54846735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76474395-T-C

54846888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76474308-G-A

54846920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76474302-G-A

54846920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76474302-G-T

54846965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76474289-G-C

54846965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76474289-G-T

54847227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: 76474119-A-G

54847261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76474094-G-A

54847342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76474042-G-T

54847519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76473908-C-G

54848040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76473442-G-A

http://identifiers.org/hco/6/GRCh38#54848247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76473290-C-A

http://identifiers.org/hco/6/GRCh38#54848275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#76473262-C-A

54848288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: 76473249-G-A

54848315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: 76473222-C-T

54848814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76472442-T-C

http://identifiers.org/hco/6/GRCh38#54848921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76472335-A-C

54848944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76472312-A-G

54849199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76472077-T-G

54849700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76471038-C-G

54849935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76470812-T-C

54849935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76470812-T-G

54849937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76470810-C-T

http://identifiers.org/hco/6/GRCh38#54850114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76470645-A-C

54850336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76470468-G-C

http://identifiers.org/hco/6/GRCh38#54850342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76470462-C-A

54850402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76470405-T-C

54850558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76470249-C-T

54850630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76470173-A-G

54856226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76468142-T-C

54856302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76468070-T-C

54856573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76467893-A-T

54857062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76467357-T-A

54857062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76467357-T-C

54857215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76467110-A-G

54857400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76466941-T-G

54857603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76466787-T-C

54857754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76466688-T-G

54857795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76466643-T-C

54857847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76466593-G-A

54857985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76466464-C-T

54858004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76466446-G-A

54858330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76466145-T-C

54858635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76465003-A-G

54858700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76464945-A-T

54858979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76464718-G-A

54859772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: -A-T

54859928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: -T-G

http://identifiers.org/hco/6/GRCh38#54859942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: -A-C

54863292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76460760-A-G

54863413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76460639-A-G

54863464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76460584-A-G

54863540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76460527-G-A

54863540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76460527-G-T

54863562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76460515-C-G

54863851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76460419-G-A

http://identifiers.org/hco/6/GRCh38#54863922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76460344-C-A

54864005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76460209-G-A

54864086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76460125-G-A

54864168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76460041-C-T

54864296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76459906-A-T

54864311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76459891-A-G

54868196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76455666-G-A

54868257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76455607-G-A

54868327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76455544-G-A

54868334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76455537-T-G

54868520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76455354-A-T

http://identifiers.org/hco/6/GRCh38#54869454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76453931-C-A

54869454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76453931-C-T

http://identifiers.org/hco/6/GRCh38#54869483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76453902-C-A

54869483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76453902-C-T

54869630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76453782-G-A

54869790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76453605-A-G

54869836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76453561-T-C

54869837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76453560-T-G

54869853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76453544-C-T

54869915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76453448-T-C

54869956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76453389-C-G

http://identifiers.org/hco/6/GRCh38#54870154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76453153-C-A

54870154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76453153-C-G

54870154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76453153-C-T

54870228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: 5 prime UTR variant
orthologous variants: 76453081-T-C

54870301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76453009-T-C

54870331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: stop gained
orthologous variants: 76452979-C-T

54870376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76452934-C-G

54870574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76452736-T-C

http://identifiers.org/hco/6/GRCh38#54870725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76452585-A-C

54870725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76452585-A-G

54870725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76452585-A-T

54870731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76452581-G-A

http://identifiers.org/hco/6/GRCh38#54871127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76452001-C-A

54871340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76451793-T-G

54871445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76451652-G-A

54871526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76451587-C-G

54871929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76451375-T-C

54872503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76450903-G-T

54872770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76450712-G-A

54872971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76450533-G-A

54873641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76449804-T-C

54873726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76449711-G-T

54873785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: 76449652-A-G

54873932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76449507-A-G

54874006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: 76449434-A-G

54874678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: 76448727-A-G

http://identifiers.org/hco/6/GRCh38#54874715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#76448694-C-A

54874754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76448640-G-A

54874970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: 76448431-T-C

http://identifiers.org/hco/6/GRCh38#54875307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76448143-C-A

http://identifiers.org/hco/6/GRCh38#54877034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76445723-C-A

54877059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76445696-C-T

http://identifiers.org/hco/6/GRCh38#54880827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76444458-C-A

54881341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76443900-T-C

54881455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76443772-T-G

http://identifiers.org/hco/6/GRCh38#54881569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76443631-A-C

54889286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76441891-A-T

54890288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76440823-C-T

54890610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76440108-A-G

54892807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76440086-A-G

54892807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76440086-A-T

54892868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76440026-G-A

54892886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: 76440008-G-A

54892886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: 76440008-G-T

54893227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76439696-A-G

54893244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76439679-T-C

54893271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76439652-A-G

54893326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76439607-C-T

http://identifiers.org/hco/6/GRCh38#54893397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76439530-C-A

