http://identifiers.org/hco/13/GRCh38#99200812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#122116055-C-A

99200812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 122116055-C-G

99200812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 122116055-C-T

99200977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122116223-A-G

http://identifiers.org/hco/13/GRCh38#99200980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122116226-C-A

99200980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122116226-C-T

http://identifiers.org/hco/13/GRCh38#99201053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122116295-C-A

99201053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122116295-C-T

99201098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 122116340-T-C

99201098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 122116340-T-G

99201141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122116383-G-A

http://identifiers.org/hco/13/GRCh38#99201180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#122116414-C-A

99201180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 122116414-C-G

99201180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 122116414-C-T

99201469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122116737-G-A

99201603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122116871-G-A

99201603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122116871-G-C

http://identifiers.org/hco/13/GRCh38#99201668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#122116947-C-A

99201668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122116947-C-G

99201668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122116947-C-T

99201711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122116998-T-C

http://identifiers.org/hco/13/GRCh38#99202466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122117403-A-C

99202466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122117403-A-G

99202475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122117411-T-A

99202512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122117451-T-C

99202950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122118097-G-C

99203022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122118145-A-G

99203027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122118150-A-T

99203070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122118184-C-T

99203110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122118215-C-T

99203112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122118217-C-T

99203172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122118278-G-C

99203546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122118567-C-G

99203642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122118651-G-A

99203776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122118757-A-G

99203780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122118761-G-A

99203780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122118761-G-C

99203976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122118983-G-A

99204432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122119411-T-C

99204708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122119702-C-T

99204724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122119718-C-T

99206477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121083-T-C

99206477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121083-T-G

99206588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121188-T-C

99206887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121632-C-T

99207163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121826-C-T

99209845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122124675-C-T

99210396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122125103-T-C

99213346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122127975-C-T

99213370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122127992-G-T

99213463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122128046-T-C

99213486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122128087-G-T

http://identifiers.org/hco/13/GRCh38#99213795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122128386-A-C

99214135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122129157-G-A

99214291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122129297-G-C

99214358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122129415-T-G

99214377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122129432-T-C

99214568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122129686-T-C

99214568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122129686-T-G

99214612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122129730-C-T

http://identifiers.org/hco/13/GRCh38#99214665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122129782-C-A

99214717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122129828-C-G

99214745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122129833-T-G

99216411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122130529-G-A

99216462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122130579-A-G

99216605-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122130693-T-A

99216737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122130804-G-C

99217342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122131091-C-G

99217342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122131091-C-T

99217419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122131160-C-T

99217434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122131177-G-A

99217435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122131178-T-C

99217569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122131293-A-G

99217581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122131305-C-T

99217631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122131372-G-A

99217664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122131406-C-T

99217714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122131441-G-A

99217714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122131441-G-C

99217714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122131441-G-T

99217764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122131483-T-C

99217764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122131483-T-G

99217806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122131505-G-A

99218168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122131803-A-G

99218508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122132159-C-T

99218536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122132187-G-T

99218888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122132603-C-T

99218935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122132681-G-C

99218935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122132681-G-T

99219027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122132783-T-G

http://identifiers.org/hco/13/GRCh38#99219099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122132820-A-C

99219117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122132838-G-A

99220018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122133269-G-C

99220206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122133461-G-A

99220308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122133559-A-G

99220341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122133592-A-G

99220719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122133887-G-A

99221736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122136324-C-T

99227379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122140003-T-C

99227730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122140333-C-G

99227766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122140369-A-G

http://identifiers.org/hco/13/GRCh38#99227814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122140420-C-A

99227904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122140468-G-C

99228706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122140966-A-G

99228771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122141030-C-T

99228905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122141147-A-G

99228908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122141150-C-T

99228954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122141196-C-T

99228974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122141215-T-G

99229214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122141370-A-G

99229437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122141495-T-C

99229439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122141497-C-T

99229786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122141732-A-G

99229995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122141925-G-T

99230127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122142061-T-G

99235183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122142220-T-C

99238231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122142358-C-T

http://identifiers.org/hco/13/GRCh38#99238323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122142430-C-A

99238368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122142478-T-C

99238595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122142705-G-T

99238923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122143601-G-T

99238973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122143647-G-A

http://identifiers.org/hco/13/GRCh38#99243081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122144023-C-A

