56099709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112520598-A-G

56099751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112520551-G-A

56099751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112520551-G-T

56099781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112520524-T-G

http://identifiers.org/hco/5/GRCh38#56099816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112520496-C-A

56099816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112520496-C-G

56099816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112520496-C-T

56099844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112520462-A-G

56099918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112520385-T-C

56099923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112520380-T-A

56099962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112520341-A-G

http://identifiers.org/hco/5/GRCh38#56100062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112520236-C-A

56100174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112520120-G-A

56100448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112519790-G-C

56100448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112519790-G-T

56100758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112519502-C-G

56100821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112519475-C-G

56100828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112519468-C-T

56100829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112519467-G-A

56101386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112518965-T-G

56102404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112517845-G-A

56102404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112517845-G-T

56102440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112517810-G-T

56102445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112517805-G-A

56102445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112517805-G-C

56102445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112517805-G-T

56102471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112517780-T-C

56102654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112517593-A-G

56102654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112517593-A-T

56102843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112515762-G-A

56103023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112515574-T-C

56103529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112514571-T-C

56103929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112514123-A-G

56103934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112514118-T-C

56104671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112513623-A-G

56104708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112513591-C-T

http://identifiers.org/hco/5/GRCh38#56104726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112513573-C-A

56104845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112513452-G-C

56104884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112513417-C-T

56104968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112513341-G-A

56105051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112513239-G-T

56105172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112513172-T-C

http://identifiers.org/hco/5/GRCh38#56105304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112513113-C-A

56105333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112513110-C-T

56106101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112512498-A-G

56106159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112512438-T-A

56106165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112512432-A-G

56106218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112512378-G-T

56107196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112509468-A-G

56107295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112509337-G-C

56107314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112509307-A-G

56107325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112509296-A-G

http://identifiers.org/hco/5/GRCh38#56107428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112509180-C-A

56107428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112509180-C-G

56107428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112509180-C-T

56107436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112509172-G-T

56107562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112509044-C-T

56107693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112508896-C-G

56107694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112508895-A-G

56107786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112508790-A-G

56107802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112508774-T-C

56108335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112507493-G-T

56108581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112507247-T-A

56108581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112507247-T-G

56108655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112507166-G-A

56108655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112507166-G-C

56108724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112507089-G-A

http://identifiers.org/hco/5/GRCh38#56108776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112507019-C-A

56108776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112507019-C-T

56108795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112507000-T-A

56108851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112506882-A-G

56108853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112506880-A-G

56108853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112506880-A-T

56109009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112506600-C-G

56109105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112506429-T-A

56109105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112506429-T-G

56109175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112506348-T-C

56109468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112506092-G-A

56110470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112505423-T-C

56110480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112505413-G-T

56110598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112505326-G-A

56110656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112505268-G-A

56110726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112505216-G-A

56110734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112505208-G-T

56110750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112505186-G-T

56110935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112505043-A-G

56110935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112505043-A-T

56110988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112504995-G-A

56111018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112504966-G-C

56111018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112504966-G-T

56111067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112504911-C-T

56111159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112504839-G-C

http://identifiers.org/hco/5/GRCh38#56111186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112504812-C-A

56111186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112504812-C-T

http://identifiers.org/hco/5/GRCh38#56111646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112504352-C-A

56111646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112504352-C-G

56111646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112504352-C-T

http://identifiers.org/hco/5/GRCh38#56111744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112504254-C-A

56111744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112504254-C-T

56111750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112504248-C-T

56111772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112504226-T-C

56111772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112504226-T-G

http://identifiers.org/hco/5/GRCh38#56111788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112504210-C-A

56111788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 112504210-C-G

56111788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 112504210-C-T

56111843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112504144-C-T

56111845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112504142-G-A

56111845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112504142-G-T

56111891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112504105-T-C

http://identifiers.org/hco/5/GRCh38#56112555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112502570-A-C

56112555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112502570-A-G

56116510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112500207-T-A

56116581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112500135-G-T

56116634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 112500095-G-A

56116634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 112500095-G-T

http://identifiers.org/hco/5/GRCh38#56116773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#112499956-C-A

