46575797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5 prime UTR variant
orthologous variants: 85941929-T-C

http://identifiers.org/hco/22/GRCh38#46575883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85941987-A-C

46575938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85942051-A-G

46575997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85942141-G-A

46575997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85942141-G-T

46575998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85942142-A-G

46575999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85942143-G-T

46576395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85942439-G-A

http://identifiers.org/hco/22/GRCh38#46576504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85942540-A-C

46576569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85942555-C-G

46576733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, undefined
orthologous variants: 85942722-T-C

46576815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85942765-C-T

46576886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, undefined
orthologous variants: 85942823-G-A

46576946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85942884-A-G

46577020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85942916-G-C

http://identifiers.org/hco/22/GRCh38#46577076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85942951-C-A

46577076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85942951-C-G

46577076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85942951-C-T

46577077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85942952-C-T

46577268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 85943140-G-A

46577268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 85943140-G-T

http://identifiers.org/hco/22/GRCh38#46577346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85943215-C-A

46577346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85943215-C-T

http://identifiers.org/hco/22/GRCh38#46577375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85943243-A-C

46577375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85943243-A-G

http://identifiers.org/hco/22/GRCh38#46577389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85943253-C-A

46577389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85943253-C-T

46578062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85943895-G-A

46578178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85943981-G-A

46578178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85943981-G-T

46578202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85944006-T-C

46578207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85944011-T-C

46578248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85944067-G-A

46578424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85944231-G-A

46578424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85944231-G-C

46578456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85944263-G-A

46578497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85944303-G-C

46578497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85944303-G-T

46578654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, undefined
orthologous variants: 85944461-G-A

46579196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, undefined
orthologous variants: 85944892-C-G

46579289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85945000-G-A

46579294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85945005-C-T

46579413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85945130-T-A

46579413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85945130-T-C

46579413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85945130-T-G

46579635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85945303-G-A

46579710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85945372-C-T

46579737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85945397-G-A

46580226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85945840-G-A

46580343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85945960-G-A

46581448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85946654-G-A

46581498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85946677-C-G

46581623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85946743-G-T

46581680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85946807-A-T

46581686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85946813-G-A

http://identifiers.org/hco/22/GRCh38#46581709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85946836-C-A

46581709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85946836-C-T

46584832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85949023-T-A

46584859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85949051-C-G

46584914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85949111-A-T

46585061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85949257-T-C

46585094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85949286-A-G

46586742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85950178-G-T

46586803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85950246-G-C

46586928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85950366-G-A

46587439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85951333-C-T

http://identifiers.org/hco/22/GRCh38#46587455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85951361-C-A

46587455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85951361-C-G

http://identifiers.org/hco/22/GRCh38#46587606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85951526-C-A

http://identifiers.org/hco/22/GRCh38#46587797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85951851-C-A

46587797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85951851-C-T

http://identifiers.org/hco/22/GRCh38#46587844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85951924-C-A

46587844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85951924-C-T

46587886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85951961-G-A

46587985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85952102-T-C

46588340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85952397-G-A

46588562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85952590-G-A

46588571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85952599-A-T

46588588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85952613-G-A

46588788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85952817-C-G

46588788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85952817-C-T

46588920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85952956-C-T

46589053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85953080-G-A

46589053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85953080-G-C

46589086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85953105-G-A

http://identifiers.org/hco/22/GRCh38#46589253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85953231-A-C

46589290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85953243-C-T

46589528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85953395-G-A

46589542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85953409-T-C

46589827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85953695-T-C

46589834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85953702-C-T

46589894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85953770-T-C

46592054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85954355-G-A

46592174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85954479-G-C

46592685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, undefined
orthologous variants: 85954882-T-A

46592685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, undefined
orthologous variants: 85954882-T-C

46592916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85955071-A-G

46592916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85955071-A-T

http://identifiers.org/hco/22/GRCh38#46592920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85955075-A-C

46592920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, undefined
orthologous variants: 85955075-A-G

46592922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, undefined
orthologous variants: 85955077-A-G

46593078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85955239-T-C

46593188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85955339-A-T

46593326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85955465-C-T

46593376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, undefined
orthologous variants: 85955498-G-A

46593444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, undefined
orthologous variants: 85955566-A-G

46593491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, undefined
orthologous variants: 85955601-A-G

46595376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: -T-C

http://identifiers.org/hco/22/GRCh38#46595383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: -C-A

