http://identifiers.org/hco/5/GRCh38#36877127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8473659-C-A

36877127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: 5 prime UTR variant
orthologous variants: 8473659-C-T

36877250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8473527-T-C

36877250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8473527-T-G

36877291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, undefined
orthologous variants: 8473486-T-C

36877291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, undefined
orthologous variants: 8473486-T-G

36877329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8473433-C-T

36877393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8473349-C-G

36878570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8472179-T-A

http://identifiers.org/hco/5/GRCh38#36878737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8472016-A-C

36879062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8471696-T-G

36879288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8471451-T-G

http://identifiers.org/hco/5/GRCh38#36879430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8471309-A-C

36881132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8469515-A-G

36881229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8469400-T-G

36881540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8469106-G-A

36881588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8469058-G-T

36881714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8468932-G-A

36881797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8468861-T-A

36882799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8467270-G-C

36883448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8466666-T-G

36883524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8466390-A-G

36886648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8464585-T-C

36887531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8463217-T-C

36887558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8463184-C-T

36889535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8462221-A-G

http://identifiers.org/hco/5/GRCh38#36889650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8462115-A-C

36889715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8461925-A-T

36890266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8461140-G-A

http://identifiers.org/hco/5/GRCh38#36890558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8460878-C-A

36890558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8460878-C-T

36890564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8460872-T-C

36890980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: -T-G

36890987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: -C-T

36891834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8458836-G-A

36893763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8457441-G-A

36894090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8457106-T-A

36894451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8456635-A-T

36897592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8453749-A-G

36898186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8453500-G-T

36898265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8453432-T-C

36898427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8453234-G-C

36898857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8452668-T-G

36898881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8452586-A-G

36898916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8452547-G-A

36898991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8452474-T-C

36899043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8452422-G-A

36899088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8452381-T-G

36899469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8452052-C-T

36899572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8451941-C-T

36911605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8441184-A-G

36911889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8440939-T-G

36911950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8440908-C-T

36911980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8440877-T-C

36911986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8440871-G-T

36912030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8440829-T-A

36912033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8440826-A-G

36912088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8440769-T-G

36913288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8439934-G-A

36913290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8439932-A-G

36913683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8439839-A-T

36914283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8439346-C-T

36922175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8437566-A-G

36922492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8437302-G-A

36922504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8437290-T-C

36922652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8437171-A-G

36922878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8436931-T-G

36922920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8436881-C-T

36922964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8436839-A-G

36922990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8436817-A-G

36923623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8436234-T-C

36924162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8435798-C-T

36924731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8435306-C-T

36925030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8435221-G-A

36925038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8435213-A-G

36925709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8434845-C-G

36926294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8434359-A-G

36926374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8434280-G-A

36926939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8433875-G-A

36926939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8433875-G-T

http://identifiers.org/hco/5/GRCh38#36927075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8433756-C-A

36927075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8433756-C-T

36927104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8433727-T-C

36927104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8433727-T-G

36928119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8428966-T-G

36931638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8428197-A-G

36931752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8428094-G-T

36932121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8427670-A-G

36932154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8427636-A-G

36932244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8427560-A-G

36932320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8427512-T-G

36932406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8427451-C-T

http://identifiers.org/hco/5/GRCh38#36932568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8427283-C-A

36932736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8427128-G-T

http://identifiers.org/hco/5/GRCh38#36932805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8427037-A-C

36932805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8427037-A-T

36933169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8426660-T-C

36937227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8423816-G-A

36937983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8421645-A-G

36938106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8421497-T-A

36938121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8421482-G-A

36938160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8421444-G-C

36938353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8421261-C-G

36940182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8420161-A-G

36941195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8416413-G-A

36941374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8415968-G-T

http://identifiers.org/hco/5/GRCh38#36944978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#8411748-A-C

36944978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, undefined
orthologous variants: 8411748-A-G

http://identifiers.org/hco/5/GRCh38#36945336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8411267-A-C