99243176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122144099-A-G

99243380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122144256-A-G

99243826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 122144697-A-G

99243826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 122144697-A-T

99243979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122144856-T-C

99244053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122145132-T-C

99244172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122145266-G-A

99244172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122145266-G-C

99244186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122145280-T-A

http://identifiers.org/hco/13/GRCh38#99244222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122145309-A-C

http://identifiers.org/hco/13/GRCh38#99244297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122145400-A-C

99244387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122145489-G-A

99244387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122145489-G-C

99244387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122145489-G-T

99244405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122145508-A-G

99244405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122145508-A-T

99244411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122145514-A-G

99244447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122145566-G-T

http://identifiers.org/hco/13/GRCh38#99244448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122145567-C-A

99245026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122146141-G-T

99246085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122146714-A-G

http://identifiers.org/hco/13/GRCh38#99251623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122147369-A-C

99251709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122147450-G-T

99251717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122147458-C-T

99251724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122147462-C-T

99251730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122147468-T-A

99251819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122147552-A-G

99251837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122147571-C-G

99252012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122147696-C-T

http://identifiers.org/hco/13/GRCh38#99252088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122147811-A-C

99252293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122148016-T-A

http://identifiers.org/hco/13/GRCh38#99252487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122148185-A-C

99252487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122148185-A-G

99254473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122148460-G-A

99254474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122148461-G-T

99254579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122148530-T-A

99254579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122148530-T-C

http://identifiers.org/hco/13/GRCh38#99254600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122148551-C-A

99254600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122148551-C-T

99254644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122148586-G-T

http://identifiers.org/hco/13/GRCh38#99254718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122148878-A-C

99254718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122148878-A-T

99254943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 122149094-C-T

99255030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122149181-C-T

http://identifiers.org/hco/13/GRCh38#99255090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122149241-C-A

99255090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122149241-C-T

99255216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122149367-C-T

99255222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122149373-G-A

99255222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122149373-G-T

99255279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122149430-A-T

99255318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122149469-G-A

99255337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 122149488-A-G

99255366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122149517-G-A

99255366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122149517-G-C

99255450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122149601-C-T

99255567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122149718-C-T

99256157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122150891-T-G

99256175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122150904-A-G

99256297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122150982-T-A

99256517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 122151173-C-T

http://identifiers.org/hco/13/GRCh38#99256551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122151209-C-A

http://identifiers.org/hco/13/GRCh38#99256730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122151532-A-C

99256799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122151596-C-G

99256847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122151639-A-G

99256873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122151667-T-G

99256892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122151686-A-G

99257192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122151928-T-C

99257397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122152208-A-G

99257761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122152517-C-T

http://identifiers.org/hco/13/GRCh38#99258188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#122153122-C-A

http://identifiers.org/hco/13/GRCh38#99258195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#122153129-C-A

99258230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122153163-G-T

99258381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 122153272-C-G

99258514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122153401-T-C

99258657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122153527-T-C

99259158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122153942-G-A

99259600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122154436-A-G

99259740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122154563-C-T

99260299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122154888-C-T

99260749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122155139-G-C

99260915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122155286-A-G

99260925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122155296-A-G

99260978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122155350-C-T

99261507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122156302-T-A

99261792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122156591-T-C

99263178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122157275-T-C

99263608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122157673-C-T

99263696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122157744-C-T

99263881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122157893-A-T

99263944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122157966-A-G

99263948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122157970-C-T

99264088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122158194-C-G

99264245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122158320-C-T

99264453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122158586-C-T

99264593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122158679-G-A

99264626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122158697-G-A

99264850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122158830-G-A

99264975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122158932-T-G

99265007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122158964-T-G

99265078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122159027-C-T

99265428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122159860-T-A

99265428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122159860-T-G

99265578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160008-T-C

99265578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160008-T-G

http://identifiers.org/hco/13/GRCh38#99265636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122160049-C-A

http://identifiers.org/hco/13/GRCh38#99265637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122160050-A-C

99265637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160050-A-T

99265650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160057-A-G

99265997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160352-C-G

99265997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160352-C-T

99266010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160365-C-T

99266140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160493-T-A

99266201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160549-A-T

99266493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160596-A-G

99267093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122163318-T-C

99267185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122163403-T-C

99267435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122163632-G-A

99267621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122163756-T-G

99267651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122163786-G-A

99268737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122164411-G-A

99269300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122165261-G-A

http://identifiers.org/hco/13/GRCh38#99269427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122165381-A-C