46595420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: -C-T

46595429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: -C-T

46595496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: -C-G

http://identifiers.org/hco/22/GRCh38#46595613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: -C-A

46595613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: -C-T

46595625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: -C-T

46595699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: -A-G

46595851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: -C-T

46595999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: -C-G

46596323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, undefined
orthologous variants: -G-C

46597109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: -T-C

46599772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: -C-T

46599875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: -G-A

46599875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: -G-C

46599875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: -G-T

46599947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: -G-A

46610126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85966537-C-T

46610350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85966726-G-A

46610586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85966902-T-C

46610719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85967013-G-A

46611329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85967286-G-A

46611388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85967293-G-A

46611503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85967388-C-T

46619223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85969219-T-C

46619913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85970312-G-A

46620002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85970409-C-T

46620031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85970442-G-A

46620047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85970458-A-G

46620062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85970473-G-A

http://identifiers.org/hco/22/GRCh38#46620083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85970499-C-A

46620083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85970499-C-T

46620121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85970539-T-A

http://identifiers.org/hco/22/GRCh38#46620180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85970597-A-C

46620238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85970657-G-T

http://identifiers.org/hco/22/GRCh38#46620246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85970665-C-A

http://identifiers.org/hco/22/GRCh38#46620256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85970675-C-A

46620256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85970675-C-T

46620342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85970731-G-A

46620342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85970731-G-T

46620370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85970762-G-A

46620370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85970762-G-T

46620386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85970778-G-A

46620386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85970778-G-T

http://identifiers.org/hco/22/GRCh38#46620387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85970779-C-A

46620387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85970779-C-T

46620421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85970811-A-G

http://identifiers.org/hco/22/GRCh38#46620581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85970968-C-A

46620581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85970968-C-G

46620581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85970968-C-T

46620602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85970985-A-G

46620642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971025-G-A

46620642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971025-G-T

46620670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971056-A-G

46620688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971074-G-A

46620688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971074-G-T

46620700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971086-T-A

46620712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971102-C-T

46620727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971119-G-A

46620794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971171-G-T

46620799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971176-G-T

46621105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971439-T-G

46621128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971460-T-C

46621137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971519-C-T

46621158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971537-G-A

46621158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971537-G-T

46621287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971673-G-A

46621439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971786-C-T

46621839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971842-C-T

46621897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971899-G-A

46621939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971932-C-T

46621975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85971978-C-T

46621991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85972001-C-G

46621991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85972001-C-T

46622331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85972317-C-G

46622338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85972324-C-T

46622376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85972386-C-T

46624737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85973712-C-G

46624737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85973712-C-T

46625106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85974022-C-T

http://identifiers.org/hco/22/GRCh38#46625221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85974111-C-A

46625459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85974337-C-T

46625717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85974669-G-C

46625822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85974777-G-A

46625828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85974783-G-A

46625902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85974859-C-G

46625902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85974859-C-T

46625917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85974874-C-G

46625917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85974874-C-T

46626202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85975072-C-G

46626202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85975072-C-T

http://identifiers.org/hco/22/GRCh38#46626270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85975125-C-A

46626270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85975125-C-T

46626392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85975264-G-C

46626627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85975449-A-G

46626700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85975459-G-A

46626700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85975459-G-C

46626715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85975474-G-A

http://identifiers.org/hco/22/GRCh38#46626735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85975492-C-A

46626735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85975492-C-T

46626865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85975628-G-A

http://identifiers.org/hco/22/GRCh38#46626981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85975757-C-A

46626988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85975764-G-A

46626996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85975787-G-C

46627003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85975794-G-A

46627023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85975816-G-A

46627029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85975822-G-T

46627207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85975985-T-A

46627229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85976007-C-T

46627564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85976314-T-C

46627637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85976426-C-T

46627731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85976529-G-A

46627819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85976616-G-A

46627901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85976697-C-T

46627902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85976698-G-A

46627902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85976698-G-C

46627968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85976785-G-A

46628115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85976910-G-T

46628692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85978879-A-G

46628729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85978916-G-A

46628793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85978975-G-A

46628816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85978999-G-T

46628884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85979049-C-T

46629094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85979246-G-A

46629094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85979246-G-C

46629177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85979346-C-T

46629246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85979406-T-A

46629250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85979410-C-T

46629648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85979788-G-A

46633398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85982747-T-C

46633492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85982848-C-G

46633623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85982986-C-T

46633740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85983080-G-C

46633740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85983080-G-T

46633755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85983095-C-G

46634050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85983337-T-C

46634292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85983559-G-A

46634344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85983610-A-G

46637899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85985040-T-C

46637911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 85985052-T-G

46637935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 85985076-T-G

46638014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85985193-T-C

46638022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85985201-G-C

46638022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85985201-G-T

46638048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85985223-G-A

46638048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85985223-G-C

http://identifiers.org/hco/22/GRCh38#46638091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85985268-C-A