36945494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8411089-T-A

36945578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8410987-C-T

36945935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8410693-A-G

36946055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8410604-C-T

36948313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8408532-T-C

36948976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8408132-A-G

36949164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8407927-A-T

36949604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8407562-G-A

36951370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8406289-A-T

36951813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8405900-T-G

36951858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8405840-G-T

36952217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8405450-A-G

36952588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8405033-T-G

36953125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8404039-G-C

http://identifiers.org/hco/5/GRCh38#36953520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8403690-C-A

36954544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8402521-C-T

36954762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8402365-G-A

36954833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8402296-G-T

36954885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8402246-A-G

36955296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8401860-T-C

36955296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8401860-T-G

36955366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8401793-G-A

36955366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8401793-G-T

http://identifiers.org/hco/5/GRCh38#36955439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8401710-C-A

36955439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8401710-C-T

http://identifiers.org/hco/5/GRCh38#36955467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8401683-A-C

36955467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8401683-A-G

36955467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8401683-A-T

http://identifiers.org/hco/5/GRCh38#36955688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8401466-C-A

36955689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8401465-T-A

36955730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8401420-G-C

36957402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8399436-C-T

36957570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8399264-T-C

36958436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8398753-G-A

36958508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8398678-T-G

36958530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8398656-T-A

36960211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8397881-T-C

36960218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8397874-G-T

http://identifiers.org/hco/5/GRCh38#36961197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8396553-C-A

36961259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8396430-T-C

36961385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8396296-A-G

36961385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8396296-A-T

36961573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8396122-A-G

http://identifiers.org/hco/5/GRCh38#36961656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8396033-C-A

36961656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8396033-C-T

36961782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8395913-T-C

36962259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8395289-C-G

36966338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8392974-G-T

36966424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8392889-A-G

36966490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8392818-A-G

36966597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8392715-T-C

36970244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8391982-G-A

36970487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8391758-A-G

36970717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8391506-G-T

36971086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8391153-A-G

36971539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8390886-A-G

36971623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8390813-A-G

36971629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8390809-A-G

36971701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8390738-A-G

36971709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8390730-T-C

36971775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 8390663-C-G

36971820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 8390618-G-A

36971820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 8390618-G-T

36971948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8390491-G-A

36972032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8390407-A-G

36972324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8390209-G-A

36974005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8389659-G-C

36974114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8389540-T-A

36974231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8389388-A-G

36975680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8388819-T-A

36975680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8388819-T-G

36975733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8388786-T-C

36976321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8388203-G-T

36976437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8388087-G-A

36976437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8388087-G-T

36976478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8388066-T-A

http://identifiers.org/hco/5/GRCh38#36976623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8387993-A-C

36976623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8387993-A-T

36976642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8387978-T-C

36976747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8387876-A-G

36976747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8387876-A-T

36977172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8387268-A-G

36977474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8387049-T-C

36977528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8386967-A-T

36979783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8386764-A-G

36980164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8386017-A-G

36981694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8385052-G-T

36981699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8385047-T-C

36982110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8384449-A-G

36982604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8383238-A-G

36982738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8383120-G-C

http://identifiers.org/hco/5/GRCh38#36983004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8382871-A-C

36983245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8382641-G-A

36983377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8382532-C-G

36983427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8382477-G-A

36983427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8382477-G-T

36983622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8382286-A-G

36983668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8382239-G-A

36984514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8381432-T-C

36984906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8381063-G-A

36984906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8381063-G-T

36984989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8380980-G-C

36985177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8380792-G-A

36985671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8380304-G-A

36985683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8380292-G-A

36985683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8380292-G-C

36986926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8379034-T-C

36987040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8378955-A-G

36987327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8378773-T-C

36987416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8378680-A-G

36987515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8378586-T-C

36987577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8378537-C-G

36994817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8373821-A-G

36994817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8373821-A-T

36995111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8373527-G-A

36995111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8373527-G-T

36995143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8373495-T-C

36995181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8373462-T-C

36995297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8373384-T-A

36995302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8373379-G-A

http://identifiers.org/hco/5/GRCh38#36995379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8373322-C-A

36995379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8373322-C-T

36995546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8373204-T-A

http://identifiers.org/hco/5/GRCh38#36995551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8373199-C-A

