48564218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 108813792-G-A

48564246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 108813764-G-A

48564246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 108813764-G-T

http://identifiers.org/hco/3/GRCh38#48564260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#108813745-C-A

48564260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 108813745-C-T

http://identifiers.org/hco/3/GRCh38#48564305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#108813685-A-C

48564305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 108813685-A-T

http://identifiers.org/hco/3/GRCh38#48564408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, stop_lost
orthologous variants: http://identifiers.org/mco/9/GRCm39#108813582-A-C

48564425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 108813565-G-A

48564460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108813532-G-A

48564460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108813532-G-C

48564632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108813379-T-C

48565255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108812800-G-A

48565255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108812800-G-T

48565352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108812719-A-G

48565379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108812692-A-G

48565379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108812692-A-T

48565523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108812559-G-T

48565559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108812525-C-G

48565559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108812525-C-T

48565646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108812422-T-C

http://identifiers.org/hco/3/GRCh38#48565720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108812331-A-C

48565720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108812331-A-G

48565739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108812312-G-A

48565739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108812312-G-C

48565998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108812043-G-A

48566087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 108811960-G-A

http://identifiers.org/hco/3/GRCh38#48566134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#108811927-C-A

48566134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 108811927-C-G

48566134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 108811927-C-T

48566148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 108811908-T-C

http://identifiers.org/hco/3/GRCh38#48566157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108811892-A-C

48566157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108811892-A-G

http://identifiers.org/hco/3/GRCh38#48566182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#108811881-C-A

http://identifiers.org/hco/3/GRCh38#48566227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108811833-C-A

48566227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108811833-C-T

48566251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108811803-G-C

48566251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108811803-G-T

48566426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108811630-T-A

48566430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108811626-G-T

48566433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108811623-G-T

48566461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108811607-C-T

48566514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108811585-A-T

48566565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 108811534-T-G

48566566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 108811533-A-G

48566566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 108811533-A-T

48566664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108811439-T-A

48566797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108811305-G-A

48566810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108811292-A-T

48566882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108810435-A-G

48566989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108810328-C-G

48566989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108810328-C-T

48567026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 108810291-G-A

48567036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108810281-A-G

48567091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108810225-C-T

48567096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108810220-C-T

48567263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108810060-T-A

48567263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108810060-T-G

48567320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108810009-A-G

http://identifiers.org/hco/3/GRCh38#48567337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108809993-C-A

48567337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108809993-C-T

http://identifiers.org/hco/3/GRCh38#48567393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108809935-C-A

48567412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108809917-G-T

48567449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108809875-C-T

48567488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108809854-T-A

48567488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108809854-T-C

48567502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108809845-C-T

48567549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108809809-T-C

48567581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108809777-C-T

48567660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108809696-T-C

http://identifiers.org/hco/3/GRCh38#48567820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108809520-C-A

48567820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108809520-C-G

48567824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108809466-C-T

48567828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108809462-C-T

48567854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108809310-C-G

http://identifiers.org/hco/3/GRCh38#48567936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108809217-C-A

48567936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108809217-C-T

48568198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_lost
orthologous variants: 108808837-C-G

48568205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108808830-G-C

48568229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108808806-C-T

48568347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108808718-C-T

48568357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108808708-G-A

48568357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108808708-G-T

48568539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 108808556-G-A

48568559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108808536-C-T

http://identifiers.org/hco/3/GRCh38#48568644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108808460-C-A

48568769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108808366-T-A

48568769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108808366-T-C

48568839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108808296-G-T

48568865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108808270-T-C

48569093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108808242-C-T

48569315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108808041-G-A

48569315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108808041-G-T

48569318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108808033-G-A

48569318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108808033-G-T

48569424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 108807909-A-T

48569523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108807812-C-T

48569578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108807756-G-A

48569677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108807649-T-G

48569787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108807537-G-A

http://identifiers.org/hco/3/GRCh38#48569840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108807493-C-A

