http://identifiers.org/hco/17/GRCh38#79932381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119031453-C-A

79932404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119031476-G-C

http://identifiers.org/hco/17/GRCh38#79932539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119031578-C-A

79932539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119031578-C-T

79932633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119031673-A-G

79932754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119031766-G-T

79932793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119031786-T-C

http://identifiers.org/hco/17/GRCh38#79932817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119031810-C-A

79932919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119031881-T-G

79932937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119031899-G-A

79933243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032217-C-T

79933254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032227-G-A

79933254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032227-G-T

79933265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032238-G-A

79933265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032238-G-T

79933429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032366-A-G

79933455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032395-A-G

79933489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032425-G-A

79933489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032425-G-T

79933526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032449-T-C

http://identifiers.org/hco/17/GRCh38#79933687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119032583-C-A

79934304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032722-T-C

79934316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032735-G-A

79934317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032736-G-C

79934317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032736-G-T

79934325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032744-T-A

79934325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032744-T-C

http://identifiers.org/hco/17/GRCh38#79934335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119032754-C-A

79934360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032779-G-A

79934390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032829-G-A

79934390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032829-G-T

79934403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032850-G-T

http://identifiers.org/hco/17/GRCh38#79934413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119032860-C-A

79934413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032860-C-T

79934417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032864-G-A

79934425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032872-G-C

79934425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032872-G-T

79934463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032903-C-T

79934474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032921-G-T

79934482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032929-G-A

79934482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032929-G-T

79934523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119032968-G-C

79934676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033057-C-T

79934694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033070-G-A

79934701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033077-A-G

79934731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033083-G-A

79934731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033083-G-C

79934731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033083-G-T

79934736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033088-T-C

http://identifiers.org/hco/17/GRCh38#79934835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119033205-C-A

79934835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033205-C-G

79934835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033205-C-T

http://identifiers.org/hco/17/GRCh38#79934839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119033209-C-A

79934839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033209-C-T

79934845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033215-G-A

79934845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033215-G-T

http://identifiers.org/hco/17/GRCh38#79934986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119033307-C-A

79934986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033307-C-T

http://identifiers.org/hco/17/GRCh38#79935111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119033457-C-A

http://identifiers.org/hco/17/GRCh38#79935122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119033468-C-A

79935122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033468-C-T

79935173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033518-G-A

79935173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033518-G-T

79935183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033528-G-A

79935212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033553-G-A

79935212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033553-G-T

79935256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033595-C-T

79935259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033598-G-A

79935259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033598-G-T

http://identifiers.org/hco/17/GRCh38#79935280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119033617-C-A

79935280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033617-C-T

79935282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033619-T-A

79935282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033619-T-C

79935306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033625-G-A

79935306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033625-G-T

79935443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033711-G-A

79935443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033711-G-T

79935531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033781-T-C

79935531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033781-T-G

http://identifiers.org/hco/17/GRCh38#79935583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119033825-C-A

79935583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033825-C-G

79935583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033825-C-T

79935684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033919-T-C

http://identifiers.org/hco/17/GRCh38#79935720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119033946-C-A

79935731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119033957-C-T

http://identifiers.org/hco/17/GRCh38#79935784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119033998-C-A

http://identifiers.org/hco/17/GRCh38#79936004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119034205-C-A

79936092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119034252-G-A

79936092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119034252-G-T

79936133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119034268-A-G

79936255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119034398-C-T

79936314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119034459-G-T

http://identifiers.org/hco/17/GRCh38#79936322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119034467-C-A

79936341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119034486-C-T

79936397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119034542-A-G

http://identifiers.org/hco/17/GRCh38#79936638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119034667-C-A

79936638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119034667-C-T

79936662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119034690-G-T

79936685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119034713-G-A

79936697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119034725-T-C

79936742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119034755-G-A

79936742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119034755-G-T

79936766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119034783-C-T

79936773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119034787-G-A

79936773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119034787-G-C

79936773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119034787-G-T

79936971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119034969-C-T

http://identifiers.org/hco/17/GRCh38#79937031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119035014-C-A

79937031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119035014-C-T

79937055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 119035036-A-G

http://identifiers.org/hco/17/GRCh38#79937065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119035046-C-A

79937065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119035046-C-T

79937070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119035051-A-G

79937317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119035284-T-C

79937347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119035314-G-T

79937417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119035367-G-T

79937427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119035376-G-A

79937427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119035376-G-T

http://identifiers.org/hco/17/GRCh38#79937443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119035392-C-A

