42158805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120147013-G-T

42158887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120147093-A-T

http://identifiers.org/hco/15/GRCh38#42158903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#120147109-C-A

42158903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120147109-C-T

42159034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120147241-A-G

http://identifiers.org/hco/15/GRCh38#42159044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120147251-C-A

42159044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120147251-C-T

http://identifiers.org/hco/15/GRCh38#42159517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120147420-C-A

42159517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120147420-C-T

http://identifiers.org/hco/15/GRCh38#42159605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120147469-C-A

42159605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120147469-C-T

42159606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120147470-A-G

42159607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120147471-G-T

42159730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120147587-G-T

42159879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120147733-G-T

http://identifiers.org/hco/15/GRCh38#42160166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120147955-C-A

42160166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120147955-C-T

http://identifiers.org/hco/15/GRCh38#42160173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120147962-A-C

42160173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120147962-A-G

42160188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120147974-G-A

42160188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120147974-G-T

42160213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120148012-A-G

42160259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120148043-T-C

http://identifiers.org/hco/15/GRCh38#42160279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120148058-C-A

42160342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120148120-A-G

42160354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120148132-G-C

42160354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120148132-G-T

42160367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120148145-G-A

42160379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120148157-T-A

42160379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120148157-T-G

42160382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120148160-T-C

42160382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120148160-T-G

42160454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120148237-G-T

http://identifiers.org/hco/15/GRCh38#42160607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120148386-C-A

42160640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120148419-T-A

42160675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120148438-G-C

42160749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120148510-T-G

http://identifiers.org/hco/15/GRCh38#42160763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, stop_lost, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120148524-A-C

42160763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, stop_lost, synonymous_variant
orthologous variants: 120148524-A-G

http://identifiers.org/hco/15/GRCh38#42160775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120148536-C-A

http://identifiers.org/hco/15/GRCh38#42160946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120148671-C-A

42160959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120148684-G-T

http://identifiers.org/hco/15/GRCh38#42161003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120148732-C-A

http://identifiers.org/hco/15/GRCh38#42161015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120148744-C-A

42161015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120148744-C-G

42161015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120148744-C-T

42161043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120148793-A-G

42161258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120149005-G-A

42161258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120149005-G-T

http://identifiers.org/hco/15/GRCh38#42161271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120149018-A-C

42161330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120149073-T-C

42161402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120149218-G-T

http://identifiers.org/hco/15/GRCh38#42161408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120149224-C-A

http://identifiers.org/hco/15/GRCh38#42161426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120149278-C-A

42161517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120149349-G-T

42161753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120150018-T-G

http://identifiers.org/hco/15/GRCh38#42162002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120151104-C-A

42162002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120151104-C-T

http://identifiers.org/hco/15/GRCh38#42162003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120151105-A-C

http://identifiers.org/hco/15/GRCh38#42162289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120151329-C-A

42162289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120151329-C-T

42162498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120151538-T-C

42162530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120151567-G-T

42162559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120151597-T-G

42162565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120151639-G-A

42162565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120151639-G-T

42162569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120151643-T-C

42162623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120151694-T-C

42162656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120151731-G-A

42162656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120151731-G-T

http://identifiers.org/hco/15/GRCh38#42162714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120151771-C-A

42162714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120151771-C-T

42162778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120151832-G-A

42162778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120151832-G-T

42163214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120151961-A-G

42163329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120152069-T-C

42163451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120152170-G-A

42163465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120152184-A-G

http://identifiers.org/hco/15/GRCh38#42163556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120152271-C-A

42163590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120152303-G-T

42163682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120152395-A-G

42164104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120153290-G-T

42164151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120153328-G-T

42164192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120153363-G-A

42164192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120153363-G-C

42164238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120153400-T-C

42164238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120153400-T-G

42164280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120153439-G-A

42164305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120153466-G-A

http://identifiers.org/hco/15/GRCh38#42164312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120153473-C-A

42164520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120153676-A-G

42164597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120153746-G-C

http://identifiers.org/hco/15/GRCh38#42164601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120153750-C-A

42164601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120153750-C-T

42164633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120153781-G-C

http://identifiers.org/hco/15/GRCh38#42164734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120153875-C-A

42164734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120153875-C-T

http://identifiers.org/hco/15/GRCh38#42164927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120153996-C-A

42164927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120153996-C-T

42165012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120154080-G-T

http://identifiers.org/hco/15/GRCh38#42165199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120154241-C-A

42165199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120154241-C-T

42165202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120154244-G-A

42165202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120154244-G-T

42165228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120154270-G-T

42165282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120154309-A-T

http://identifiers.org/hco/15/GRCh38#42165305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120154335-C-A

42165305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120154335-C-T

42165565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120154512-T-C

42165573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120154521-T-G

42165663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120154618-G-A

42165663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120154618-G-T

http://identifiers.org/hco/15/GRCh38#42165668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120154623-C-A

42165668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120154623-C-T

42165680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120154635-G-A

42165680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120154635-G-T

42165908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120154856-T-A

42165912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120154860-G-A

42165912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120154860-G-T

42166273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120155228-C-G

42166273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120155228-C-T

http://identifiers.org/hco/15/GRCh38#42166369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120155336-C-A

42166445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120155413-A-T

42166504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120155460-G-A

42166504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120155460-G-T

http://identifiers.org/hco/15/GRCh38#42166688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120155792-C-A

42166815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120155910-A-G

42166924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120156041-A-G

http://identifiers.org/hco/15/GRCh38#42167024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120156138-A-C

42167057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120156172-A-G

42167058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120156173-G-T

42167069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120156184-C-T

42167214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120156326-T-C

http://identifiers.org/hco/15/GRCh38#42167249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120156361-C-A