46638091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85985268-C-T

http://identifiers.org/hco/22/GRCh38#46638105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85985289-C-A

46638105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85985289-C-T

46638450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85985599-A-G

46638465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85985620-G-C

46638482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85985637-G-A

http://identifiers.org/hco/22/GRCh38#46638588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85985744-C-A

http://identifiers.org/hco/22/GRCh38#46638592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85985748-A-C

46638703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85985854-C-T

46640554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85986201-G-A

46640756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85986541-A-G

46640842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85986589-G-A

46645091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85989711-G-C

46645092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85989712-G-A

46645416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85990136-G-A

http://identifiers.org/hco/22/GRCh38#46645615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85990331-A-C

46645615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85990331-A-G

46645847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85990564-T-A

46645912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85990632-T-C

46645931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85990651-G-A

46645933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85990653-G-A

46645933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85990653-G-C

46645944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85990664-C-T

46646312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85990969-A-G

http://identifiers.org/hco/22/GRCh38#46646424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85991077-C-A

46646646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85991282-T-A

46646646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85991282-T-C

46646647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85991283-C-T

46647755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85992169-C-T

http://identifiers.org/hco/22/GRCh38#46647810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85992252-C-A

46647874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85992320-G-A

46647925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85992352-C-T

46649075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85992630-T-C

46649125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85992679-C-T

46649659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85993566-T-A

46649747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85993657-A-G

46649867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85993752-G-A

46650471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85994154-C-T

46650513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85994188-C-T

46650529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85994203-C-G

46650529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85994203-C-T

46650654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85994314-A-T

46650735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85994390-G-T

46650898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85994544-G-A

46651083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85994717-G-A

46651170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85994829-C-T

46651213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85994871-G-T

46651254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85994911-C-G

46651310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85994968-C-G

46651620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85995226-C-G

46651748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85995359-G-T

46651846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85995452-G-A

46651924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85995548-G-A

46652098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85995710-C-T

46652199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85995797-G-A

46652283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, undefined
orthologous variants: 85995888-A-G

46652317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, undefined
orthologous variants: 85995922-G-A

46654057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85999016-G-T

46654213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85999670-C-G

46654439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 85999892-C-T

46656695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86000357-C-T

http://identifiers.org/hco/22/GRCh38#46656903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86000537-A-C

46657031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86000622-A-G

46657054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86000645-T-C

46657096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86000699-C-T

46657099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86000702-C-T

46657613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86002122-C-T

46657703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86002215-C-G

46657819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86002320-T-G

http://identifiers.org/hco/22/GRCh38#46658041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86002531-C-A

46658041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86002531-C-T

http://identifiers.org/hco/22/GRCh38#46658051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86002541-A-C

46658051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86002541-A-G

46658148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86002627-A-T

46658313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86002790-G-A

46658529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86003412-C-T

46658531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86003414-C-G

46658603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86003479-G-C

46658612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86003488-T-A

46658612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86003488-T-C

http://identifiers.org/hco/22/GRCh38#46660071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86004880-C-A

46660172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86004987-G-A

46660183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86004998-C-T

46660327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86005095-C-T

46660352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86005120-G-A

46660352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86005120-G-T

46660447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86005191-G-A

46661002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86006032-C-T

46661146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86006182-T-C

46661178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86006214-C-T

46661179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86006215-G-A

46661205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86006241-T-C

http://identifiers.org/hco/22/GRCh38#46661270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86006302-C-A

46661270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86006302-C-T

http://identifiers.org/hco/22/GRCh38#46661292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86006322-C-A

46661292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86006322-C-T

46661301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86006331-G-A

46661301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86006331-G-T

46661361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86006373-T-C

46661574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, undefined
orthologous variants: 86006474-C-T

http://identifiers.org/hco/22/GRCh38#46661585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86006485-C-A

46661585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86006485-C-T

46662061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86008323-G-A

46662071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86008333-A-T

46662252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86008505-C-T

46662290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86008528-G-A

46662304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86008540-A-G

http://identifiers.org/hco/22/GRCh38#46662520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86008844-C-A