79937465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119035404-T-C

79937509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119035456-C-G

79937509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119035456-C-T

79937522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119035469-A-G

http://identifiers.org/hco/17/GRCh38#79937546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119035491-C-A

http://identifiers.org/hco/17/GRCh38#79937556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119035501-C-A

79937557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119035502-A-G

http://identifiers.org/hco/17/GRCh38#79937568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119035504-C-A

79937568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119035504-C-T

79937580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119035516-G-T

http://identifiers.org/hco/17/GRCh38#79937706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119035625-C-A

http://identifiers.org/hco/17/GRCh38#79937826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119035760-C-A

79937826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119035760-C-T

http://identifiers.org/hco/17/GRCh38#79937877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119035826-C-A

79937877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119035826-C-T

http://identifiers.org/hco/17/GRCh38#79937899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119035850-C-A

79937975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119035907-T-A

79938002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119035934-G-T

79938044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119035975-G-A

79938195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119036125-G-A

79938195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119036125-G-T

79938206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119036136-A-T

79938232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119036161-G-A

79938232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119036161-G-T

http://identifiers.org/hco/17/GRCh38#79938259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119036184-C-A

79938259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119036184-C-G

79938317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119036232-A-G

http://identifiers.org/hco/17/GRCh38#79938458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119036345-C-A

http://identifiers.org/hco/17/GRCh38#79938485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119036372-C-A

79938485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119036372-C-T

http://identifiers.org/hco/17/GRCh38#79938617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119036454-C-A

79938617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119036454-C-T

79938695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119036506-A-G

79938920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119036692-T-C

http://identifiers.org/hco/17/GRCh38#79938940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119036715-C-A

79938940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119036715-C-T

79939059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119036835-A-G

79939313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119037029-A-G

79939339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119037056-A-G

http://identifiers.org/hco/17/GRCh38#79939391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119037102-C-A

79939391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119037102-C-T

79939836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119037577-C-T

79939919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119037662-T-C

79939958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119037694-C-T

http://identifiers.org/hco/17/GRCh38#79940079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119037760-C-A

79940138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119037800-G-C

79940159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119037813-G-T

79940224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119037908-A-T

79940225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119037909-A-G

79940301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119037971-G-T

79940341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119038009-G-T

79940342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119038010-G-T

79940368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119038034-G-A

79940468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119038078-G-T

79940470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119038080-G-T

79940535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119038115-G-A

79940535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119038115-G-T

http://identifiers.org/hco/17/GRCh38#79940654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119038217-C-A

79940654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119038217-C-T

79940674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119038234-G-T

http://identifiers.org/hco/17/GRCh38#79940679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119038235-C-A

79940679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3 prime UTR variant
orthologous variants: 119038235-C-T

79940713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119038266-T-C

79940727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119038280-T-C

79940777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119038313-T-A

79940777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119038313-T-C

http://identifiers.org/hco/17/GRCh38#79940797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119038335-C-A

79940797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119038335-C-T

79940810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119038348-G-A

79940810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119038348-G-T

http://identifiers.org/hco/17/GRCh38#79940812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119038350-C-A

79940812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119038350-C-T

79940831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119038368-A-G

http://identifiers.org/hco/17/GRCh38#79940834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119038371-C-A

79940834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119038371-C-T

http://identifiers.org/hco/17/GRCh38#79940858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3_prime_UTR_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119038393-C-A

79940858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 3_prime_UTR_variant, splice_donor_variant
orthologous variants: 119038393-C-T

http://identifiers.org/hco/17/GRCh38#79940886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119038421-C-A

79940886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119038421-C-T

79940985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119038520-G-A

79940985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119038520-G-C

79941099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119038634-A-G

79941488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119038936-C-T

79941516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119038965-T-G

79941540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119038994-C-T

79941635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119039073-G-A

79941677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119039126-C-T

79941808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119039236-C-G

79941847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119039294-C-T

79941876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119039331-A-T

79941878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119039333-G-T

http://identifiers.org/hco/17/GRCh38#79941958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#119039441-C-A

79941958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119039441-C-T

http://identifiers.org/hco/17/GRCh38#79941970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#119039453-C-A

79941970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119039453-C-T

79941977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119039481-A-G

http://identifiers.org/hco/17/GRCh38#79941979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119039483-C-A

79942033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119039726-T-A

79942033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119039726-T-C

79942033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119039726-T-G

79942034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119039727-G-A

79942034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119039727-G-T

http://identifiers.org/hco/17/GRCh38#79942039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#119039732-C-A

79942039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119039732-C-T

79942040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119039733-C-G

http://identifiers.org/hco/17/GRCh38#79942045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#119039739-C-A

