http://identifiers.org/hco/14/GRCh38#52552911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45457251-C-A

52552911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45457251-C-T

52552969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45457301-G-C

52552976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45457308-C-T

52553012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45457342-G-C

52553012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45457342-G-T

http://identifiers.org/hco/14/GRCh38#52553129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45457431-C-A

52553129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45457431-C-G

52553129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45457431-C-T

http://identifiers.org/hco/14/GRCh38#52553163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45457465-C-A

52553163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45457465-C-T

52553180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45457482-T-A

52553180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45457482-T-C

http://identifiers.org/hco/14/GRCh38#52553321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45457605-C-A

52553321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45457605-C-G

52553321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45457605-C-T

52553822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45458075-G-T

52554207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45458462-C-T

52554215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45458470-C-T

52554576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45458846-A-G

52554908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45459209-T-C

52554914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45459215-C-G

52555124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45459409-C-T

52555198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45459489-G-A

52555230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45459524-A-G

52555767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45460035-T-A

52555811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45460069-G-C

52556688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45461504-T-C

52557042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45461770-G-C

52557390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45462094-A-G

52557705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45462357-C-T

52560412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45463472-G-T

52561009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45464027-A-T

http://identifiers.org/hco/14/GRCh38#52561371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45464418-A-C

http://identifiers.org/hco/14/GRCh38#52563392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45466121-A-C

52563693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45466245-C-T

http://identifiers.org/hco/14/GRCh38#52563840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45466374-A-C

52563840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45466374-A-G

52563841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45466375-A-G

52566333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45468759-G-T

52566457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45468892-T-A

52566457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45468892-T-G

52566594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45469008-C-T

52566836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45469268-G-A

52566836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45469268-G-C

52566891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45469320-C-T

52566981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45469389-T-C

http://identifiers.org/hco/14/GRCh38#52567037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45469444-C-A

52567037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45469444-C-T

52567061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45469473-C-G

http://identifiers.org/hco/14/GRCh38#52567113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45469509-A-C

52567171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45469548-G-A

52567482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45469838-T-G

52567584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45469946-C-T

52567585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45469947-G-A

52574768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45470465-T-C

52574871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45470540-T-A

52574928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45470598-A-G

52581586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45473241-T-C

52581897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45473534-A-G

52582329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45473954-A-G

52583443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45474597-G-A

52583443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45474597-G-T

52584029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45475557-A-G

52584029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45475557-A-T

http://identifiers.org/hco/14/GRCh38#52584093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45475615-C-A

52585175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45475977-A-G

http://identifiers.org/hco/14/GRCh38#52586598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45476786-A-C

http://identifiers.org/hco/14/GRCh38#52586627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45476812-A-C

52586711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45476889-G-A

52587008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45477538-A-G

52587304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45477831-C-G

52588864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45479390-G-A

52589026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45479675-C-T

http://identifiers.org/hco/14/GRCh38#52589038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45479687-A-C

52589385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45480003-C-T

52589423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45480162-C-T

52597152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45480473-C-G

52597598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45481052-C-T

52597676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45481117-C-T

52598198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45481539-A-G

52598347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45481687-A-G

52598351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45481691-G-A

52598351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45481691-G-T

52598358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45481698-A-G

52598426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45481909-G-A

52598426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45481909-G-C

52598426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45481909-G-T

52598432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45481915-G-T

52598519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45481999-A-G

52598573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45482094-C-G

52598615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45482151-C-T

http://identifiers.org/hco/14/GRCh38#52598694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45482216-A-C

52598698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45482220-G-A

52599159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45482690-T-G

52599347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45482768-C-T

52599795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45482872-A-G

52599851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45482928-A-G

http://identifiers.org/hco/14/GRCh38#52599964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45483587-C-A

52599964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45483587-C-T

52599968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45483591-T-A

52599968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45483591-T-G

52600016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45483665-T-G

52600163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45483795-T-C

52600273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45483905-A-G

52600287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45483919-T-C

http://identifiers.org/hco/14/GRCh38#52600347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45483979-A-C

http://identifiers.org/hco/14/GRCh38#52600400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45484030-A-C

52600400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45484030-A-G

52600416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45484046-A-G

52600908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45484834-T-G

52601199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45485150-A-G

52602162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45485353-A-G

52602186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45485380-G-A

52602186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45485380-G-C

52602336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45485479-T-C

52602336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45485479-T-G

52602729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45485820-A-G

52611698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45485999-A-T

52611700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45486001-T-C

http://identifiers.org/hco/14/GRCh38#52611712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45486010-A-C