48569840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108807493-C-T

48569995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108807347-A-G

48570021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108807315-G-T

48570277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 108807076-G-A

48570277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 108807076-G-T

48570291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108807062-C-T

48570294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108807059-C-T

48570310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108807043-C-T

48570315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108807038-A-G

48570516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108806871-A-T

48570640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 108806779-A-G

48570742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108806679-A-G

48570762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108806659-A-G

48570776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108806648-C-T

48570841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108806559-T-A

http://identifiers.org/hco/3/GRCh38#48570886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108806513-C-A

48570886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 108806513-C-T

48570937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108806462-G-A

48571053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108806350-G-A

48571120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108806305-G-C

http://identifiers.org/hco/3/GRCh38#48571202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108806223-A-C

48571472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805782-C-T

http://identifiers.org/hco/3/GRCh38#48571549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108805702-C-A

48571549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805702-C-T

48571560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805691-G-T

http://identifiers.org/hco/3/GRCh38#48571562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108805689-C-A

48571562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805689-C-G

48571562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805689-C-T

48571580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805686-G-T

http://identifiers.org/hco/3/GRCh38#48571623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108805656-C-A

48571623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805656-C-G

48571623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805656-C-T

48571626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805653-G-A

48571626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805653-G-C

48571626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805653-G-T

48571638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805641-G-A

http://identifiers.org/hco/3/GRCh38#48571639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108805640-C-A

48571639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805640-C-T

48571656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805622-G-T

48571677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805604-G-A

48571677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805604-G-T

48571701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805580-T-C

48571701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805580-T-G

48571757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805520-G-A

48571757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805520-G-T

48571786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805489-A-G

48571786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805489-A-T

48571811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805464-G-A

48571811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805464-G-C

48571811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805464-G-T

48571912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805360-A-G

48571982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108805300-G-A

http://identifiers.org/hco/3/GRCh38#48571989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108805293-C-A

48572012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108805270-G-A

48572019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108805263-G-A

48572020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108805262-G-A

48572021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108805261-G-A

48572021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108805261-G-T

48572067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108805215-G-A

48572071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108805204-G-T

48572101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108805173-C-T

48572259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108805017-G-T

48572280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108804996-G-A

48572400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108804913-C-T

48572507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108804820-T-C

48572510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108804817-C-T

48572580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108804746-C-T

http://identifiers.org/hco/3/GRCh38#48572596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108804724-A-C

48572596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108804724-A-G

48572596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108804724-A-T

http://identifiers.org/hco/3/GRCh38#48572601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108804719-A-C

48572601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108804719-A-T

48572678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108804660-G-A

48572678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108804660-G-T

48572881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108804453-C-G

48572881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108804453-C-T

http://identifiers.org/hco/3/GRCh38#48572905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108804429-C-A

48572905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108804429-C-G

48572905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108804429-C-T

http://identifiers.org/hco/3/GRCh38#48573149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108804173-A-C

48573175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 108804156-A-G

48573202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108804129-G-A

48573296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108804041-C-T

48573576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108803810-G-A

48573778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108803598-G-A

48573804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108803572-G-A

48573877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108803500-G-A

48573965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108803412-C-T

48574160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108803296-G-A

48574160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108803296-G-T

48574183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108803257-A-G

48574324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108803112-A-G

http://identifiers.org/hco/3/GRCh38#48574657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108802779-A-C

48574879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108802561-G-A

48574883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108802557-C-G

48574883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108802557-C-T

48575208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 108802292-T-C

48575208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 108802292-T-G

http://identifiers.org/hco/3/GRCh38#48575302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108802201-C-A

48575400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 108802104-C-T

48575508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108801996-A-T

48575542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 108801962-G-A

48575687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108801817-A-G

48575687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108801817-A-T

48575688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108801816-C-T

48575756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 108801749-A-T

48575799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108801701-A-G

48575799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108801701-A-T

http://identifiers.org/hco/3/GRCh38#48575810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108801684-C-A

