61054226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9057801-G-A

61054344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, undefined
orthologous variants: 9057912-G-A

61054398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9057963-T-A

61055838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, undefined
orthologous variants: 9059032-T-C

61055932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, undefined
orthologous variants: 9059125-C-T

61056050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9059241-T-C

61056166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9059315-G-A

61056234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9059378-T-C

61056371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9059482-C-G

61056511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9059857-A-T

61056536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9059881-C-T

http://identifiers.org/hco/8/GRCh38#61056581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9060011-C-A

http://identifiers.org/hco/8/GRCh38#61056631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9060063-C-A

http://identifiers.org/hco/8/GRCh38#61056865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9060290-C-A

61057195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9060607-C-T

http://identifiers.org/hco/8/GRCh38#61057546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9061595-A-C

61057654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9061702-G-C

61057729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9061776-G-A

61058244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9062255-G-A

61058353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9062366-G-T

61060406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9064835-C-G

61060495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9064919-G-A

61060561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9064983-C-G

61060682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9066016-T-C

61060857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9066181-A-T

http://identifiers.org/hco/8/GRCh38#61060867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9066192-C-A

61061015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9066244-A-G

61061069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9066302-T-C

61061224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9066440-A-G

61061229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9066445-C-T

61061768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9066980-G-A

61061840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9067061-G-A

61061930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9067141-T-A

61061979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9067190-G-A

61062037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9067248-G-A

61062050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9067261-T-C

61062844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9067916-G-A

61063148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9068174-G-A

61063256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9068277-G-A

http://identifiers.org/hco/8/GRCh38#61063311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9068294-A-C

61063311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9068294-A-G

61063431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9068404-G-C

http://identifiers.org/hco/8/GRCh38#61066577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9072841-C-A

61066613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9072882-C-T

http://identifiers.org/hco/8/GRCh38#61066804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9073069-A-C

http://identifiers.org/hco/8/GRCh38#61067038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9073276-C-A

61067070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9073305-C-T

61067212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9073433-T-C

61067233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9073454-G-C

61067287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9073517-G-A

61068401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9073757-A-G

61068810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9074130-C-G

61068819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9074139-C-T

61068832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9074152-A-G

http://identifiers.org/hco/8/GRCh38#61070041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9074713-C-A

61070158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9074813-T-C

61070267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9074904-G-A

http://identifiers.org/hco/8/GRCh38#61070268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9074905-C-A

61070356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9074988-C-T

http://identifiers.org/hco/8/GRCh38#61070392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9075030-C-A

61070392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9075030-C-T

http://identifiers.org/hco/8/GRCh38#61070513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9075154-C-A

61070513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9075154-C-T

http://identifiers.org/hco/8/GRCh38#61070514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9075155-C-A

61070528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9075169-G-A

61071593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9075588-A-G

61071677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9075663-T-C

61071728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9075702-A-G

61071776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9075750-C-T

61072513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9077921-A-G

61074589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9079001-C-T

61074833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9079620-A-G

http://identifiers.org/hco/8/GRCh38#61074855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9079642-C-A

61074855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9079642-C-T

61075352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9080127-C-T

http://identifiers.org/hco/8/GRCh38#61075382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9080158-A-C

http://identifiers.org/hco/8/GRCh38#61075386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9080162-C-A

http://identifiers.org/hco/8/GRCh38#61075607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9080391-C-A

61075607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9080391-C-T

61075609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9080393-C-T

61075623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9080407-T-C

61075788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9080473-C-T

61075978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9080651-C-T

61076047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9080716-G-T

61076133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9080792-A-G

61076565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9081117-T-C

61076636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9081188-C-T

61076944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9081459-G-C

http://identifiers.org/hco/8/GRCh38#61077776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9081719-C-A

61078574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9082498-C-G

61078792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9082696-C-T

61078981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9083243-G-A

61079232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9083485-C-T

61079373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9083625-G-A

http://identifiers.org/hco/8/GRCh38#61079640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9083883-C-A

61079652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9083895-C-G

http://identifiers.org/hco/8/GRCh38#61079773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9084017-A-C

http://identifiers.org/hco/8/GRCh38#61079799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9084041-A-C