54893451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76439476-A-G

54893608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76439367-A-G

54893681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76439295-A-T

54894049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76439261-A-G

54894086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76439224-T-C

54894393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76438987-G-A

54894393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76438987-G-C

54894757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76438630-A-G

54894862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76438532-C-T

54894880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76438514-G-A

54895112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76438227-T-C

54895152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76438156-T-C

54895243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76438059-T-C

54895250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76438051-T-C

54895307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76437994-C-G

54895455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76437863-C-T

54896781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76437595-C-T

54896799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76437578-A-G

54896997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76437377-T-C

54897360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76436999-T-G

54897421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76436946-C-T

http://identifiers.org/hco/6/GRCh38#54897467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76436900-C-A

54897467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76436900-C-T

54897499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76436870-A-T

54897656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76436724-T-A

54897924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76436523-C-G

54897924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76436523-C-T

http://identifiers.org/hco/6/GRCh38#54897926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76436521-A-C

54898141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76436303-T-C

54898392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76436078-G-A

54898451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76436020-G-C

54898598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76435885-A-G

54898688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76435797-T-C

54898721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76435764-C-T

54898796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76435689-G-A

http://identifiers.org/hco/6/GRCh38#54900357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76433591-C-A

54900357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76433591-C-T

54900675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76433216-T-C

54900730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76433148-C-T

54900739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76433130-T-G

54901016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76432844-T-C

54901182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76432699-T-C

54901185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76432696-T-A

54901336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76432656-T-A

54901451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76432601-A-G

54901559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76432478-T-C

54901672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76432387-T-A

54901945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76432143-A-G

54902096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76432022-T-G

54902105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76432013-T-G

54902110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76432008-T-C

54904049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76430507-G-T

54904154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76430401-T-G

54904267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76430290-T-C

54904315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76430241-C-T

54904478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76429637-T-A

54904550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76429571-A-G

http://identifiers.org/hco/6/GRCh38#54904624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76429516-C-A

54905119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76429151-A-G

54905331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76428963-T-C

54905392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76428901-A-G

54905783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76428217-A-G

54906071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76427913-A-G

54906945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76427273-A-G

54907659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76425412-T-C

http://identifiers.org/hco/6/GRCh38#54907978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76425101-A-C

54907989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76425090-A-G

54910186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76423247-C-T

54910264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76423159-C-G

54910275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76423144-G-A

54910276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76423143-A-T

54910314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76423105-T-C

54910378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76423048-A-G

54910507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76422914-G-A

54910510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76422911-G-A

54910541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76422880-A-G

http://identifiers.org/hco/6/GRCh38#54910731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76422691-A-C

54910812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76422610-T-C

54910812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76422610-T-G

54910949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76422478-C-T

54911062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76422374-C-T

54911190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76422280-T-C

54911308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76422179-A-G

54911540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76422019-T-G

54911626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76421941-T-C

54911707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76421856-C-T

54911897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76421668-A-G

54912093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76421483-C-G

54912270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76421312-T-C

http://identifiers.org/hco/6/GRCh38#54912429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76421195-A-C

http://identifiers.org/hco/6/GRCh38#54912649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76421008-A-C

54912649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76421008-A-G

54912669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76420988-A-T

54912778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76420882-T-G

54917161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76420713-C-G

54917367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76420570-G-C

54917400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76420534-G-C

54917410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76420524-A-T

http://identifiers.org/hco/6/GRCh38#54917495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76420456-A-C

54917694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76420293-C-T

54917866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76420184-C-T

54917988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76420069-G-A

54918045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76420018-G-A

54918860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76414380-C-T

54918861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76414379-T-C

54919082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76414151-G-A

54919089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76414145-T-G

54919492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76413971-T-A

54919556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76413914-A-G

http://identifiers.org/hco/6/GRCh38#54919668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76413817-A-C

54919857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76413649-G-A

54919866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76413640-A-G

54920612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76413074-A-G

http://identifiers.org/hco/6/GRCh38#54920775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76412517-A-C

54920795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76412500-G-A

54922235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76411921-G-A

http://identifiers.org/hco/6/GRCh38#54922448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76411714-C-A

54922448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76411714-C-T

54922494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76411673-A-G

54922494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76411673-A-T

54922650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76411525-T-C

54926070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76410741-C-T

54926127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76410685-T-G

54926227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76410602-A-G

54926232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76410597-A-G

54926278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76410551-A-T

54926649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76410178-G-A

54926649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76410178-G-T

54926708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76410142-A-G

54926732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76410125-T-C

54926784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76410086-G-A

54926827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76410043-G-A

54926881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76410005-G-A

http://identifiers.org/hco/6/GRCh38#54927399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76409611-C-A