48575810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108801684-C-T

48575906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 108801589-G-A

48575945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108801550-G-A

48575945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108801550-G-T

48575992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108801503-C-G

48575998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108801497-C-T

48576035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108801486-T-C

48576098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108801440-T-C

48576119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108801419-C-T

48576124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108801415-T-A

48576124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108801415-T-C

48576391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108801149-G-A

48576391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108801149-G-C

48576455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108801086-G-C

48576866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108800679-G-C

48576922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 108800622-A-G

48576930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108800614-C-T

48576944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108800601-G-T

48577008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108800538-C-T

48577020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108800526-G-C

48577212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108800351-T-C

48577281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108800289-C-T

48577363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108800214-G-A

48577680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108799959-G-A

48578290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108799642-G-A

48578290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108799642-G-C

48578437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108799498-G-C

48578548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108799386-C-T

http://identifiers.org/hco/3/GRCh38#48578591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108799340-C-A

48578768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108799198-A-G

48578768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108799198-A-T

48579048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108798918-A-G

http://identifiers.org/hco/3/GRCh38#48579079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108798886-C-A

48579079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108798886-C-G

48579079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108798886-C-T

48579084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108798881-G-T

48579305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108798697-A-G

http://identifiers.org/hco/3/GRCh38#48579554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108798450-C-A

48579688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108798308-G-A

48579688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108798308-G-T

48579763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108798230-C-T

48579855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108798131-G-A

48579864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108798122-A-G

http://identifiers.org/hco/3/GRCh38#48580034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108797966-C-A

48580034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108797966-C-G

48580053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108797947-G-T

48580141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108797866-C-T

http://identifiers.org/hco/3/GRCh38#48580177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108797830-C-A

48580177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108797830-C-T

48580179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108797828-G-A

48580183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108797805-T-C

http://identifiers.org/hco/3/GRCh38#48580217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108797770-A-C

48580217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108797770-A-G

48580230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108797757-G-T

48580386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108797624-A-T

48580395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108797615-G-C

48580479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108797531-G-T

48580588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108797434-C-T

48580805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108797208-T-C

48581008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108796991-A-T

48581090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108796907-G-A

48581124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 108796870-G-A

48581124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 108796870-G-C

http://identifiers.org/hco/3/GRCh38#48581323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108796688-A-C

48581367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108796643-T-C

48581500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108796507-G-A

48581500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108796507-G-C

48581500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108796507-G-T

48581519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108796490-G-A

48581601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108796402-G-A

48581692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108796305-T-A

48581724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108796273-G-A

48582059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795959-G-T

48582091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795941-G-A

48582091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795941-G-T

http://identifiers.org/hco/3/GRCh38#48582138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108795836-C-A

48582138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795836-C-T

48582139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795835-G-A

48582394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795602-G-A

48582394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795602-G-T

48582457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795553-C-T

48582519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 108795496-T-A

48582520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 108795495-G-A

48582524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795491-A-G

48582643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108795379-C-G

48582693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795332-G-A

48582693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795332-G-T

48582695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795330-C-G

48582695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795330-C-T

48582697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795328-G-A

48582697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795328-G-T

48582726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795324-G-A

48582726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795324-G-T

48582728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795322-G-C

48582729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795321-G-A

http://identifiers.org/hco/3/GRCh38#48582766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108795285-A-C

48582881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795189-T-C

http://identifiers.org/hco/3/GRCh38#48582886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108795180-C-A

48582886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795180-C-G

48582886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795180-C-T

48582894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795172-A-G

48582899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108795167-T-C

48583023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108795018-G-A

48583023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108795018-G-T

48583073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108794968-C-G

48583111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108794937-C-G

http://identifiers.org/hco/3/GRCh38#48583359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108794721-C-A

48583403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108794670-A-G

48583421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108794652-C-G

48583421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108794652-C-T

48583477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108794599-G-A

48583701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108794445-C-G

48583701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108794445-C-T

48583740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108794407-G-A

48583740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108794407-G-T

48583810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108794337-A-G

48583943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108794234-C-T

48584023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108794154-T-C

48584229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108793813-G-A

48584347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108793681-C-T

48584368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108793660-G-A

http://identifiers.org/hco/3/GRCh38#48584448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108793588-A-C