61079807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9084049-A-G

61079829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9084070-G-A

61079847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9084084-C-G

61079847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9084084-C-T

61080024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9085467-G-A

61080395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9085928-G-A

61080702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9086208-G-A

61080702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9086208-G-C

http://identifiers.org/hco/8/GRCh38#61080947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9086421-C-A

61086335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9089257-T-G

61086768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9089667-G-A

61086823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9089718-C-T

61086843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9089738-C-G

61086843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9089738-C-T

61087368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9090170-C-T

61089319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9091994-C-G

61089988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9092247-T-C

61090114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9092366-T-C

61090281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9092488-C-T

61090475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9092679-T-C

61091725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9092832-C-T

61091785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9092901-A-G

61091808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9092924-A-G

61091953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9093048-T-A

61091959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9093054-A-T

61092000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9093128-C-T

http://identifiers.org/hco/8/GRCh38#61092298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9093351-A-C

61092343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9093387-C-T

http://identifiers.org/hco/8/GRCh38#61092391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9093413-A-C

61092397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9093419-G-A

61092477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9093488-C-T

http://identifiers.org/hco/8/GRCh38#61092699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9093691-C-A

61092699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9093691-C-G

61092767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9093757-A-G

61092854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9093802-C-T

61092952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9093932-G-A

http://identifiers.org/hco/8/GRCh38#61093087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9094035-C-A

61093087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9094035-C-G

61093162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9094110-G-C

61093186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9094135-G-A

61093482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9094406-G-A

http://identifiers.org/hco/8/GRCh38#61093494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9094421-A-C

http://identifiers.org/hco/8/GRCh38#61093497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9094424-C-A

61093497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9094424-C-T

61093594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9094521-G-A

61093758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9094692-T-C

61093758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9094692-T-G

61093818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9094757-G-A

61093818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9094757-G-T

61093872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9094811-G-A

61093906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9094845-G-A

61093950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9094889-A-G

61093972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9094910-G-A

61094593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9095558-T-C

61094624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9095579-T-C

61094753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9095708-C-G

61095071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9095994-G-A

61095164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9096085-G-A

61095213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9096130-T-G

http://identifiers.org/hco/8/GRCh38#61095311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9096271-C-A

http://identifiers.org/hco/8/GRCh38#61095423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9096384-C-A

61095783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9096733-A-G

61095891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9096861-C-T

http://identifiers.org/hco/8/GRCh38#61096288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#9097258-A-C

61096336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9097297-T-C

61096550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9097452-T-C

61096571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9097474-G-A

61097481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9098066-C-G

61097481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9098066-C-T

61097538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9098123-G-A

61097577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9098161-C-T

61097583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9098167-A-T

61097910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9098505-C-T

61097930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9098523-G-A

61098266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9098588-T-A

61098621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9098913-G-A

61098673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9098954-A-G

http://identifiers.org/hco/8/GRCh38#61098918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9099190-C-A

61098918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9099190-C-T

61098944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9099215-T-G

61099237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9099492-C-G

61099262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9099517-A-G

61099262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9099517-A-T

61099355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9099592-A-G

61099380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9099617-C-T

61099670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9099894-T-C

http://identifiers.org/hco/8/GRCh38#61099820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9100032-C-A

61099882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9100094-A-G

61099946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9100158-C-T

61101823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9100537-G-T

61101892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9100611-T-C

61102162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9100875-C-T

61102223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9100937-A-T

61102241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9100951-T-A

http://identifiers.org/hco/8/GRCh38#61102614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9101568-C-A

61102685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9101641-C-T

61102686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9101642-A-G

61103110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9103660-A-G

61103118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9103668-C-G

61103170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9103721-T-C

61104002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9104512-A-G

61104099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9104587-A-G

61104161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9104648-G-A

61104204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9104680-T-C

61106274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9107133-C-G

61106275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9107134-A-T

61106310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9107176-C-T

61106427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9107289-G-A

61106512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9107319-G-A

61106520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9107327-G-C

61107295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9108049-T-A

61107400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9108154-A-G

61107585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9108318-C-T

61107713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9108448-C-T

61107890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9108611-C-T

61108113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9108700-C-T

61108565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9109140-T-G

http://identifiers.org/hco/8/GRCh38#61108866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9109417-C-A

