-C-T

57109853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77555363-G-A

57109853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77555363-G-T

57109854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77555364-G-T

57109858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77555368-G-A

57109858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77555368-G-C

57109858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77555368-G-T

http://identifiers.org/hco/4/GRCh38#57109883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#77555393-C-A

57109883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 77555393-C-G

57109883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 77555393-C-T

http://identifiers.org/hco/4/GRCh38#57109885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#77555395-C-A

57109885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 77555395-C-T

57109888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 77555398-G-A

57109888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 77555398-G-T

57109903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 77555413-T-A

57109903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 77555413-T-C

http://identifiers.org/hco/4/GRCh38#57109935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#77555445-C-A

57109935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 77555445-C-T

57109947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 77555457-G-A

57109947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 77555457-G-T

http://identifiers.org/hco/4/GRCh38#57109949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#77555459-C-A

57109949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 77555459-C-T

57109950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 77555460-G-A

57109950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 77555460-G-T

57110001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555511-G-A

57110001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555511-G-C

57110001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555511-G-T

57110025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555535-G-A

57110025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555535-G-T

http://identifiers.org/hco/4/GRCh38#57110042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#77555552-C-A

57110042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555552-C-G

57110042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555552-C-T

57110046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555556-G-A

57110046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555556-G-C

57110046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555556-G-T

57110053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555563-G-A

57110053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555563-G-C

57110053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555563-G-T

57110091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555601-G-A

57110091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555601-G-C

57110091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555601-G-T

http://identifiers.org/hco/4/GRCh38#57110094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#77555604-C-A

57110094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555604-C-G

57110094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555604-C-T

http://identifiers.org/hco/4/GRCh38#57110115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#77555625-C-A

57110115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555625-C-G

57110115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555625-C-T

http://identifiers.org/hco/4/GRCh38#57110156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#77555666-C-A

57110156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555666-C-G

57110156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555666-C-T

57110157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555667-G-A

57110157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555667-G-C

57110157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555667-G-T

57110169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555679-A-T

57110178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555688-G-A

57110178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555688-G-C

57110178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555688-G-T

57110187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555697-G-A

57110187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555697-G-T

57110218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555728-G-A

57110218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555728-G-T

57110226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555736-G-A

57110226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555736-G-T

57110274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555784-G-A

57110274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555784-G-C

57110274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555784-G-T

57110279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555789-A-G

57110279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555789-A-T

57110291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555801-G-A

57110291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555801-G-T

http://identifiers.org/hco/4/GRCh38#57110307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#77555817-C-A

57110307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555817-C-T

http://identifiers.org/hco/4/GRCh38#57110309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#77555819-C-A

57110309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555819-C-G

57110309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555819-C-T

http://identifiers.org/hco/4/GRCh38#57110312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#77555822-C-A

57110312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555822-C-T

57110331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555841-G-A

57110331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555841-G-C

57110331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555841-G-T

57110336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555843-G-A

57110336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555843-G-T

http://identifiers.org/hco/4/GRCh38#57110337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#77555844-C-A

57110337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555844-C-T

57110355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555862-G-A

57110355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555862-G-T

57110365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555868-G-A

57110365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555868-G-T

57110371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555874-G-A

57110371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555874-G-C

57110371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555874-G-T

57110372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555875-G-A

57110372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555875-G-C

57110372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77555875-G-T

57110402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77555909-G-A

57110402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77555909-G-T

http://identifiers.org/hco/4/GRCh38#57110426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77555932-C-A

57110426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77555932-C-T

57110431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77555937-G-A

57110431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77555937-G-T

http://identifiers.org/hco/4/GRCh38#57110441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77555946-C-A

57110441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77555946-C-G

57110441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77555946-C-T

http://identifiers.org/hco/4/GRCh38#57110455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77555959-C-A

57110455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77555959-C-G

57110455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77555959-C-T

57110498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77555989-G-A

57110498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77555989-G-C

57110498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77555989-G-T

http://identifiers.org/hco/4/GRCh38#57110502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77555993-C-A

57110502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77555993-C-T

57110503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77555994-C-T

57110513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77556004-G-T

http://identifiers.org/hco/4/GRCh38#57110518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#77556009-C-A