56116790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 112499939-G-T

56116829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112499900-T-C

56116829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112499900-T-G

56116838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112499893-T-C

56116876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112499872-A-G

56116879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112499869-T-A

56116941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112499809-T-C

56116952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112499778-A-G

http://identifiers.org/hco/5/GRCh38#56117009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112499716-C-A

56117021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112499704-T-C

56117021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112499704-T-G

56117051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112499689-G-T

56117075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112499665-A-T

56117320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112499443-A-T

56117777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112499156-C-T

http://identifiers.org/hco/5/GRCh38#56117816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112499119-C-A

56118172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112499080-C-T

56118190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112499066-T-C

56118683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112498914-G-A

56118775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112498747-A-G

56118899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112498564-A-G

56119004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112498507-A-G

56119658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112497615-A-T

http://identifiers.org/hco/5/GRCh38#56119717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112497567-C-A

56120227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112497410-G-A

56120227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112497410-G-T

56120483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112497174-T-G

56120525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112497132-A-G

56120545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112497112-A-T

56120578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112497079-C-T

http://identifiers.org/hco/5/GRCh38#56121167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112496716-C-A

56121173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112496706-G-A

56121173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112496706-G-T

56121727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112496418-G-A

56121761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112496377-G-C

56122137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112496056-A-G

56122148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112496041-T-G

56122149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112496040-A-G

56122357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112495870-T-C

56123118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112495714-G-A

56123118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112495714-G-C

56123223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112495616-G-A

56123292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112495547-C-T

56123441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112495249-G-A

56123646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112495042-A-G

56123743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112494947-G-A

56123743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112494947-G-C

56123950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112494750-A-G

56124075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112494625-A-T

56124231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112494470-G-A

56124343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112494032-C-T

http://identifiers.org/hco/5/GRCh38#56124832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112493876-C-A

56124917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112493811-T-C

56124929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112493799-A-G

56124929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112493799-A-T

56125015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112493723-A-G

56125034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112493704-A-G

56125075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112493679-T-C

56126240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112493246-T-C

56126268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112493218-T-C

56126392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112493091-C-T

56126457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112493028-G-T

56126531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112492974-T-A

http://identifiers.org/hco/5/GRCh38#56126637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112492889-A-C

56126639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112492887-A-G

56126727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112492809-C-T

56126829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112492714-G-A

56126829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112492714-G-T

56126856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112492692-T-C

56126960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 112492584-G-A

56126983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112492561-T-C

56126987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 112492557-G-A

56126987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112492557-G-T

56126994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112492550-C-G

56126994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112492550-C-T

56127014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 112492530-T-C

56127036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112492508-T-C

56127135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112492410-T-C

56127136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112492409-A-G

56127136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112492409-A-T

56127176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112492370-A-G

56127223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112492323-A-T

56127298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112491832-G-C

56127298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112491832-G-T

56127372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112491760-G-A

56127449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112491691-T-C

56127462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112491678-T-C

56127593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112491538-G-T

56127604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112491519-G-A

56127701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112491341-T-A

56127727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112491318-T-C

56127742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112491303-A-G

56127750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112491295-T-A

56127750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112491295-T-C

56127860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112491211-C-G

56128528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112490589-C-G

56128817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112490311-T-A

56128824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112490304-T-C

56129031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112490126-G-A

56129187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112489972-A-G

56129281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112489876-T-C

56129317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112489843-A-G

56129324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112489836-A-G

56129466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112489696-T-C

56129468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112489694-A-G

http://identifiers.org/hco/5/GRCh38#56129533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112489628-A-C

56129859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112488525-T-C

56129988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112488428-G-C

56142701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112486427-A-G

56142702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112486426-G-T

56142859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112486276-A-G

56143050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112486091-A-G

http://identifiers.org/hco/5/GRCh38#56143111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112486054-C-A

56143579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112485641-T-A

56143643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112485577-T-C

http://identifiers.org/hco/5/GRCh38#56143655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112485535-C-A