61108866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9109417-C-T

61108920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9109460-C-G

61108946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9109482-G-C

61108962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9109498-C-T

61109063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9109575-A-G

61109208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9109657-A-G

61109475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9109876-T-A

61109511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9109920-T-C

61114010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9113118-C-T

61114395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9113494-G-C

61114396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9113495-C-T

http://identifiers.org/hco/8/GRCh38#61114413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9113513-C-A

61114413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9113513-C-T

61114439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9113532-C-T

61114461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9113572-C-T

61114464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9113575-A-G

61114545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9113702-C-T

61114799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9113938-T-C

61114868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9113993-A-T

61114872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9113997-T-C

61114892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9114017-T-A

61114944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9114064-G-A

http://identifiers.org/hco/8/GRCh38#61115224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9114331-C-A

61115242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9114354-C-G

61115242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9114354-C-T

61115304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9114416-A-T

61121415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9114445-T-G

61121475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9114515-G-A

61121475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9114515-G-C

61121494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9114534-G-A

61121517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9114556-T-C

61121606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9114631-A-G

61121674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9114688-T-G

61121733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9114744-G-A

61121756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9114763-A-T

61121771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9114778-C-G

http://identifiers.org/hco/8/GRCh38#61122013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9115051-C-A

61122093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9115316-A-G

61122207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9115511-G-A

61122207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9115511-G-C

61122287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9115586-G-A

61122313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9115612-A-T

61122517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9115796-C-G

61122517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9115796-C-T

http://identifiers.org/hco/8/GRCh38#61122930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9116251-C-A

61123453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: -T-C

61123453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: -T-G

61123603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: -T-C

61124152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9117846-T-C

61124566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9118185-A-G

61125181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9118529-G-T

61125224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, undefined
orthologous variants: 9118572-C-T

61125486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, undefined
orthologous variants: 9118790-T-A

61125569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, undefined
orthologous variants: 9118884-T-C

61125790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9119109-G-T

61125990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9119307-A-G

61125990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9119307-A-T

61126113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, undefined
orthologous variants: 9119399-G-A

61126750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9121445-C-T

61127071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9121754-G-A

61127081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9121764-G-T

61127664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9121997-A-G

61127787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9122108-C-G

61127787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9122108-C-T

61127866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9122183-C-T

61128060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9122369-G-T

http://identifiers.org/hco/8/GRCh38#61128410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9122839-C-A

61128613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9123125-C-T

61128660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9123158-C-T

61128941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9123419-T-A

61128941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9123419-T-G

61129296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9123795-G-A

61129626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9124228-A-G

61129754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9124380-T-G

61130332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9125951-C-T

61130522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9126114-G-A

61130726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9126334-T-A

61130775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9126373-G-A

61130944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9126521-C-T

http://identifiers.org/hco/8/GRCh38#61131035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9126619-C-A

61131099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9126680-G-C

61131317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9126909-T-C

61131437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9127008-G-A

61131440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9127011-G-A

61131504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9127087-G-C

61131506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9127089-C-G

61131506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9127089-C-T

61135997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9131775-A-T

61136024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9131802-G-A

61136315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9132058-T-C

61137669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9133190-T-G

61137924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9133420-G-A

61137924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9133420-G-C

61137972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9133462-G-A

61137988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9133479-C-T

http://identifiers.org/hco/8/GRCh38#61138111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9133626-A-C

61138145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9133659-T-A

61138953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9135736-A-G

61139191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, undefined
orthologous variants: 9135957-T-C

61139199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, undefined
orthologous variants: 9135964-G-C

61139284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9136050-T-A

61139517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9136301-T-C

61139526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9136310-C-T

61139688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, undefined
orthologous variants: 9136516-T-C

61139718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, undefined
orthologous variants: 9136539-G-A

61140431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9137009-G-A

61140535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9137098-A-T

61141150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9137332-T-C

61141176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9137357-G-A

61141817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9137913-G-T

61141825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9137921-C-T

61141827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9137923-T-A

61141846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9137937-G-A

http://identifiers.org/hco/8/GRCh38#61141904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9137990-C-A

61141927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9138013-T-C

61141928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9138014-C-G

61142497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9138224-G-A

61142822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9138482-G-A

61142822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9138482-G-C

61145421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9139644-A-T

61145428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9139651-G-A

61145453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9139676-A-G

61147247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9139980-G-A

61147337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9140069-T-A

61147405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9140137-T-C

61147467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9140194-G-A

61147467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9140194-G-T

61149783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9141362-G-A

61149952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9141534-A-G

61149954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9141536-G-T

61149978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9141561-G-C

61150039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9141611-C-T

61151198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9144536-G-T

61153290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9147640-G-C

61153363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9147713-G-A

61153363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9147713-G-T

61153532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, undefined
orthologous variants: 9147882-T-C