79942045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119039739-C-G

79942066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous_variant, undefined
orthologous variants: 119039763-G-T

79942081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous_variant, undefined
orthologous variants: 119039778-G-A

79942098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: missense variant
orthologous variants: 119039795-G-C

79942105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119039802-G-A

79942126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous_variant, undefined
orthologous variants: 119039823-C-G

79942126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous_variant, undefined
orthologous variants: 119039823-C-T

79942167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: missense variant
orthologous variants: 119039864-C-T

79942171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119039868-G-A

79942218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119039918-G-A

79942218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119039918-G-T

79942221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119039921-A-G

79944292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119041257-T-C

79944466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119041416-C-G

79944780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119041686-G-A

79944780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119041686-G-C

79944780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119041686-G-T

79944819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119041724-G-A

79944819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119041724-G-C

79944819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119041724-G-T

79944839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119041754-G-A

79944839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119041754-G-T

79944917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119041863-G-A

79944917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119041863-G-T

79944947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119041893-T-C

79944947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: missense variant
orthologous variants: 119041893-T-G

79945087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 119042033-G-A

79945087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 119042033-G-T

http://identifiers.org/hco/17/GRCh38#79945106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119042052-C-A

79945106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119042052-C-T

http://identifiers.org/hco/17/GRCh38#79945138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119042084-C-A

79945138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119042084-C-T

http://identifiers.org/hco/17/GRCh38#79945435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119043096-C-A

79945547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119043173-G-A

79945920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119043507-A-T

http://identifiers.org/hco/17/GRCh38#79947599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119044673-C-A

79947599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119044673-C-T

79947600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119044674-G-A

79947600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119044674-G-C

79947628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119044702-A-G

79947849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119044917-C-T

79948444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119045543-C-T

79948589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119045692-G-T

79948655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119045749-G-C

79948664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119045757-C-T

79948680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119045773-G-C

http://identifiers.org/hco/17/GRCh38#79948737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119045820-C-A

http://identifiers.org/hco/17/GRCh38#79948803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119045841-C-A

79948803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119045841-C-T

79948822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119045860-G-A

79949106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119046194-T-G

79949445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119046607-G-A

79949497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119046660-A-T

79949499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119046662-G-A

79949697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119046830-G-A

79949703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119046833-G-A

79949708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119046838-G-A

79949708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119046838-G-T

79949770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119046899-C-G

79949873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 119047002-A-G

http://identifiers.org/hco/17/GRCh38#79950104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119047246-C-A

79950105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119047247-G-A

http://identifiers.org/hco/17/GRCh38#79950268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119047361-C-A

79950268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119047361-C-T

http://identifiers.org/hco/17/GRCh38#79950272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119047365-C-A

79950272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119047365-C-T

http://identifiers.org/hco/17/GRCh38#79950417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119047475-C-A

79950417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119047475-C-T

79950498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: missense variant
orthologous variants: 119047556-C-G

79950522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119047580-C-G

79950522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119047580-C-T

79950726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119047787-T-C

79950726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119047787-T-G

79950812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119047860-G-A

79950812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119047860-G-C

79951044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119048097-G-A

79951051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119048106-G-A

79951102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119048162-G-T

http://identifiers.org/hco/17/GRCh38#79951318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119048382-A-C

79951318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119048382-A-T

http://identifiers.org/hco/17/GRCh38#79951360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119048421-C-A

http://identifiers.org/hco/17/GRCh38#79951438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119048554-C-A

http://identifiers.org/hco/17/GRCh38#79951563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119048679-C-A

79951563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 119048679-C-T

79951565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 119048681-A-G

79951582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 119048698-G-A

79951710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119048815-G-T

79951876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119048943-G-A

79951876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119048943-G-C

79951876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119048943-G-T

79952001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, missense_variant
orthologous variants: 119049028-T-C

http://identifiers.org/hco/17/GRCh38#79952059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119049085-C-A

79952059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, missense_variant
orthologous variants: 119049085-C-G

79952059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, missense_variant
orthologous variants: 119049085-C-T

79952180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 119049161-G-A

79952180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 119049161-G-T

79952287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119049228-G-A

79952287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119049228-G-T

79952484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119049364-C-T

79952535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119049414-G-A

79952535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119049414-G-C

79952535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119049414-G-T

79952550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119049429-A-G

http://identifiers.org/hco/17/GRCh38#79952637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119049539-C-A

79952637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119049539-C-T

http://identifiers.org/hco/17/GRCh38#79952900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#119049793-C-A