56143655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112485535-C-T

56143666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112485526-G-C

56143666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112485526-G-T

56143690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112485502-G-T

56143694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112485500-A-G

56143694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112485500-A-T

56143729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112485466-C-T

http://identifiers.org/hco/5/GRCh38#56143730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112485465-C-A

56143730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112485465-C-T

http://identifiers.org/hco/5/GRCh38#56143770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112485425-C-A

56143770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112485425-C-T

56143956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112485239-G-A

56143956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112485239-G-T

56143968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112485228-G-A

http://identifiers.org/hco/5/GRCh38#56143970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112485226-C-A

56144025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112485185-C-T

56144056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112485166-T-C

56144227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112484994-A-G

56144296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112484948-T-A

56144320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112484923-T-C

http://identifiers.org/hco/5/GRCh38#56144412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112484832-C-A

56144541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112484710-G-A

56144541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112484710-G-C

56144604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112484658-A-G

56144769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112484504-G-A

56144864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112484411-G-A

56145258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112484055-T-G

56145348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112483968-A-G

56145772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112483617-G-A

56145891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112483491-T-C

56146880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112482360-G-T

56146907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112482335-A-G

56146947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112482295-A-G

56146947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112482295-A-T

http://identifiers.org/hco/5/GRCh38#56146993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112482248-C-A

56147141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112481936-T-C

56147148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112481929-T-C

56147192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112481885-G-A

56147192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112481885-G-C

56147286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112481788-T-C

http://identifiers.org/hco/5/GRCh38#56147658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112481138-C-A

56147724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112481078-T-C

56147916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112480913-G-A

56148336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112480542-C-T

56148354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112480524-C-T

http://identifiers.org/hco/5/GRCh38#56148367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112480512-C-A

http://identifiers.org/hco/5/GRCh38#56148612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#112480309-A-C

56148648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112480275-C-G

56148687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112480235-C-T

56148804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112480137-C-T

56148848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112480118-T-G

56149312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112479227-G-A

http://identifiers.org/hco/5/GRCh38#56149448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112479106-C-A

56149448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112479106-C-T

56149597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112478950-A-G

56149661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112478838-A-G

http://identifiers.org/hco/5/GRCh38#56149834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112478600-C-A

56151916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112477404-C-T

56151937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112477383-A-G

http://identifiers.org/hco/5/GRCh38#56151971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112477352-C-A

56151971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112477352-C-T

56152055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112477281-T-G

56152142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112477199-T-G

56152178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112477163-G-T

56152447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112476889-T-C

56152604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112476719-A-T

56152724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112476616-A-T

http://identifiers.org/hco/5/GRCh38#56152961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112476387-A-C

56153015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112476350-A-G

56153149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112476216-G-T

56156460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112474052-G-T

56156679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112473865-G-A

56156703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112473856-C-G

56156770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112473790-G-A

56156842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112473720-A-G

http://identifiers.org/hco/5/GRCh38#56156882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112473629-C-A

56156882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112473629-C-G

56158306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112473488-A-G

56158384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112473394-G-A

56158417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112473358-T-C

56158449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112473327-T-C

56158566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112473210-G-A

56159624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112472947-T-C

56159633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112472938-G-A

56159745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112472876-T-G

56159753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112472868-G-A

56159753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112472868-G-T

http://identifiers.org/hco/5/GRCh38#56159788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112472845-C-A

56159788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112472845-C-T

56159878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112472762-C-T

56159941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112472703-G-A

56159941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112472703-G-C

56159941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112472703-G-T

http://identifiers.org/hco/5/GRCh38#56159983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112472672-C-A

56159983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112472672-C-G

56159983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112472672-C-T

http://identifiers.org/hco/5/GRCh38#56159999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112472651-C-A

56160086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112472583-T-G

56160883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112472220-C-T

http://identifiers.org/hco/5/GRCh38#56160887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112472216-A-C

56160887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112472216-A-G

56160987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112472128-G-T

56161003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, undefined
orthologous variants: 112472115-C-T