36995551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8373199-C-T

36995878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8372898-T-A

http://identifiers.org/hco/5/GRCh38#36995890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8372887-C-A

36995890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8372887-C-T

36995974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8372802-C-G

36996955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8371859-C-G

36998396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8370502-T-A

36998741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8370276-T-C

36999579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8369345-T-C

36999678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8369249-G-A

36999988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8368917-G-A

37000293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8368633-A-G

37000474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 8368453-G-T

37000805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8368252-T-C

37000805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8368252-T-G

37000899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8368152-A-G

37001122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8367939-T-A

37001803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8367271-A-G

37001885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8367200-G-C

37002315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8366766-C-T

37002322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, undefined
orthologous variants: 8366759-C-T

37002554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8366537-T-A

37002635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8366466-T-G

37002821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8366279-T-C

http://identifiers.org/hco/5/GRCh38#37003138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8364871-C-A

37003138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8364871-C-T

37003204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8364809-T-C

37003239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8364774-A-G

37006313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8364616-A-G

37006643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8364193-A-G

http://identifiers.org/hco/5/GRCh38#37006655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8364179-A-C

37006661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8364173-G-A

37006661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8364173-G-T

37007162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8363386-T-G

37007513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8363025-T-A

37007532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8363010-T-A

37008104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8362474-T-C

37008225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8362358-A-G

37008361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8362261-T-C

37008375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8362247-T-C

37008486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8362146-G-T

37008559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8362037-G-A

37008559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8362037-G-T

37008820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8361786-A-G

37008903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8361712-A-T

37008965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8361660-C-T

37008984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8361642-C-T

37009004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8361622-T-C

37009064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8361579-A-G

http://identifiers.org/hco/5/GRCh38#37009090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8361556-C-A

37009090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8361556-C-G

37009263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8361116-T-G

37010002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8359886-C-T

37014367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8358619-C-T

37014445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8358517-C-G

37014596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8358377-A-G

http://identifiers.org/hco/5/GRCh38#37015958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8357413-A-C

37016010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8357387-A-G

37016072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: missense variant
orthologous variants: 8357325-C-T

http://identifiers.org/hco/5/GRCh38#37016120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8357277-C-A

37016176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8357221-A-G

37016682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8356702-C-G

37016682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8356702-C-T

37016709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8356679-A-G

http://identifiers.org/hco/5/GRCh38#37019347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8355219-A-C

37019719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8354829-A-G

http://identifiers.org/hco/5/GRCh38#37020182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8354390-A-C

37020182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8354390-A-G

37020231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8354337-C-G

37020305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8354266-T-C

37020647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: synonymous variant
orthologous variants: 8353953-C-T

37020705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8353896-A-G

37020764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8353843-T-C

37020933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8353687-C-T

37020985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8353643-T-C

37021709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8353526-T-G

37021999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8353274-T-C

37022528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8352744-C-T

37022760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8352531-G-C

http://identifiers.org/hco/5/GRCh38#37026009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8349246-C-A

37026340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8348928-G-A

37026510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8348800-C-T

37026564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8348750-C-G

http://identifiers.org/hco/5/GRCh38#37026785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8348641-C-A

37026878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8348575-T-A

http://identifiers.org/hco/5/GRCh38#37026879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8348574-C-A

37027167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8348246-T-C

37027222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8348225-G-T

37027241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8348210-A-G

37027314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8347987-A-G

37027572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8347708-T-C

http://identifiers.org/hco/5/GRCh38#37027986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8347638-A-C

37028032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8347339-T-C

37035641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8342577-A-G

37035834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8342406-A-G

http://identifiers.org/hco/5/GRCh38#37036018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8342217-C-A

37036368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8341935-T-A

37036368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8341935-T-C

37036368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8341935-T-G

37036523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8341783-A-G

37037495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8341188-C-G

37037593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8341097-G-A

http://identifiers.org/hco/5/GRCh38#37038831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8340377-C-A