99269581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122165511-A-G

99269602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122165532-A-G

http://identifiers.org/hco/13/GRCh38#99269685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122165838-C-A

99269745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122165896-T-C

99269990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122166157-G-A

99270073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122166241-C-T

99270195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122166523-A-G

99270285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122166606-A-T

99270352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122166660-T-G

99270362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122166672-A-G

99270534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122166838-A-T

99270558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122166854-A-T

99270614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122166908-A-T

http://identifiers.org/hco/13/GRCh38#99270802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122167085-A-C

99270803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122167086-A-G

99270803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122167086-A-T

99277915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122171776-G-A

99277915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122171776-G-T

http://identifiers.org/hco/13/GRCh38#99278343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122172110-C-A

99278343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122172110-C-T

99278563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122172301-T-C

99279237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122173818-G-A

99279237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122173818-G-C

99279460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122174031-A-G

99279673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122174254-T-G

99281373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122174981-G-C

99281437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122175042-A-G

99281515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122175109-C-T

http://identifiers.org/hco/13/GRCh38#99281586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122175171-A-C

http://identifiers.org/hco/13/GRCh38#99281597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122175182-A-C

99281700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122175288-A-G

99281782-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122175348-A-T

99281876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122175420-C-T

99282206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122175759-G-A

99283006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122176520-A-T

99283135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122176603-T-C

99286440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122184277-A-G

99286894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122184398-G-A

99286894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122184398-G-T

99287295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122184747-G-T

99288525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122185459-C-T

http://identifiers.org/hco/13/GRCh38#99288627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122185558-C-A

99288693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122185601-T-C

99288963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122185854-G-A

99288963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122185854-G-T

99289049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122185935-A-G

99289119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122186001-A-G

99289119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122186001-A-T

99289126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122186009-T-C

99289255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122186146-A-G

99289772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122186601-T-G

99289876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122186683-T-A

99291357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122187707-T-C

99291373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122187723-G-A

99291373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122187723-G-T

99291441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122187768-G-A

http://identifiers.org/hco/13/GRCh38#99291491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122187821-A-C

http://identifiers.org/hco/13/GRCh38#99292035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122188316-A-C

99292035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122188316-A-G

http://identifiers.org/hco/13/GRCh38#99292240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122188395-A-C

99292650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122188702-T-G

99292664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122188715-C-T

99292768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122188839-G-T

99293365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122189388-G-A

99293374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122189397-C-G

99293374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122189397-C-T

99293438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122189441-G-A

99293623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122189624-G-C

99293897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122190048-T-G

99293989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122190144-A-G

http://identifiers.org/hco/13/GRCh38#99294605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122191052-A-C

99294605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122191052-A-T

99294727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122191184-A-T

99294811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122191258-G-C

99294886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122191314-T-G

99294976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122191385-T-C

99295117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122191503-T-G

http://identifiers.org/hco/13/GRCh38#99295156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122191542-C-A

99295156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122191542-C-T

99295201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122191587-A-G

99295306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122191692-A-G

http://identifiers.org/hco/13/GRCh38#99295328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122191714-C-A

99295328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 122191714-C-T

99295396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122191782-A-G

99295606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122191992-T-C

99295705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122192091-A-G

99295705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 122192091-A-T

99295747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122192133-C-T

99296119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122192505-A-G

99296475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122192762-G-A

99296497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122192782-T-C

http://identifiers.org/hco/13/GRCh38#99296559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122192850-A-C

99296570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122192861-C-G

99296588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122192879-G-C

99296939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122193352-G-A

99297111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122193542-T-C

99298141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122194705-A-G

99298372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122194919-A-G

99299542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122195962-T-C

99300613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122196746-T-A

99300731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122196850-C-T

99300866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122196918-T-C

99300984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122197058-T-C

99301524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122197758-T-C

99306371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122201543-G-A

99306395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122201569-A-T

99306555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122201701-C-G

99306583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122201729-A-G

99306617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122201766-A-G

99306762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122201941-T-C

99307215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122202371-G-A

99307373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122202496-G-A

99307373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122202496-G-T

99307691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122202806-G-A

99307820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122202938-G-A

99307820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122202938-G-T

http://identifiers.org/hco/13/GRCh38#99307855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122202977-C-A