46662520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86008844-C-G

http://identifiers.org/hco/22/GRCh38#46662701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86008965-A-C

http://identifiers.org/hco/22/GRCh38#46662720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86008982-C-A

46662720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86008982-C-T

46663006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86009288-T-G

46663012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86009294-G-A

46663012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86009294-G-C

46663029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86009311-G-T

46663164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: synonymous variant
orthologous variants: 86009449-C-T

http://identifiers.org/hco/22/GRCh38#46663185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86009473-C-A

46663185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86009473-C-G

46663185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86009473-C-T

46663223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86009508-T-C

46663235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86009519-G-A

46663235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86009519-G-T

46663242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86009526-G-A

46663390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86009648-T-C

46663443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86009713-A-G

46663491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86009761-T-G

46663525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86009797-T-C

46663733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86009915-G-T

46663736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86009918-G-A

46663736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86009918-G-T

http://identifiers.org/hco/22/GRCh38#46663989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86011152-C-A

46663989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011152-C-G

46663989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011152-C-T

http://identifiers.org/hco/22/GRCh38#46664014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86011178-C-A

46664014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011178-C-G

46664014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011178-C-T

46664030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: synonymous variant
orthologous variants: 86011194-C-T

46664054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: synonymous variant
orthologous variants: 86011218-T-C

46664152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011317-T-C

46664152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011317-T-G

46664174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011339-A-G

46665406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011532-C-T

http://identifiers.org/hco/22/GRCh38#46665434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86011565-C-A

46665435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011566-C-T

46665490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011617-G-A

46665490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011617-G-T

46665514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011635-G-A

46665514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011635-G-T

46665554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011666-G-A

46665554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011666-G-T

46665558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011670-G-A

46665558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011670-G-T

46665563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011675-T-C

46665577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011687-G-T

46665638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: synonymous variant
orthologous variants: 86011774-T-C

http://identifiers.org/hco/22/GRCh38#46665853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86011982-C-A

46665853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011982-C-G

46665853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86011982-C-T

46665911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86012023-A-G

46666040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86012107-C-T

46666089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86012146-G-T

46666094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86012151-A-G

46666443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86012454-C-T

46666891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86012934-G-A

46667035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86013034-T-C

46667753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86013519-C-G

46667835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86013635-C-T

http://identifiers.org/hco/22/GRCh38#46667970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86013719-C-A

46667970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86013719-C-T

46667986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86013734-T-C

46667986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86013734-T-G

46668010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86013766-G-A

46668010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86013766-G-C

46668531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86014200-C-T

46668554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86014217-T-C

http://identifiers.org/hco/22/GRCh38#46668573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86014236-C-A

46668573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86014236-C-T

46668577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86014240-A-G

46668577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86014240-A-T

46668578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86014241-G-A

46668578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86014241-G-T

46668769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86014429-G-A

46668769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86014429-G-C

46668769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86014429-G-T

46668908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 86014567-G-A

46668908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: missense_variant, splice_region_variant, stop_gained
orthologous variants: 86014567-G-T

46672754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86014638-G-T

46672761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86014645-G-T

http://identifiers.org/hco/22/GRCh38#46672781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86014665-C-A

46672781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86014665-C-G

46672781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86014665-C-T

46672826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86014682-G-A

46672826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86014682-G-C

46673010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86014869-C-T

46673672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 86016057-G-T

46673765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: synonymous variant
orthologous variants: 86016150-C-T

46673807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: synonymous variant
orthologous variants: 86016192-G-A

46673823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86016208-G-A

46673824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86016209-C-G

46673825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86016210-C-G

46673825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86016210-C-T

http://identifiers.org/hco/22/GRCh38#46673937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86016317-C-A

46673937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86016317-C-T

http://identifiers.org/hco/22/GRCh38#46673954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86016326-C-A

46673954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86016326-C-T

http://identifiers.org/hco/22/GRCh38#46673955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86016327-C-A

46673955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86016327-C-G

46673958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86016330-G-T

http://identifiers.org/hco/22/GRCh38#46673982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86016357-A-C

46673982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86016357-A-G

46674294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86016646-C-T

http://identifiers.org/hco/22/GRCh38#46674314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86016667-A-C

46674355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86016747-G-A

46674637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 86016997-G-A

http://identifiers.org/hco/22/GRCh38#46674715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86017074-C-A

46674777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86017136-G-A

46674777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86017136-G-C

http://identifiers.org/hco/22/GRCh38#46674806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86017168-C-A