52611712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45486010-A-G

52611712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45486010-A-T

52611885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45486134-A-T

http://identifiers.org/hco/14/GRCh38#52611980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45486223-C-A

52611990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45486233-C-G

52612292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45486596-T-A

52612292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45486596-T-C

52612471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45486731-G-A

52612501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45486761-A-G

52615914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45487279-A-T

52616034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45487454-T-G

http://identifiers.org/hco/14/GRCh38#52616105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45487519-A-C

http://identifiers.org/hco/14/GRCh38#52616182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45487819-A-C

52616182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45487819-A-G

52616703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45487997-T-C

52616763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45488049-G-A

52617069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45488718-T-C

52617131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45488794-A-G

52617141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45488804-G-A

52617215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45488859-A-T

52617269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45488907-A-G

52617352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45488998-A-G

52618149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45491733-A-T

52627838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45509288-G-A

52628250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45509700-A-G

52628895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45510240-C-T

52628946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45510291-A-G

52629664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45510989-G-A

52629720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45511037-A-G

52630441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45512016-A-T

52630499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45512074-T-G

52630511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45512080-T-G

52630568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45512152-G-A

http://identifiers.org/hco/14/GRCh38#52630630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45512212-C-A

52630675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45512260-G-A

52630741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45512500-T-A

52630834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45512591-G-A

52630946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45512698-G-A

52631024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45512758-A-G

52631251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45513914-T-G

52631380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45514040-G-C

52631380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45514040-G-T

http://identifiers.org/hco/14/GRCh38#52631758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45514439-C-A

http://identifiers.org/hco/14/GRCh38#52631931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45514616-C-A

52632021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45514701-A-G

52632045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45514725-G-A

52632090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45514770-G-A

52632094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45514774-G-A

52632168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45514850-T-C

52632216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45514898-T-C

http://identifiers.org/hco/14/GRCh38#52632338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45515020-A-C

52632338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45515020-A-G

52632951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45515577-G-A

52633275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45515893-C-T

52633433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45516051-A-G

52633474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45516055-G-A

52633474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45516055-G-T

http://identifiers.org/hco/14/GRCh38#52633489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45516070-A-C

52633489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45516070-A-G

52633773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45516354-C-T

52633953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45516514-G-A

52633953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45516514-G-T

http://identifiers.org/hco/14/GRCh38#52634009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45516562-A-C

52634009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45516562-A-G

http://identifiers.org/hco/14/GRCh38#52634087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45516639-A-C

52634087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45516639-A-G

52634088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45516640-G-A

52634358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45516897-C-T

52634641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45517091-C-G

52634728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45517170-T-G

52634825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45517257-G-A

52634880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45517304-G-A

52634897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45517316-G-A

52635004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45517426-A-G

52635128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45517550-G-A

http://identifiers.org/hco/14/GRCh38#52635200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45517625-C-A

http://identifiers.org/hco/14/GRCh38#52635361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45517755-A-C

52635368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45517762-G-C

52635368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45517762-G-T

52635373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45517767-T-C

52635373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45517767-T-G

http://identifiers.org/hco/14/GRCh38#52635441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45517848-C-A

52635445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45517852-T-G

http://identifiers.org/hco/14/GRCh38#52635519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45517919-C-A

52635519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45517919-C-T

52635638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45518036-A-G

http://identifiers.org/hco/14/GRCh38#52635712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45518114-C-A

52635904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45518300-T-C

52635974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45518370-A-G

52636390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45518818-A-G

http://identifiers.org/hco/14/GRCh38#52636415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45518839-A-C

52636422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45518845-G-T

http://identifiers.org/hco/14/GRCh38#52636427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45518850-C-A

52636450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45518872-A-G

http://identifiers.org/hco/14/GRCh38#52636467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45518896-C-A

http://identifiers.org/hco/14/GRCh38#52636477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45518906-C-A

52636674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45519080-G-A

http://identifiers.org/hco/14/GRCh38#52636706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45519109-A-C

52637106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45519462-G-A

52637106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45519462-G-T

52637288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45519788-T-C

52637543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45520034-G-T

52637558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45520051-G-A

52637558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25445
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45520051-G-T