99307911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122203025-A-G

99307985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122203091-G-A

99307985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122203091-G-T

99307998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122203104-A-G

99308073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122203173-A-G

99308234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122203292-G-C

99308360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122203400-T-G

99308651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122203825-A-G

99308720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122203912-G-T

http://identifiers.org/hco/13/GRCh38#99308756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122203950-C-A

99308771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122203965-A-G

99308914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122204084-A-G

99310563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122204886-T-G

99311427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122207661-G-A

99312152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122209567-G-C

99312256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122209655-A-G

99312270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122209682-G-T

99312703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122210173-G-T

http://identifiers.org/hco/13/GRCh38#99312759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122210205-C-A

99312759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122210205-C-T

99313391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122210422-A-G

99313439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122210467-A-T

99313450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122210478-A-G

99313470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122210489-C-T

99313560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122210590-G-C

99313601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122210626-A-G

99313605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122210629-C-G

99313850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122210809-G-A

99313971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122210917-T-C

http://identifiers.org/hco/13/GRCh38#99314224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122211148-C-A

99314224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211148-C-G

99314226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211150-G-C

99314226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211150-G-T

http://identifiers.org/hco/13/GRCh38#99314254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122211177-A-C

99314254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211177-A-G

99314254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211177-A-T

http://identifiers.org/hco/13/GRCh38#99314335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122211273-C-A

99314335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211273-C-T

99314371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211309-G-C

99314371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211309-G-T

99314372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211310-T-A

99314372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211310-T-G

99314405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211343-T-C

99314420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211358-A-G

http://identifiers.org/hco/13/GRCh38#99316540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122212618-A-C

99316540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122212618-A-G

99316763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122212781-G-A

99316943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122212978-G-T

99317168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122219241-G-C

99317168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122219241-G-T

99317252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122219325-C-G

99317252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122219325-C-T

99317570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122220246-A-G

99317827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122220494-A-G

99317891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122220556-G-T

http://identifiers.org/hco/13/GRCh38#99317908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122220573-C-A

99317908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122220573-C-G

99317909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122220574-A-G

99317932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122220596-A-T

99317936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122220600-G-T

99317945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122220605-A-G

99317953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122220614-G-A

99317953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122220614-G-T

99317995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122220655-T-C

99317996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122220656-A-T

99318000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122220660-G-T

99318155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122220833-T-C

99318876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122220946-C-T

http://identifiers.org/hco/13/GRCh38#99318959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122221057-C-A

99319228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122221303-T-C

http://identifiers.org/hco/13/GRCh38#99319483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122221571-C-A

99319706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122221938-A-G

99320180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122222290-A-G

99320468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122222543-C-G

99320622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122222740-G-A

99320625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122222743-A-G

99320751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122222940-A-G

99320861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122223089-C-G

99320953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122223186-T-C

99321006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122223223-T-C

99321298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122223495-T-G

99321610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122223930-G-C

99321610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122223930-G-T

99321773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122224115-A-G

99321872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122224192-G-A

99321934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122224251-T-C

99322405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122224935-T-G

99322713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122225259-G-A

99322713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122225259-G-C

http://identifiers.org/hco/13/GRCh38#99322856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122225398-A-C

99322923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122225464-C-G

99323061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122225581-C-T

99323089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122225609-C-T

99323115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122225624-C-G

99323233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122225742-C-T

99331788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122226438-C-G

99332031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122226674-G-A

99332254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122226911-A-G

99332291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122226948-C-T

99332482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122227278-T-C

99333141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122228135-T-C

99333306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122228315-G-T

99333315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122228324-T-C

99333316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122228325-A-G

99339794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122230963-G-A

99340264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122231591-A-G

99340264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122231591-A-T

99340267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122231594-T-A

99340267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122231594-T-C

99340299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231617-C-G

99340299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231617-C-T

99340300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231618-A-G

99340300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231618-A-T

99340646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231936-T-C

99340646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231936-T-G

http://identifiers.org/hco/13/GRCh38#99340655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122231951-C-A

99340669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231965-G-A

99340669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231965-G-T

99340679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231975-T-A

99340679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231975-T-C

99340923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122232229-A-G

99341175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122232475-C-T

http://identifiers.org/hco/13/GRCh38#99341187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122232488-C-A

99341235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122232532-G-A

99341374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122232665-G-T

99341412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122232691-T-C

http://identifiers.org/hco/13/GRCh38#99342275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122233360-C-A