42167249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120156361-C-T

42167306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120156417-G-A

42167306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120156417-G-C

42167367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120156460-T-C

42167570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120156664-G-A

42167570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120156664-G-C

42167592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120156686-T-C

http://identifiers.org/hco/15/GRCh38#42167594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120156688-A-C

42167594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120156688-A-G

42167686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120156766-A-G

42168460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120157429-T-C

42168494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120157463-G-A

42168494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120157463-G-C

42168935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120157534-G-T

42169179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120157944-A-G

42169222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120157989-C-T

42169448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120158528-A-G

42169790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: synonymous variant
orthologous variants: 120159120-T-G

42169882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120159212-A-G

42169885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120159215-T-C

http://identifiers.org/hco/15/GRCh38#42169904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120159234-C-A

42169904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120159234-C-T

http://identifiers.org/hco/15/GRCh38#42169923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120159374-A-C

42169968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120159469-T-A

42169992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120159493-G-A

42169992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120159493-G-T

http://identifiers.org/hco/15/GRCh38#42172167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120162724-C-A

42172324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120162855-G-A

42175644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120165654-A-G

42175803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120165791-G-A

42175813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120165801-G-A

42177444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120168511-G-C

42177633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120168668-T-A

42177633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120168668-T-C

http://identifiers.org/hco/15/GRCh38#42178101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120168817-C-A

42178386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120169125-T-C

42178575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 120169287-G-C

42178726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120169448-A-G

42184499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120169782-A-T

42184656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120169939-T-A

42184831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120170109-G-T

42184958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120170215-C-T

42186516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120171107-G-A

42186673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120171263-T-C

http://identifiers.org/hco/15/GRCh38#42186993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120172064-C-A

42187150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120172293-A-G

42187150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120172293-A-T

http://identifiers.org/hco/15/GRCh38#42187161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120172333-C-A

42187161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120172333-C-T

42187167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120172339-T-A

42187167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120172339-T-C

42187193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120172365-G-A

42187193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120172365-G-T

42187202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120172374-G-A

42187202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120172374-G-T

42187235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120172430-T-C

42187236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120172431-A-G

42187256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120172451-A-T

http://identifiers.org/hco/15/GRCh38#42187440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120172637-C-A

42187440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120172637-C-T

http://identifiers.org/hco/15/GRCh38#42187465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120172662-C-A

42187465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120172662-C-G

http://identifiers.org/hco/15/GRCh38#42187725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120173640-A-C

42187740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120173655-A-G

42187750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120173665-G-A

42187845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120173761-G-A

42187845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120173761-G-C

42187888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120173803-A-G

42187960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120173873-A-T

42188145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174016-A-G

42188446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174283-A-G

42188531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174366-A-G

42188625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174456-G-A

42188809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174484-T-C

42188876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174496-G-A

42189251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174735-T-C

http://identifiers.org/hco/15/GRCh38#42189349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120174832-C-A

42190432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175474-A-T

42191028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120176044-T-C

42191097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120176071-A-G

42191225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120176199-G-A

42191225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron variant
orthologous variants: 120176199-G-T

42191337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120176297-G-T

42191352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120176311-A-G

42191352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120176311-A-T

42191476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120176789-G-T

42191595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120176908-T-C

42191640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120176946-T-C

42191709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177005-C-G

42191718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177016-G-A

http://identifiers.org/hco/15/GRCh38#42191932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120177220-C-A

http://identifiers.org/hco/15/GRCh38#42192001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120177278-C-A

42192001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177278-C-G

42192001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177278-C-T

42192005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177282-G-A

42192105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120177377-C-T

http://identifiers.org/hco/15/GRCh38#42192110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120177382-A-C

42192246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177513-G-T

42199355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180178-C-T

http://identifiers.org/hco/15/GRCh38#42199424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120180243-C-A

42199424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180243-C-T

http://identifiers.org/hco/15/GRCh38#42199479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120180295-A-C

42199479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180295-A-G

42199484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180299-T-C

http://identifiers.org/hco/15/GRCh38#42199493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120180308-A-C

http://identifiers.org/hco/15/GRCh38#42199685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120180430-C-A

42199685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180430-C-T

42199711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180455-G-T

42199713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180457-A-G

42199713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180457-A-T

42199718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180462-G-T

http://identifiers.org/hco/15/GRCh38#42199776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120180515-C-A

42199776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180515-C-T

http://identifiers.org/hco/15/GRCh38#42199801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120180535-A-C

http://identifiers.org/hco/15/GRCh38#42199837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120180566-C-A

42199887-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180631-T-A

42199924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120180673-A-G

42199930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120180679-T-A

42199930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120180679-T-C

http://identifiers.org/hco/15/GRCh38#42206202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120181727-C-A

42206202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181727-C-G

42206202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181727-C-T

http://identifiers.org/hco/15/GRCh38#42206273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120181781-A-C

42206281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181789-G-T

42206378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181883-G-A

42206494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181995-A-G

42206798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120182283-T-C

42207101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120182544-G-A

42207211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120182646-C-T

http://identifiers.org/hco/15/GRCh38#42207341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120182782-C-A

42207341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120182782-C-T

42207718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183104-C-T

http://identifiers.org/hco/15/GRCh38#42207932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120183280-C-A

42207932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183280-C-G

42207932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183280-C-T

http://identifiers.org/hco/15/GRCh38#42208013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#120183349-C-A

42208013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120183349-C-T

http://identifiers.org/hco/15/GRCh38#42208035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#120183362-C-A

http://identifiers.org/hco/15/GRCh38#42208180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#120183492-C-A

42208256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120183556-G-A

42208256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120183556-G-T

http://identifiers.org/hco/15/GRCh38#42208281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120183579-A-C

42208281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120183579-A-G

42208281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120183579-A-T

42208299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20593
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120183597-A-G