48584585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108793456-T-C

48584681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108793370-A-G

http://identifiers.org/hco/3/GRCh38#48584790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108793266-A-C

48584790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108793266-A-T

48584806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108793249-T-A

48584806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108793249-T-C

48584828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108793217-A-T

http://identifiers.org/hco/3/GRCh38#48584840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108793203-C-A

48584840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108793203-C-T

48584875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108793182-G-A

http://identifiers.org/hco/3/GRCh38#48584931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108793130-C-A

http://identifiers.org/hco/3/GRCh38#48584935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108793126-C-A

48584937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108793124-T-G

48584981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108793082-C-T

48585236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108792837-G-C

48585236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108792837-G-T

48585238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108792835-G-A

48585238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108792835-G-T

48585240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108792833-T-A

48585255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108792819-G-C

48585440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108792468-G-A

48585440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108792468-G-T

48585470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108792444-A-G

48585475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108792439-T-C

48585570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108792333-G-A

48585674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108792230-T-A

48585674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108792230-T-C

http://identifiers.org/hco/3/GRCh38#48585689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108792214-C-A

48585689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 108792214-C-T

http://identifiers.org/hco/3/GRCh38#48585769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108792134-A-C

http://identifiers.org/hco/3/GRCh38#48585770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108792133-C-A

48585770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108792133-C-G

48585770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108792133-C-T

48585818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108792089-A-G

48585861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 108792046-G-A

48585861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 108792046-G-T

48585869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108792038-A-T

48585914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108791993-T-C

48585962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108791944-G-A

http://identifiers.org/hco/3/GRCh38#48586249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108791663-A-C

48586249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 108791663-A-G

48586257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108791655-G-A

48586278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108791633-C-G

48586278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108791633-C-T

http://identifiers.org/hco/3/GRCh38#48586315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108791596-A-C

48586315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108791596-A-G

48586319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108791592-G-C

48586343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108791567-G-A

48586343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108791567-G-C

48586402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108791508-C-T

48586403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108791507-A-G

48586528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108791384-T-C

48586709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108791204-A-G

48586709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108791204-A-T

48586727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108791188-C-T

48586864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108791091-G-A

48586864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108791091-G-T

48586886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108791070-T-C

48586897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108791059-G-A

48586939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108791016-G-A

48586939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108791016-G-T

48586973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 108790981-T-C

48586973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 108790981-T-G

48587090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108790864-G-A

48587090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108790864-G-T

48587138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108790817-G-A

48587138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108790817-G-C

48587138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108790817-G-T

48587512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108790454-G-A

48587512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108790454-G-T

http://identifiers.org/hco/3/GRCh38#48587852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108790105-C-A

48587865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 108790092-G-A

48587953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108790004-G-A

48587953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108790004-G-T

48588003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108789955-G-C

http://identifiers.org/hco/3/GRCh38#48588042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108789915-C-A

48588042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108789915-C-T

48588057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108789888-T-G

http://identifiers.org/hco/3/GRCh38#48588064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108789881-C-A

48588071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108789874-G-C

48588071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108789874-G-T

48588185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108789780-A-G

http://identifiers.org/hco/3/GRCh38#48588293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108789691-C-A

48588293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 108789691-C-T

48588338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108789646-A-G

http://identifiers.org/hco/3/GRCh38#48588356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108789628-C-A

48588391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108789593-C-T

48588420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108789564-A-G

http://identifiers.org/hco/3/GRCh38#48588513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108789510-C-A

48588513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108789510-C-T

http://identifiers.org/hco/3/GRCh38#48588520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108789505-C-A

http://identifiers.org/hco/3/GRCh38#48588686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108789333-A-C

48588791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 108789228-G-A

http://identifiers.org/hco/3/GRCh38#48588810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108789209-A-C

48588826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108789171-C-T

48588827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108789170-A-G

48589185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108788814-G-T

48589194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108788805-T-C

48589202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108788797-G-C

48589202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108788797-G-T

48589214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108788786-G-C

48589214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108788786-G-T

http://identifiers.org/hco/3/GRCh38#48589371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108788656-A-C