99342275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122233360-C-T

99342611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122233654-G-A

99342685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122233728-C-T

99342686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122233729-G-A

99342686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122233729-G-C

99342698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122233742-A-G

99348253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122235103-C-T

99350950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122236153-C-G

99351036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122236244-A-G

99351155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122236342-T-A

99351155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122236342-T-C

99351185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122236368-T-A

99351325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122236503-A-G

99351381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122236559-G-A

99351412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122236593-C-T

http://identifiers.org/hco/13/GRCh38#99351542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122236717-C-A

99351621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122236788-G-A

99351673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122236831-C-G

99351796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122236911-T-A

http://identifiers.org/hco/13/GRCh38#99351831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122236938-C-A

http://identifiers.org/hco/13/GRCh38#99351906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122237032-C-A

99351906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122237032-C-G

99351906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122237032-C-T

99351907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122237033-A-T

99351917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122237043-A-G

99351981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122237113-A-G

http://identifiers.org/hco/13/GRCh38#99352023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122237155-C-A

99352023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122237155-C-G

99352097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122237227-A-G

99352245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122237331-G-A

99352470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122237756-G-A

99352497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122237783-A-G

99352619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122237891-G-A

99352691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122237960-A-G

99352698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122237967-G-A

99353129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122238273-T-C

http://identifiers.org/hco/13/GRCh38#99353775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122238865-C-A

99354140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122239171-C-G

99354140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122239171-C-T

99354722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122239786-C-T

99354735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122239798-G-C

99356021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122240208-T-C

99356065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122240252-A-G

99356067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122240254-G-A

99356068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122240255-T-A

99356068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122240255-T-G

99356114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122240302-C-T

99356287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122240461-G-A

99356287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122240461-G-T

http://identifiers.org/hco/13/GRCh38#99356314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122240485-C-A

99356314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122240485-C-G

99356314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122240485-C-T

99356474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122240613-C-T

99356515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122240640-T-C

99356585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122240706-A-G

99356965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122240859-T-C

99357506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122241033-G-A

99357889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122241407-A-G

99358385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122241737-C-T

99358778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122242389-A-G

99358900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122242500-T-C

99367118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122245468-G-A

99367145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122245495-C-T

99367153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122245503-G-A

99367153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122245503-G-T

99367233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122245635-C-G

99367726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122246147-C-T

99367771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122246187-G-A

99367845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122246261-A-G

99367875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122246294-C-T

99368011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122246422-A-T

99370846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

99371042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

99371042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

http://identifiers.org/hco/13/GRCh38#99371099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

99371327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122249177-T-C

99371327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122249177-T-G

99371968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122249480-G-A

99372284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122249678-A-G

99372384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122249744-G-A

99372384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122249744-G-C

99372384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122249744-G-T

http://identifiers.org/hco/13/GRCh38#99372432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122249789-C-A

99372432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122249789-C-G

99372432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122249789-C-T

99372593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122249940-G-A

99372607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122249954-G-A

99372608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122249955-G-A

99372608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122249955-G-T

99372617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122249964-G-A

99372617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122249964-G-T

http://identifiers.org/hco/13/GRCh38#99372637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122249980-A-C

99372671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122250011-G-T

99372677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122250022-G-A

99372677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122250022-G-T

99372678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122250023-G-A

99372678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122250023-G-T

99372701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122250046-G-A

99372701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122250046-G-T

99375375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122250995-G-A

99375732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122251356-A-G

99376046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122251426-G-A

http://identifiers.org/hco/13/GRCh38#99376247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#122251605-C-A

99376859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122252287-G-A

99381370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122253100-A-G

99381836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122253539-A-G

99381862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122253566-A-G

99381862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122253566-A-T

99381947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122253646-A-G

99382042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122253744-G-T

99382253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122253953-A-G

99385387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122257495-G-A

99385387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122257495-G-C

99385387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122257495-G-T

99385600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122257701-G-A

99385600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122257701-G-T

99385713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122257814-G-T

99385841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122257929-T-C

http://identifiers.org/hco/13/GRCh38#99385952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122258017-C-A

99385966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122258031-G-T

99386041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122258112-G-T

99386176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122258201-C-G

99386176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122258201-C-T

http://identifiers.org/hco/13/GRCh38#99386203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#122258227-C-A

99386203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122258227-C-T

99386288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20486
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122258301-A-G