57110518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77556009-C-G

57110519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77556010-G-A

57110519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77556010-G-C

57110526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77556017-T-A

57110526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77556017-T-C

57110526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77556017-T-G

57110529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77556020-T-A

57110532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77556023-C-T

57110533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77556024-G-T

57110548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77556033-G-A

57110548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77556033-G-C

57110567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77556047-C-T

57110588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77556067-C-G

57110600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77556078-A-G

57110613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77556086-A-T

57110648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77556120-C-T

57110649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77556121-C-G

57110663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77556129-C-G

57110664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77556130-G-A

57110673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77556139-G-A

57110709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77556173-G-A

http://identifiers.org/hco/4/GRCh38#57111599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77564384-A-C

57111600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77564385-C-T

57111671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77564453-T-A

57111672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77564454-T-A

57111695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77564469-T-C

57111750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77564496-C-G

57111773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77564519-A-G

57111849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77564602-A-G

57111849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77564602-A-T

57112285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77564693-G-T

57112292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77564705-T-C

57112363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77564775-G-A

57112497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77564909-G-A

57112497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77564909-G-T

57112547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77564960-G-A

57112612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77565021-C-T

57112692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77565096-G-A

57112812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77565292-A-G

57112878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77565378-T-G

57113669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77568181-C-T

57113840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77568335-T-A

http://identifiers.org/hco/4/GRCh38#57113856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77568351-A-C

57113947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77568427-T-C

57113960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77568657-G-A

57114029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77568726-C-G

57114029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77568726-C-T

57114044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77568741-C-T

57114066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77568762-A-G

57114066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77568762-A-T

57114081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77568777-A-G

57114134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77568823-G-T

57114327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77569014-T-C

57114709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77569081-A-G

57114738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77569105-G-A

57114781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77569145-C-T

57114783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77569147-A-G

57114825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77569196-T-C

57114889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77569261-G-A

57114946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77569314-C-G

57114972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77569340-C-T

57114978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77569346-C-T

57115021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77569384-G-A

57115153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77569530-G-A

http://identifiers.org/hco/4/GRCh38#57115182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#77569560-A-C

57115182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77569560-A-G

http://identifiers.org/hco/4/GRCh38#57115319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77570444-C-A

57115381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77570490-T-A

57115507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77570588-G-A

57116479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77572420-A-G

57116509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77572447-A-G

57116525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77572464-A-G

57116551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77572490-A-G

57116623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77572554-G-C

57116634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77572565-G-T

57116651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77572588-A-G

57116666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77572603-A-G

57116676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77572613-G-A

57116732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77572655-G-T

57116883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77572796-A-G

57116908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77572821-G-A

http://identifiers.org/hco/4/GRCh38#57116973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77572886-C-A

57116973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77572886-C-T

57117015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77572928-T-C

57117039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77572950-G-A

57117040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77572951-T-C

57117049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77572960-T-C

57117058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77572969-A-G

57117071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77573005-T-C

http://identifiers.org/hco/4/GRCh38#57117204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77573142-A-C

http://identifiers.org/hco/4/GRCh38#57117541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77573437-A-C

57117688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77574129-A-G

57117689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77574130-G-C

57117719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77574159-T-C

57117755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77574194-G-A

57117826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77574223-C-T

57117862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77574252-G-A

57117884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77574275-G-A

57117940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77574331-T-A

57118145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77574494-C-T

57118158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77574507-G-A

57118248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77575366-G-T

http://identifiers.org/hco/4/GRCh38#57118392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77575474-A-C

57118673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77575912-G-A

57118688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77575938-C-T

http://identifiers.org/hco/4/GRCh38#57118698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77575948-C-A

57118824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77576151-A-G

57118887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77576248-G-C

57118985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77576342-T-C

http://identifiers.org/hco/4/GRCh38#57119014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77576374-C-A

57119103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77576434-T-C

57119285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77576608-T-C

57119288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77576610-G-A

57119328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77576640-C-G

57119495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77576808-A-G

57119545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77576868-C-T

57119564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77576887-G-A

57119594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77576915-A-G

57119674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77577014-T-C

57119675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77577015-G-A

57119717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77577058-C-T

57124258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77578066-A-T

57124339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77578150-G-A

57124668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77578480-T-G

http://identifiers.org/hco/4/GRCh38#57124700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77578512-A-C