61153596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, undefined
orthologous variants: 9147952-C-T

61153613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9147969-C-T

61153653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9148009-A-G

61153653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9148009-A-T

61153744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9148098-C-T

61153820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, undefined
orthologous variants: 9148176-T-C

61153828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, undefined
orthologous variants: 9148184-A-G

61153852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, undefined
orthologous variants: 9148210-A-G

61154290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9148612-G-A

61156642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9149504-T-C

61159382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9161613-G-C

61159411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9161642-C-T

61159439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9161670-C-T

61159677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9161902-T-C

61159678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9161903-G-A

61159678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9161903-G-T

61159691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9161916-T-A

61159732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9161958-C-G

61159732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9161958-C-T

61159877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9162083-C-G

61160166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9162556-A-T

61170045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9169761-G-A

61170351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9170005-A-G

61170407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9170053-G-A

61170407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9170053-G-C

61170439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9170086-C-T

http://identifiers.org/hco/8/GRCh38#61170515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9170146-A-C

61170526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9170157-T-C

61170712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9170257-C-T

61170777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9170309-A-G

61170915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9170410-A-T

61170976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9170464-T-C

61171008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9170480-C-T

61171018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9170490-T-G

61171108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9170552-T-C

61171232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9170693-G-A

61171346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9170795-A-G

http://identifiers.org/hco/8/GRCh38#61171491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9170967-C-A

61171575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9171044-C-T

61171640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9171085-T-C

61171693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9171138-G-A

61171831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9171277-A-G

61171839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9171285-G-A

61171883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9171328-T-C

http://identifiers.org/hco/8/GRCh38#61171963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9171392-C-A

61172012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9171440-T-C

61173756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9176066-G-A

61173756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9176066-G-C

61173947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9176247-T-C

61174044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9176337-G-A

61174536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9176692-A-T

61174608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9176749-T-G

61174742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9176886-G-C

61174783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9176921-A-G

61174849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9176986-G-A

http://identifiers.org/hco/8/GRCh38#61174922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9178443-C-A

61174922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9178443-C-G

61174922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9178443-C-T

http://identifiers.org/hco/8/GRCh38#61174931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9178452-C-A

61174931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9178452-C-G

61174931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9178452-C-T

61174953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9178473-C-T

61174957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9178477-G-T

61174989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9178509-C-T

61175065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9178588-T-G

61175221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9178747-A-T

http://identifiers.org/hco/8/GRCh38#61175409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9178916-C-A

61175470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9178971-G-A

61175554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9179054-G-A

61175592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9180965-G-C

61175594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9180967-G-T

http://identifiers.org/hco/8/GRCh38#61175603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9180976-A-C

61175638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9181016-C-G

61175722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9181097-G-A

61175765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9181137-T-C

61175830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9181210-C-G

61176289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9181658-G-C

61176359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9181729-C-T

61176392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9181766-C-T

61176440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9181819-G-A

61183528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9182236-G-A

61183890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9182559-T-C

61183898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9182567-G-A

61183917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9182588-G-A

61183994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9182665-T-A

61184018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9182849-T-C

61184039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9182872-T-C

http://identifiers.org/hco/8/GRCh38#61184178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9183022-A-C

61184259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9183109-T-C

61184311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9183156-A-T

61184329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9183174-A-G

61184381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9183219-G-A

61184430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9183267-T-C

61184566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9183384-T-C

61184675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9183470-C-T

http://identifiers.org/hco/8/GRCh38#61184707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9183495-A-C

61185004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9183790-G-A

61185073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9183856-A-G

61185461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9183919-C-T

61185558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9184017-A-G

61185565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9184024-C-T

61185578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9184037-A-G

61185590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9184049-A-T

61185719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9184189-G-T

61186130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9184629-G-T

61186313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9184807-T-C

61186718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9185098-T-C

61186845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9185213-G-A

61186961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9185315-G-A

61187017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9185343-A-G

61187100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9185419-G-A

61187178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9185506-T-C

61187213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9185540-A-G

61187273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9185599-T-C

61187355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9185757-C-T

61187571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9185947-A-G

61187580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9185956-A-G

61187950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9186172-T-C

61188180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9186394-A-T

61188576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9186899-G-T

61188766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9187102-G-A

http://identifiers.org/hco/8/GRCh38#61204624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9193103-A-C