79952900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119049793-C-T

79952966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119049863-T-C

79952968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119049865-T-C

79952994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119049898-T-A

79953027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119049976-A-G

79953267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119050185-G-A

79970174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119059260-C-T

79970419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119059508-A-G

http://identifiers.org/hco/17/GRCh38#79970535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119059615-A-C

79970557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119059637-C-T

79970728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119059794-G-A

http://identifiers.org/hco/17/GRCh38#79970928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119059928-C-A

79970930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119059930-T-A

http://identifiers.org/hco/17/GRCh38#79970966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#119059964-A-C

79975303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119064381-G-A

79975521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119064564-G-A

79975545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119064588-A-G

79975574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119064617-C-T

79975643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119064698-C-G

79975792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119064841-G-A

79975792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119064841-G-T

79975820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119064866-C-T

http://identifiers.org/hco/17/GRCh38#79975856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119064902-C-A

79976003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119065016-G-A

http://identifiers.org/hco/17/GRCh38#79977211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119066807-C-A

79977545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119067099-G-A

79977594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119067131-G-A

79977686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119067207-A-G

http://identifiers.org/hco/17/GRCh38#79977741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119067289-C-A

79977741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119067289-C-T

79978040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119067587-T-A

79978503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119068020-G-A

79978630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119068150-G-A

79978690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119068183-G-A

79978883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119068358-T-G

79978953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119068413-C-T

79978996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119068523-A-G

79979074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119068686-A-G

79979134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119068735-C-T

79979256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119068864-G-T

79979408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119068974-T-A

79979618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119069116-T-C

79979706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119069160-G-A

79979882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119069326-C-T

79979888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119069333-G-A

79980080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119069436-C-T

79980322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119069681-G-A

79980394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119069732-G-A

79980483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119069797-G-C

79981071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119070964-T-C

79981250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119071141-T-A

79983074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119072353-G-A

79983112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119072391-C-G

79983163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119072434-A-G

http://identifiers.org/hco/17/GRCh38#79984885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119073563-C-A

79984885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119073563-C-G

79984885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119073563-C-T

http://identifiers.org/hco/17/GRCh38#79985008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119073677-C-A

79985437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119074000-C-T

79985568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119074115-G-A

79986146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119074663-G-T

79986175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119074692-G-A

79986190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119074707-G-A

79986508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119075004-A-G

79986655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119075144-T-C

79986950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119075363-C-T

79987182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119075469-T-C

79987448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119075695-T-A

http://identifiers.org/hco/17/GRCh38#79987857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119076046-C-A

79987857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119076046-C-T

79987886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119076072-G-T

79988196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119077338-T-A

79988250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119077391-G-A

79988406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119077541-T-C

79990128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119079279-G-C

79990225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119079338-C-T

79990244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119079353-A-G

79990252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119079361-T-C

79990341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119079423-G-A

http://identifiers.org/hco/17/GRCh38#79991240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119081027-C-A

79991414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119081160-C-T

79991747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081419-G-A

79991945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081610-G-A

79991945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081610-G-T

79991946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081611-G-A

79991946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081611-G-T

http://identifiers.org/hco/17/GRCh38#79992001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#119081663-C-A

79992001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081663-C-G

79992027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081682-C-G

79992027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081682-C-T

79992028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081683-G-A

79992028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081683-G-T

79992196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081785-T-C

79992281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081862-T-A

79992281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081862-T-C

79992285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081866-G-T

79992301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081881-G-T

79992319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081899-G-A

79992319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081899-G-T

79992354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081941-A-T

79992382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081969-G-A

79992382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081969-G-T

79992396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119081983-C-T

79992470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119082031-G-A

79992472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119082034-A-T

79992550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119082108-G-A

79992561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119082119-C-T

79993394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 119082423-C-T

79993456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 119082498-G-T

http://identifiers.org/hco/17/GRCh38#79993516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119082539-C-A

79993516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119082539-C-T

79993539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119082563-A-G

79993543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119082567-C-T

79993672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 119082674-T-C

79993692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 119082694-G-A

79993692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 119082694-G-T

79993709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 119082704-A-G

79993862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 119082781-G-A

80000134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119088515-C-T

80000193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119088570-G-C

80000241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119088613-A-G

80000434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119088763-C-T

80000617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119088857-G-A

80001074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119089376-C-T

80001938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119090114-G-C

80001938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119090114-G-T

80002046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119090223-G-A

80005919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119094382-T-G

80005947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119094411-C-T

80005949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119094413-C-T

80005991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119094452-G-A

80007236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119096475-G-C

http://identifiers.org/hco/17/GRCh38#80007251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119096491-C-A