57124909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77578719-G-A

57124909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77578719-G-T

http://identifiers.org/hco/4/GRCh38#57125100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77578911-C-A

57125100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77578911-C-G

57125175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77579228-A-G

57125269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77579319-A-G

57125475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77579514-G-T

57125510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77579558-C-T

57125511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77579559-G-A

57125552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77579589-G-T

57125592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77579629-G-A

57125654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77579691-G-C

57129011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77580110-T-C

57129348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77580464-T-C

57129418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77580584-C-T

57129428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77580594-A-T

57129430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77580601-G-A

57132276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77581507-T-G

57132350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77581579-T-C

57132475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77581698-C-G

57132551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77581767-C-T

57132832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77581989-C-T

57133059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77582182-G-A

57133082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77582205-G-A

57133287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77582398-A-G

57133301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77582412-C-G

57133301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77582412-C-T

57133303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77582414-T-C

57133430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77582543-C-G

57133493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77582598-C-T

57133578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77582680-T-C

57133634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77582740-G-C

57134022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77583090-G-A

57134053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77583118-G-T

57134145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77583218-A-G

57134156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77583229-A-G

57134390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77583436-G-C

57134459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77583521-T-A

57134501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77583579-C-T

57144182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77583811-G-C

57144347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77583959-G-A

http://identifiers.org/hco/4/GRCh38#57144356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77583968-A-C

57144441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77584054-G-A

57146229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77587694-C-T

57146279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77587746-T-C

57146444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77587886-G-A

57146487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77587920-C-T

57146554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77587986-G-A

57146605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77588034-T-C

http://identifiers.org/hco/4/GRCh38#57146690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77588506-C-A

57146710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77588512-C-T

57147037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77588823-G-A

57147074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77588852-T-G

http://identifiers.org/hco/4/GRCh38#57147167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77589021-A-C

57147167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77589021-A-G

http://identifiers.org/hco/4/GRCh38#57147304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77589173-C-A

http://identifiers.org/hco/4/GRCh38#57147440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77589285-C-A

57148967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77589970-C-G

57149216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77590232-A-T

57149232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77590248-A-G

57149245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77590262-A-G

57149273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77590291-T-C

57149534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77590553-T-C

57149683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77590702-A-G

57149736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77590755-C-T

57149779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77590798-G-T

57149832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77590850-G-A

57149943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77590958-C-G

57149965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77590980-T-C

57150081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77591096-A-G

http://identifiers.org/hco/4/GRCh38#57150384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77591380-C-A

57150384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77591380-C-T

57150391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77591387-T-A

http://identifiers.org/hco/4/GRCh38#57153766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77592261-A-C

57153766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77592261-A-T

57155176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77594391-A-G

57155464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77594703-G-C

57155471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77594710-G-A

57155471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77594710-G-C

57155671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77594897-C-G

57155671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77594897-C-T

57155689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77595015-G-A

57155689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77595015-G-T

57155766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77595110-C-T

57155793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77595137-C-G

57156038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77595388-G-A

57156205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77595548-G-A

57156205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77595548-G-T

http://identifiers.org/hco/4/GRCh38#57156346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#77595672-C-A

57156349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 77595675-A-G

57156542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77595809-T-A

57156542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77595809-T-C

57156782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77596068-C-T

57157092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77596985-A-T

57157103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77596996-C-T

57157417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77597243-G-A

57157484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77597307-T-C

57157593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77597413-G-A

57157749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77597531-C-T

57157852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77597634-C-T

57157912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77597694-C-T

57157997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77597776-T-C

57158070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77597854-G-A

57158200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77598095-C-T

57159382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77599530-G-A

57159449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77599597-T-C

57159783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77599925-A-G

http://identifiers.org/hco/4/GRCh38#57160928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77602042-C-A

57160928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77602042-C-T

57160951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77602065-T-C

57162616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77606367-C-T

57162777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77606544-A-G

57162800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77606564-G-A

57162886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77606644-C-T

57162893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77606651-C-T

http://identifiers.org/hco/4/GRCh38#57162984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77606734-A-C

http://identifiers.org/hco/4/GRCh38#57162989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77606739-C-A

http://identifiers.org/hco/4/GRCh38#57162994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77606744-C-A