48589371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108788656-A-G

http://identifiers.org/hco/3/GRCh38#48589391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108788636-C-A

48589391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108788636-C-T

48589504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108788522-G-A

48590064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787898-G-A

48590064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787898-G-T

http://identifiers.org/hco/3/GRCh38#48590077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108787890-C-A

48590077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787890-C-T

48590130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787853-G-T

48590239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108787746-G-A

48590373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787612-A-T

48590374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787611-T-C

48590418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787556-A-G

48590418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787556-A-T

48590437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787537-C-G

48590437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787537-C-T

http://identifiers.org/hco/3/GRCh38#48590447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108787527-C-A

48590447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787527-C-G

48590581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108787393-G-A

http://identifiers.org/hco/3/GRCh38#48590639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108787335-C-A

48590655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787319-G-C

48590735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108787239-A-G

http://identifiers.org/hco/3/GRCh38#48590798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108787176-A-C

48590837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787139-G-C

48590837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787139-G-T

http://identifiers.org/hco/3/GRCh38#48590853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108787121-A-C

48590869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787105-G-A

48590896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787070-G-A

48590896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787070-G-T

48590924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787042-G-A

48590924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787042-G-T

48590933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787036-T-C

48590933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108787036-T-G

48591040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108786928-G-A

48591040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108786928-G-C

48591323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108786526-T-C

48591571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108786301-G-A

48591571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108786301-G-C

48591613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108786260-G-C

48591812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108786063-T-G

48591818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108786057-C-T

48591831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 108786044-T-C

48591831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 108786044-T-G

http://identifiers.org/hco/3/GRCh38#48591871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108786004-C-A

48591871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108786004-C-T

http://identifiers.org/hco/3/GRCh38#48592021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108785853-A-C

48592021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 108785853-A-G

http://identifiers.org/hco/3/GRCh38#48592140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108785735-C-A

48592140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108785735-C-T

48592397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108785498-A-G

48592422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108785473-T-G

48592487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108785409-G-A

48592487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108785409-G-C

48592619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108785276-G-A

48592666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108785229-G-A

48592768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 108785129-A-T

48592993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108784940-T-C

48593047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108784892-T-C

48593047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108784892-T-G

48593048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108784891-G-T

48593071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108784887-G-A

48593479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108784480-T-C

48593560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108784397-G-A

48593560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108784397-G-T

48593580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108784377-T-C

http://identifiers.org/hco/3/GRCh38#48593619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108784338-C-A

48593619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108784338-C-G

http://identifiers.org/hco/3/GRCh38#48593660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108784297-A-C

48593742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108784208-T-C

48593744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108784206-T-C

48593751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108784199-G-A

http://identifiers.org/hco/3/GRCh38#48593764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108784184-C-A

48593805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108784155-G-T

48594244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108783662-T-C

48594323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108783614-T-G

48594391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108783553-T-C

48594491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108783453-G-A

48594524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 108783420-G-C

48594524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 108783420-G-T

http://identifiers.org/hco/3/GRCh38#48594594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#108783347-A-C

48594611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108783330-G-A

48594820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108783120-C-T

http://identifiers.org/hco/3/GRCh38#48594956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108783000-C-A

48594956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108783000-C-T

48595029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108782929-G-A

48595029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108782929-G-T

48595037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108782921-G-A

48595037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108782921-G-T

http://identifiers.org/hco/3/GRCh38#48595038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108782920-C-A

48595038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108782920-C-T

48595041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108782917-T-C

48595102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 108782871-G-A

48595102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108782871-G-T

48595112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108782861-T-A

48595112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108782861-T-C

http://identifiers.org/hco/3/GRCh38#48595123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108782847-C-A

48595123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108782847-C-T

48595165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 108782805-G-A

48595165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 108782805-G-T

http://identifiers.org/hco/3/GRCh38#48595207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108782762-C-A

48595207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108782762-C-G

48595233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108782736-G-A

48595233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108782736-G-T

http://identifiers.org/hco/3/GRCh38#48595237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108782732-A-C

48595237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108782732-A-G

48595314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2214
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108782654-A-G