54927399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76409611-C-G

54927399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76409611-C-T

http://identifiers.org/hco/6/GRCh38#54927409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76409601-A-C

54927409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76409601-A-G

54927409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76409601-A-T

54927410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76409600-T-A

54927410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76409600-T-G

http://identifiers.org/hco/6/GRCh38#54927423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76409589-A-C

54927423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76409589-A-T

54927437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76409575-T-C

54927437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76409575-T-G

http://identifiers.org/hco/6/GRCh38#54927472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76409543-C-A

54927472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76409543-C-T

54927512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76409509-T-C

54927532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76409489-G-A

54927642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76409379-T-A

54927642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76409379-T-C

54927673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76409348-T-C

54927707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76409314-A-T

http://identifiers.org/hco/6/GRCh38#54927714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76409307-C-A

54927714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76409307-C-T

54928151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76408291-A-G

http://identifiers.org/hco/6/GRCh38#54928275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76408171-A-C

54928275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76408171-A-G

54928316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76408133-C-T

54928397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76408076-T-C

54928595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76407702-A-G

http://identifiers.org/hco/6/GRCh38#54928603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76407694-C-A

54928779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76407519-T-A

54928863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76407448-A-G

54928975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76407313-T-C

54929410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: 76406015-A-G

54929568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: 76405685-T-C

54929702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: 76405560-C-T

54929724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: 76405538-A-G

54929824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: 76405411-A-G

54929998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76405235-C-T

54930105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76405115-T-C

54930113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76405099-A-G

54930132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76405080-T-C

54930146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76405066-G-A

54930146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76405066-G-T

54930535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76404390-T-A

54931121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76404340-T-C

http://identifiers.org/hco/6/GRCh38#54931217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76404246-C-A

http://identifiers.org/hco/6/GRCh38#54931272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76404214-C-A

54931389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76404131-C-T

54931682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76403828-T-C

54931759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76403754-A-G

54931957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76403594-G-T

54935540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76402916-G-A

54935661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: 76402795-A-G

54935835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: 76402633-G-C

54935935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: 76402464-G-A

54936017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: 76402381-G-A

54936218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron_variant, undefined
orthologous variants: 76402179-A-T

54936610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76401869-T-G

54936951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76401445-T-G

54936995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76401403-G-T

54937034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76401373-T-C

54937126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76401292-A-G

54937203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76401215-C-T

54937280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76401158-T-C

54937327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76401108-G-C

54937687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76400766-C-T

54937688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76400765-G-A

54937688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76400765-G-C

54937697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76400756-G-A

54937851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76400611-G-A

54939591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76400481-A-G

54939613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76400462-A-G

54939618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76400457-A-G

54939618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76400457-A-T

54939642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76400433-T-A

54939642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: intron variant
orthologous variants: 76400433-T-C

54939850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: synonymous variant
orthologous variants: 76400221-G-A

54939896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76400175-T-A

54939914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76400157-T-A

54940010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76400061-G-A

54940010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: stop gained
orthologous variants: 76400061-G-T

http://identifiers.org/hco/6/GRCh38#54940088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76399983-C-A

54940088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76399983-C-T

54940151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76399920-C-T

54940236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76399835-G-T

54940262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76399809-G-A

54940262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76399809-G-C

54940308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76399763-A-G

54940480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: synonymous variant
orthologous variants: 76399591-T-C

54940508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76399563-G-A

54940769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76399302-C-T

http://identifiers.org/hco/6/GRCh38#54940958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76399113-C-A

54940958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: stop gained
orthologous variants: 76399113-C-T

54940992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76399079-A-G

54941144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76398927-A-G

54941145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76398926-C-T

54941156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76398915-T-A

54941585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76398483-C-G

54941586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76398482-C-T

54941612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76398456-G-T

54941741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: synonymous variant
orthologous variants: 76398327-C-T

54941763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76398305-G-A

54941763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76398305-G-T

54941892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76398176-G-C

54941900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: 76398168-C-T

http://identifiers.org/hco/6/GRCh38#54941906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#76398162-C-A

54941960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: stop gained
orthologous variants: 76398108-C-T

54942456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: 3 prime UTR variant
orthologous variants: 76397608-C-T

54943035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: 3 prime UTR variant
orthologous variants: 76397159-T-C

54943084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: 3 prime UTR variant
orthologous variants: 76397122-G-T

54943475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 76396898-T-G

54944060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 76395545-A-T

54944386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 76395234-T-C

54944435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 76395200-G-A

54944435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21357
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 76395200-G-T