37038831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8340377-C-T

37039168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8340018-C-T

37039385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8339827-A-G

37039402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8339810-T-A

37039928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8339405-T-A

37042005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8338645-T-A

37043872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, undefined
orthologous variants: 8338061-C-G

37044019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8337929-C-T

http://identifiers.org/hco/5/GRCh38#37044208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8337655-A-C

http://identifiers.org/hco/5/GRCh38#37044216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8337640-C-A

37044216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8337640-C-G

37044216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8337640-C-T

37044225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8337631-T-C

37044247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8337603-A-T

http://identifiers.org/hco/5/GRCh38#37044287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8337532-C-A

37044287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8337532-C-G

37044291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8337528-A-G

37044504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8337315-C-T

http://identifiers.org/hco/5/GRCh38#37044561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8337223-A-C

37044735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8337041-T-C

37045402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8336544-A-G

http://identifiers.org/hco/5/GRCh38#37045422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8336527-A-C

http://identifiers.org/hco/5/GRCh38#37045675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8336275-C-A

37045675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8336275-C-G

http://identifiers.org/hco/5/GRCh38#37045740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8336215-C-A

37045740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8336215-C-T

http://identifiers.org/hco/5/GRCh38#37045842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8336117-C-A

37046372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8335155-G-A

37046782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8334812-A-G

http://identifiers.org/hco/5/GRCh38#37046999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8334611-C-A

37047586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8334159-G-A

37047680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8333993-A-G

37047688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8333938-A-G

37048476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8333073-G-A

37048476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8333073-G-T

http://identifiers.org/hco/5/GRCh38#37048657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8332893-C-A

37048690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8332860-A-G

37048722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8332841-A-G

37048761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8332802-T-G

37048793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8332783-G-T

37048797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8332780-T-G

http://identifiers.org/hco/5/GRCh38#37048812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8332764-C-A

37048897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8332701-G-A

http://identifiers.org/hco/5/GRCh38#37048900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8332698-A-C

37048916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8332683-C-T

37049000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8332620-G-T

37049029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8332591-G-T

37049034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8332585-T-G

http://identifiers.org/hco/5/GRCh38#37049079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8332540-A-C

37049659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8331925-A-G

37049697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron variant
orthologous variants: 8331884-A-G

http://identifiers.org/hco/5/GRCh38#37051590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8331049-A-C

37051590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8331049-A-T

http://identifiers.org/hco/5/GRCh38#37051644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8331000-A-C

37051644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8331000-A-G

37051655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8330991-G-T

37051716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8330937-C-T

37051728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8330925-T-G

37051743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8330918-A-G

37051746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8330915-A-G

http://identifiers.org/hco/5/GRCh38#37051900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8330760-C-A

37051900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8330760-C-T

37051958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8330726-T-C

37051969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8330715-T-G

37052028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8330663-G-A

37052456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8330287-G-A

37052456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8330287-G-T

37053703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8329377-T-C

37053771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8329293-C-T

37054667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8328720-C-T

37054738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8328662-T-C

http://identifiers.org/hco/5/GRCh38#37054865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8328591-C-A

37054870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8328588-A-G

37056632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8326829-G-C

37057075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8326467-T-C

http://identifiers.org/hco/5/GRCh38#37057371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8326192-A-C

37057371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8326192-A-G

37057445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8326113-T-G

37058575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8325526-T-C

37058576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8325525-T-C

37058609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8325497-T-C

http://identifiers.org/hco/5/GRCh38#37058751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8325371-A-C

37058751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8325371-A-G

37058751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8325371-A-T

37059183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8324976-G-T

37060950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8322634-C-T

37061001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8322583-G-C

37061026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8322558-G-T

37061027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8322557-T-G

37063487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8322081-C-T

http://identifiers.org/hco/5/GRCh38#37063508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8322067-A-C

37063508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8322067-A-G

37063656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8321930-T-A

37063656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8321930-T-C

37064402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8321194-C-T

37065275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8320327-G-C

37065275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8320327-G-T

37065935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: 3 prime UTR variant
orthologous variants: 8319671-G-T

http://identifiers.org/hco/5/GRCh38#37066401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28862
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#8319317-A-C