57163215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77607333-A-G

57163356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77607448-C-T

57163733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77607827-G-A

57163797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77607884-G-T

57164160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77608384-G-T

57164170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77608394-G-A

http://identifiers.org/hco/4/GRCh38#57164195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#77608419-C-A

57164239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77608463-G-T

57166177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77609142-T-G

57166178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77609143-G-A

57166202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77609164-G-A

57166242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77609201-A-T

57166276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77609225-C-T

57166306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77609255-G-A

http://identifiers.org/hco/4/GRCh38#57166314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77609263-C-A

57166370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77609319-C-T

57166506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77609444-G-A

57166541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77609477-T-G

http://identifiers.org/hco/4/GRCh38#57166555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77609489-C-A

57166555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77609489-C-G

57166988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77609692-G-A

57167126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77609820-A-G

57167608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77610379-G-A

57167712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77610462-C-G

http://identifiers.org/hco/4/GRCh38#57167892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77610625-A-C

57167958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77610661-T-C

57168874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77612663-A-G

57169082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77612848-C-G

57169082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77612848-C-T

57169173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77612936-C-T

57169187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77612951-T-C

57169462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77613230-C-G

57169509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77613277-A-G

57169518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77613286-A-G

57169591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77613341-C-T

57169653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77613438-A-T

57172175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77613915-T-C

57172197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77613937-A-G

57172363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77614107-A-G

57174170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77614291-A-G

57174260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77614364-G-A

57174260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77614364-G-C

57174260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77614364-G-T

57174516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77614620-T-C

http://identifiers.org/hco/4/GRCh38#57174584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77614688-A-C

57174584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77614688-A-T

57174736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77614833-T-A

57175270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77615261-G-A

57175361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77615298-T-C

57175443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77615387-G-A

57175764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77615667-G-A

57175863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77615747-A-T

57175985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77616086-C-T

57176194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77616291-T-C

57176245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77616342-A-G

57176626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77616821-G-A

57176835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77617012-C-T

57176845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77617022-A-G

http://identifiers.org/hco/4/GRCh38#57176905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77617075-C-A

57177135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77617253-C-T

57177409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77617509-A-T

57177429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77617517-G-A

http://identifiers.org/hco/4/GRCh38#57177460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77617545-A-C

57177751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77617896-T-C

57177758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77617903-G-A

57177758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77617903-G-T

http://identifiers.org/hco/4/GRCh38#57177770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77617944-A-C

57177832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77618004-G-C

57177999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77618099-T-C

57178142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77618255-G-A

57178230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77618340-T-C

57178242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77618352-T-A

57178271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77618379-A-G

57178356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77618478-T-C

57178840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77619459-T-A

http://identifiers.org/hco/4/GRCh38#57179047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77619663-C-A

57179154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77619751-G-A

57179154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77619751-G-T

57179162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77619759-A-G

57179168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77619765-A-G

http://identifiers.org/hco/4/GRCh38#57179172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77619769-C-A

57179172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77619769-C-T

57179310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77619896-G-C

57179310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77619896-G-T

57179312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77619898-T-C

57179338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77619923-T-C

57179376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77619959-G-T

57179397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77619976-A-G

57179405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77619984-G-T

http://identifiers.org/hco/4/GRCh38#57179465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77620046-C-A

57179727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77620249-A-G

57181167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77620775-G-A

57181296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77620906-A-G

57181432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77621049-A-T

57181541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77621152-G-A

57181734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77621346-T-C

57181980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77621588-C-T

57182103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77621707-A-T

57182406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77622002-G-A

57182538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77622127-G-A

57182884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77622444-G-C

57182919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77622460-G-A

57183033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77622576-G-A

http://identifiers.org/hco/4/GRCh38#57184647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77625220-C-A

57184647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77625220-C-G

57184666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77625239-C-G

57184666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77625239-C-T

57185238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77625772-C-T

57185307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77625838-G-C

57185359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77625892-T-C

57186634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77628132-G-A

57186641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77628139-G-A

57186705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77628182-C-G

57186796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77628241-G-A

57186807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77628252-G-A

57186818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77628263-G-C

57189073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77631041-T-G

57189127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77631087-T-C

57189156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77631128-C-G

57189316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77631284-T-A

57189316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77631284-T-C

57189317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77631285-G-A

57189317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77631285-G-T

http://identifiers.org/hco/4/GRCh38#57189408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77631368-A-C