46674806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86017168-C-T

46674830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86017191-G-A

46674830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86017191-G-T

46674846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86017209-T-G

46675049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86017393-G-C

46675049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86017393-G-T

46675139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86017550-T-C

46675383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86017791-A-G

46675434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86017840-A-T

46675564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86017970-T-A

46675564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86017970-T-C

46675564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86017970-T-G

46675659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86018164-G-A

46675659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86018164-G-T

http://identifiers.org/hco/22/GRCh38#46675672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86018177-C-A

46675672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86018177-C-T

46675774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86018339-G-A

46675781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86018346-T-C

46675784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86018349-G-A

46675784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86018349-G-T

46675834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86018440-C-T

http://identifiers.org/hco/22/GRCh38#46676477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86018926-C-A

46676490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86018950-G-T

46676523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86018995-T-C

46676524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86018996-G-T

http://identifiers.org/hco/22/GRCh38#46676532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86019004-C-A

46676532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86019004-C-T

46676623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 86019105-A-G

46676690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86019172-G-A

46676690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86019172-G-T

http://identifiers.org/hco/22/GRCh38#46676742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86019214-A-C

46676742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86019214-A-G

46676767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86019235-T-C

46676767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86019235-T-G

http://identifiers.org/hco/22/GRCh38#46676789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86019253-A-C

http://identifiers.org/hco/22/GRCh38#46676799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86019263-C-A

46676799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86019263-C-T

46676800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86019264-T-A

46676800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86019264-T-C

http://identifiers.org/hco/22/GRCh38#46676805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86019269-C-A

46676805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86019269-C-T

46677062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86019471-G-A

46677117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86019514-T-A

46677117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86019514-T-C

http://identifiers.org/hco/22/GRCh38#46677119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86019516-C-A

http://identifiers.org/hco/22/GRCh38#46677239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86019643-C-A

46677239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 86019643-C-T

46677308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86019682-T-C

46677349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86019718-A-G

46677349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86019718-A-T

46677457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86019826-C-T

http://identifiers.org/hco/22/GRCh38#46677458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86019827-C-A

46677509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86019870-G-A

46677509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86019870-G-T

46677527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86019888-C-T

http://identifiers.org/hco/22/GRCh38#46677561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86019946-C-A

46677561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86019946-C-T

46677713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020091-T-G

46677782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020152-C-G

46677782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020152-C-T

46677970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020267-T-C

46677970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020267-T-G

46677983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020281-G-A

46677983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020281-G-C

46677983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020281-G-T

46678004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020302-C-T

46678027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020330-G-A

46678027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020330-G-T

46678028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020331-A-G

46678050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020353-G-A

46678050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020353-G-T

http://identifiers.org/hco/22/GRCh38#46678095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86020405-C-A

46678095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020405-C-T

46678320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020554-T-C

http://identifiers.org/hco/22/GRCh38#46678397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86020633-C-A

46678397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020633-C-T

http://identifiers.org/hco/22/GRCh38#46678417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86020654-A-C

46678417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020654-A-G

46678462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020681-A-G

http://identifiers.org/hco/22/GRCh38#46678551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86020719-C-A

46678551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020719-C-G

46678551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020719-C-T

46678738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86020904-A-G

46678869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86021023-T-A

46678869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86021023-T-C

http://identifiers.org/hco/22/GRCh38#46678898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86021051-C-A

46678898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86021051-C-G

46678898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86021051-C-T

46678902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86021055-G-T

46678913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86021065-C-T

46678932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86021084-A-G

http://identifiers.org/hco/22/GRCh38#46678971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86021103-C-A

46678971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86021103-C-T

46678982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86021114-G-A

46679059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86021180-G-A

46679164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86021281-G-A

http://identifiers.org/hco/22/GRCh38#46679165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86021282-C-A

46679165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86021282-C-T

46679211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86021306-A-G

46679261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86021334-A-G

46679559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86021600-A-G

46679635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86021673-C-G

46679635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86021673-C-T

46679715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86021758-G-A

46679715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86021758-G-C

46679715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86021758-G-T

http://identifiers.org/hco/22/GRCh38#46679845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#86021883-C-A

46679845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86021883-C-T

46679867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86021894-T-C

46679895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86021912-T-A

46679996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86022031-G-A

46680464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86022391-G-A

46680561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29113
most severe consequence: intron variant
orthologous variants: 86022478-T-C