56161031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112472087-A-G

56161159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112471965-A-T

56161175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112471949-G-C

56161177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112471947-C-T

56161292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112471848-G-C

56161363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112471790-A-T

56161440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112471714-C-T

56161538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112471098-G-C

56161630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112471014-A-G

56161832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112470839-T-G

56161945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112470723-C-G

56161945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112470723-C-T

56162072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112470630-G-T

56162118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112470561-G-A

56162118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112470561-G-T

http://identifiers.org/hco/5/GRCh38#56162387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112470123-C-A

56162409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112470110-G-A

56162423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112470096-G-A

56162454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112470070-T-C

56162586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112470032-A-G

56163296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112469364-A-G

56163366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112469300-A-G

56163377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112469289-T-C

56163567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112469105-T-C

http://identifiers.org/hco/5/GRCh38#56164115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112468782-A-C

56164218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112468707-G-C

http://identifiers.org/hco/5/GRCh38#56164314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112468645-C-A

http://identifiers.org/hco/5/GRCh38#56164390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112468564-C-A

56164456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112468508-T-G

56164775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112468192-G-C

56164844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112468145-T-C

56164845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112468144-T-A

56165058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112467972-G-A

56165192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112467834-T-G

56165557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112467465-C-G

56165598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112467422-C-T

56168080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112465004-G-A

56170625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112463828-G-T

56170643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112463810-T-C

56170700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: missense variant
orthologous variants: 112463764-T-C

http://identifiers.org/hco/5/GRCh38#56170766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112463698-C-A

56170766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: missense variant
orthologous variants: 112463698-C-T

56170850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112463619-A-G

56171074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112463226-G-A

56171566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112462612-T-C

56171726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112462457-C-T

56172137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112462112-T-A

56172280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112462052-C-T

56172294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112462040-G-A

56172437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112461896-A-G

56172502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112461822-G-A

http://identifiers.org/hco/5/GRCh38#56172627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112461702-C-A

56172664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112461670-A-G

56172682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112461648-A-G

56174038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112461406-G-A

56174038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112461406-G-C

56174244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112461243-G-A

56174877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112460916-T-C

56174891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112460904-A-G

56175223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112460644-T-C

56175482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112460411-G-T

56175546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112460347-A-G

56175794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112460060-T-G

56175911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112459950-C-T

56176020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112459837-A-G

56176107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron variant
orthologous variants: 112459757-C-T

56176315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112459551-T-C

56176315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112459551-T-G

56176401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112459462-G-T

56176409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112459454-G-T

56176411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112459452-G-A

56176411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112459452-G-T

56176540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112459295-G-C

56176649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112459192-C-T

56176876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112458756-G-C

56177404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112458154-G-A

56183558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112455033-T-C

56183558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112455033-T-G

56183774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112454818-T-C

56183827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112454756-A-T

56183901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112454686-A-G

56183950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112454561-C-T

56184106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112454274-T-C

56184163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112454241-A-G

56184216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112454184-T-G

56184236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112454170-C-T

56184270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112454136-A-G

56185748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112453659-T-A

56186090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112453393-C-T

56186118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112453360-G-A

56186136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112453339-C-T

56188146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112452293-A-G

http://identifiers.org/hco/5/GRCh38#56188875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112451813-A-C

56189013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112451682-T-C

56189157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112451535-G-A

56189353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112451499-A-G

56189353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112451499-A-T

56189616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112451247-G-A

56189733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112451076-C-G

56189738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112451071-G-A

56189745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112451045-T-A

56189811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112450845-T-G

56189944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112450504-C-T

http://identifiers.org/hco/5/GRCh38#56190018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112450429-C-A

56190252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112450166-A-G

56190363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112450087-C-T

56190389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112450061-A-G

http://identifiers.org/hco/5/GRCh38#56190455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112449995-A-C