57189408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77631368-A-G

http://identifiers.org/hco/4/GRCh38#57189428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77631388-C-A

57189428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77631388-C-T

http://identifiers.org/hco/4/GRCh38#57190447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77632061-A-C

57190671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77632317-C-T

57191037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77632679-G-T

57191073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77632712-G-A

57191073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77632712-G-C

57191189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77632804-C-G

57191189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77632804-C-T

57191240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77632917-C-G

57191240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77632917-C-T

57191488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77633133-A-G

57191790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77633428-T-C

57192339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77633864-C-T

57192379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77633902-T-C

57192483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77633999-T-C

57192727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77634746-C-T

57193282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77634953-A-G

57193285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77634958-A-G

57193305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77634974-C-T

57193522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77635174-A-G

http://identifiers.org/hco/4/GRCh38#57193574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77635225-C-A

57193574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77635225-C-T

57193612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77635277-C-G

57193834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77635490-T-A

57194384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77636027-C-T

57194459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77636109-G-A

57194525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77636167-A-G

57194964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77636277-C-T

57195047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77636360-G-A

http://identifiers.org/hco/4/GRCh38#57195053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77636366-C-A

57195595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

57195595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

57195621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

57195694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

57197339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77637139-G-A

57197414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77637192-A-G

57197973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77637956-G-A

http://identifiers.org/hco/4/GRCh38#57198771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77639500-C-A

57198806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77639535-T-C

57199094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77639823-T-C

57199094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77639823-T-G

57200424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77640489-G-C

57200488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77640548-G-C

57200511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77640565-G-T

57200557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77640616-G-C

57200632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77640695-A-G

57200750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77640811-G-T

http://identifiers.org/hco/4/GRCh38#57200859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77641682-C-A

57200859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77641682-C-G

57200859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77641682-C-T

57201063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77641880-A-T

57201108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77641925-T-A

57201108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77641925-T-C

http://identifiers.org/hco/4/GRCh38#57201113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77641930-C-A

57201126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77641943-G-T

57201180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non coding transcript exon variant
orthologous variants: 77641994-C-T

57201248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77642062-T-C

57201366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77642181-G-T

57201425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77642231-T-A

57201452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77642254-T-C

57203170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77644646-G-A

http://identifiers.org/hco/4/GRCh38#57203245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77644720-C-A

57203303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77644775-T-C

57203308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77644780-G-T

57203315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77644787-A-G

57203565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77645009-C-T

57203629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77645078-C-G

57204073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77645512-A-T

57204158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77645621-G-A

57204308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77645806-A-G

57204958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77646770-G-A

57204971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77646781-A-G

57204971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77646781-A-T

57205045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77646843-T-C

http://identifiers.org/hco/4/GRCh38#57205091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77646892-C-A

57205144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non coding transcript exon variant
orthologous variants: 77646940-G-T

http://identifiers.org/hco/4/GRCh38#57205199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77646995-A-C

57205199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non coding transcript exon variant
orthologous variants: 77646995-A-G

http://identifiers.org/hco/4/GRCh38#57205291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77647088-C-A

57205373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non coding transcript exon variant
orthologous variants: 77647174-A-G

57205590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non coding transcript exon variant
orthologous variants: 77647396-A-G

57205591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non coding transcript exon variant
orthologous variants: 77647397-T-C

http://identifiers.org/hco/4/GRCh38#57205638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77647445-C-A

57205686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non coding transcript exon variant
orthologous variants: 77647491-T-C

57205773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non coding transcript exon variant
orthologous variants: 77647575-G-C

57205907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non coding transcript exon variant
orthologous variants: 77647710-T-C

57206247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non coding transcript exon variant
orthologous variants: 77648023-G-T

http://identifiers.org/hco/4/GRCh38#57206271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77648048-C-A

57206404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non coding transcript exon variant
orthologous variants: 77648160-A-G

57206488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non coding transcript exon variant
orthologous variants: 77648238-A-G

57206689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non coding transcript exon variant
orthologous variants: 77648402-A-G

57206783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non coding transcript exon variant
orthologous variants: 77648492-C-T

57206985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40296
most severe consequence: non coding transcript exon variant
orthologous variants: 77648665-G-T