80007261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119096501-G-A

80007302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119096543-C-T

http://identifiers.org/hco/17/GRCh38#80007462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119096676-C-A

80007466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119096680-C-T

80007585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119096795-G-A

80007654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119096853-C-T

80007697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119096885-G-A

http://identifiers.org/hco/17/GRCh38#80008231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119097380-C-A

80008279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119097427-G-A

80008395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119097515-G-A

80008445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119097522-C-T

80008542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119097561-G-A

80008589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119097607-T-G

80008592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119097611-G-A

80008724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119097689-C-T

80008725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119097690-G-A

80008804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119097765-G-A

80008875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119097835-C-T

80008995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119097916-T-C

80009118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119098006-T-C

80009203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119098086-A-G

80009213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119098096-C-G

80009302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119098182-A-G

80009303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119098183-T-C

80009595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119099057-C-T

80009596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119099058-G-A

80009743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119099263-G-A

80009743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119099263-G-C

80009752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119099272-A-G

80009846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119099368-G-A

80010099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119099551-T-C

80010114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119099569-G-T

80010144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119099581-A-G

80010145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119099582-G-C

80010151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119099588-G-A

80010207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119099644-C-T

80010246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119099683-G-A

80010246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: missense variant
orthologous variants: 119099683-G-T

80010255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119099692-T-C

80010424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: missense variant
orthologous variants: 119099861-C-T

80010612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119100049-G-C

80010666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119100103-G-A

80010666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: missense variant
orthologous variants: 119100103-G-C

80010666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: missense variant
orthologous variants: 119100103-G-T

http://identifiers.org/hco/17/GRCh38#80010672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119100109-C-A

80010672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119100109-C-T

80010693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119100130-G-T

80010770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119100207-A-G

http://identifiers.org/hco/17/GRCh38#80010780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119100217-C-A

80010780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119100217-C-T

80011987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119100445-G-A

80012036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119100454-G-A

80012036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119100454-G-T

80013361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119101325-G-A

80013361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119101325-G-T

80013407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: synonymous variant
orthologous variants: 119101371-G-A

80013559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 5 prime UTR variant
orthologous variants: 119101520-T-C

80013632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119101590-A-G

http://identifiers.org/hco/17/GRCh38#80013653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119101617-C-A

80013653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119101617-C-G

80013653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119101617-C-T

80019052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119102556-T-C

80019125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119102631-C-T

80019275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119102731-G-C

80019410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119102850-C-T

http://identifiers.org/hco/17/GRCh38#80019460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119102891-A-C

80019460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119102891-A-G

80019460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119102891-A-T

http://identifiers.org/hco/17/GRCh38#80026406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119109490-C-A

80026564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119109576-G-A

80026668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119109647-G-A

80026706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119109684-G-C

80026938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119109849-A-T

80026951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119109862-C-G

80026951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119109862-C-T

80028973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119110996-G-C

80029208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119111159-C-T

80029761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119112644-G-A

80029761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119112644-G-C

80029761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119112644-G-T

80029854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119112732-T-C

80029863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119112746-C-T

80029979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119112808-C-T

80029987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119112816-G-A

80030056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119112881-C-T

80030178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119113058-G-A

80030178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119113058-G-C

80030233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119113094-G-C

80030296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119113156-C-G

80030296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119113156-C-T

80030425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119113266-C-T

80030487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119113333-G-T

80030558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119113511-A-T

80030565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119113626-C-T

80030798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119113833-G-T

80030815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119113850-G-A

80030815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119113850-G-C

80030892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119113920-G-A

80030892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119113920-G-C

80030970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119113996-C-G

80030970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119113996-C-T

80030996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron_variant, undefined
orthologous variants: 119114021-C-T

80031296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119114205-A-T

80031406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119114286-A-T

80031468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119114351-G-A

80031526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119114398-C-T

80031718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119114586-G-C

80031774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119114655-G-A

80031776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119114657-G-A

80031776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119114657-G-C

80032868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119116190-G-A

80032868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119116190-G-C

80035065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119118542-G-C

80035526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119118987-G-A

80035574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119119033-C-T

80035582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119119041-A-T

80035659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119119099-G-A

80035659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119119099-G-T

80035767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119119194-G-A

http://identifiers.org/hco/17/GRCh38#80035778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119119205-C-A

80035778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: intron variant
orthologous variants: 119119205-C-T

80035840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 5 prime UTR variant
orthologous variants: 119119267-G-A

80035843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 5 prime UTR variant
orthologous variants: 119119270-A-G

80035843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28356
most severe consequence: 5 prime UTR variant
orthologous variants: 119119270-A-T