56190590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112449879-G-A

56191067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112449624-A-G

56191270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112449415-T-C

56191441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112449256-T-C

56191554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112449146-G-A

56191652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112449057-G-A

56191653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112449056-A-G

56200464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112446150-A-G

56200474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112446143-C-T

56200555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112446078-C-G

56200779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112445883-A-G

56201062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112445622-C-T

56201142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112445543-C-T

56201176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112445504-T-C

56201293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112445373-G-C

56201320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112445346-A-G

56204759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112444635-G-T

56204831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112444583-C-T

56204841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112444573-T-G

56204940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112444475-G-A

56204975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112444427-G-A

56205576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112444186-A-G

56205611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112444151-T-G

56205619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112444143-T-C

56205620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112444142-A-G

56206452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112439123-T-A

56206527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112439051-G-T

56206569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112439001-G-C

56206733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112438836-C-T

http://identifiers.org/hco/5/GRCh38#56210611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112437740-C-A

56210617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112437734-C-T

56210685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112437666-T-C

56210718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112437621-G-A

56210835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112437501-G-T

56210890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112437449-G-A

56210890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112437449-G-C

56211106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112437233-C-T

56211334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112437015-A-G

56211335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112437014-T-C

56211584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112436767-T-C

56211664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112436688-G-A

56211779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112436582-T-C

56211897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112436470-G-A

56211944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112436424-A-T

56214273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112435911-G-A

http://identifiers.org/hco/5/GRCh38#56214318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112435885-C-A

56214508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112435631-T-G

56214509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112435620-A-G

56214857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112435055-G-A

56214857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112435055-G-C

56214857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112435055-G-T

56215063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112434834-G-A

56215235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112434696-T-A

http://identifiers.org/hco/5/GRCh38#56215958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112434048-A-C

56215958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112434048-A-G

56215987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112434018-C-T

56216015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112433992-G-A

56216015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112433992-G-T

56218781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112433464-C-T

56218823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112433435-G-A

56218876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112433405-C-T

56219479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112432798-C-T

56219481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112432796-A-G

56219601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112432678-C-T

56219631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112432646-C-G

56219641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112432639-T-C

http://identifiers.org/hco/5/GRCh38#56219906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112432481-A-C

56219963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112432423-T-A

56219985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112432399-A-G

56220043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112432353-G-A

56220078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112432317-T-C

56220230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112432200-A-G

56220231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112432199-C-T

http://identifiers.org/hco/5/GRCh38#56220348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112432066-C-A

56220400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112432015-T-C

56221165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112431693-T-C

56221165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112431693-T-G

56221170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112431688-T-C

56221185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112431679-A-T

56221244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112431634-T-C

56221315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112431562-G-A

56228764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112429714-A-G

56228764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112429714-A-T

56229055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112429431-G-A

56229114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112429411-T-G

56229126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112429399-C-G

56229126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112429399-C-T

http://identifiers.org/hco/5/GRCh38#56229388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112429149-C-A

56229388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112429149-C-T

56229439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112429105-T-A

56229735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112428917-T-C

56229847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112428811-C-T

56229954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112428723-G-A

56230010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112428672-G-A

56230055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112428625-G-A

56230055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112428625-G-C

56230068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112428613-A-G

56230593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112427614-G-T

56230602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112427605-A-G

56230631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112427579-G-T

56230741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112427463-T-C

56230977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112427273-T-C

56231311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112426962-G-A

56231632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112426633-G-A

56231725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112426539-G-C

56232015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112426280-A-G

56232067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112426228-T-C

56232092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112426197-T-C

56232110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112426180-A-G

56232183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112426112-A-G

56232213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112426087-G-T

56232466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112425829-T-C

56232554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112425751-T-C

56232630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112425695-T-C

http://identifiers.org/hco/5/GRCh38#56232731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112425617-C-A

56232731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112425617-C-T

http://identifiers.org/hco/5/GRCh38#56232733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112425615-C-A

56232733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112425615-C-G

56232733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112425615-C-T

56232740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112425608-A-G

56232773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112425575-T-A

56232797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112425550-T-A

56232797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112425550-T-C

http://identifiers.org/hco/5/GRCh38#56233109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112425267-C-A

56233160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112425207-A-G

56233160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112425207-A-T

http://identifiers.org/hco/5/GRCh38#56233184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112425185-C-A