61204902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9193361-T-C

61205626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9195193-G-T

61205648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9195215-T-C

61206105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9195841-C-T

61206121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9195856-T-G

http://identifiers.org/hco/8/GRCh38#61206890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9196565-A-C

61207008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9196669-C-T

61207055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9196707-C-G

61207055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9196707-C-T

61207056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9196708-G-A

http://identifiers.org/hco/8/GRCh38#61207808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9199984-C-A

http://identifiers.org/hco/8/GRCh38#61208069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9200277-C-A

61214711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9201959-C-G

61214725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9201973-G-A

61215055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9202296-T-C

61215163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9202413-T-A

61215181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9202431-A-G

61215356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9202565-G-C

61215424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9202625-T-G

61215645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9202863-T-C

http://identifiers.org/hco/8/GRCh38#61216019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9204879-C-A

61216102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9204959-G-A

61216277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9205108-G-C

61216392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9205227-C-T

61216451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9205276-G-C

61216541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9205366-G-A

61216571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9205398-A-G

http://identifiers.org/hco/8/GRCh38#61216584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9205410-C-A

61216644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9205472-G-A

61216829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9205619-G-T

61217000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9205764-C-T

61225586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9208563-T-C

61225639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9208612-T-C

61225663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9208638-C-T

http://identifiers.org/hco/8/GRCh38#61225857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9208836-C-A

61225857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9208836-C-G

61226158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9209189-A-G

61226422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9209595-T-A

61226422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9209595-T-C

61226486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9209665-C-T

61226489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9209668-T-C

61226574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9209875-C-T

61226647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9210113-C-T

61226650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9210116-G-A

61226723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9210184-A-G

61226725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9210186-C-T

61226773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9210243-A-G

61226824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9210306-C-T

61226825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9210307-G-A

61227053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9210510-G-C

61227069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9210526-T-C

61227092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9210551-G-A

61227132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9210590-A-G

61227294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9210760-C-T

61227317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9210783-G-T

61227319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9210785-G-A

61227319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9210785-G-T

61227322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9210788-C-T

61227360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9210822-T-C

http://identifiers.org/hco/8/GRCh38#61227373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9210835-C-A

http://identifiers.org/hco/8/GRCh38#61227575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9211013-A-C

61227724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9211149-T-G

61227897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9211305-T-C

61227908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9211316-G-A

61227986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9211392-T-C

61228156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9211530-C-T

http://identifiers.org/hco/8/GRCh38#61228183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9211550-A-C

61228184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9211551-A-G

http://identifiers.org/hco/8/GRCh38#61228324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9211663-C-A

61228693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9211917-C-T

61228910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9212088-A-G

61228926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9212104-G-T

61229142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9213293-T-A

61229437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9213582-A-G

http://identifiers.org/hco/8/GRCh38#61229522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9213653-C-A

61229882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9214317-C-G

61229882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9214317-C-T

61229891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9214326-A-T

61230213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9215351-G-A

61230234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9215372-C-G

61230350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9215434-C-G

61230359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9215443-G-T

http://identifiers.org/hco/8/GRCh38#61230432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9215511-A-C

61230442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9215521-T-G

61230459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9215538-G-C

61230564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9215621-T-G

http://identifiers.org/hco/8/GRCh38#61230687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9215743-A-C

61230853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9215907-T-G

61232840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9216288-C-T

61232882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9216324-A-G

61234443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9218987-C-T

61234457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9219001-C-T

61234481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9219023-A-G

61234488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9219028-C-T

61234540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9219082-T-C

61234562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9219097-C-G

61234564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9219099-C-T

61234573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9219108-G-A

61234573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9219108-G-T

61234586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9219121-G-A

61234751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9219310-C-T

61235197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9219756-C-T

http://identifiers.org/hco/8/GRCh38#61235236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9219793-C-A

61235299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9219833-C-T

61235351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9219903-T-C

61235414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9219966-G-A

61235462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9220003-G-T

61235544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9220082-T-C

61235841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9220367-C-T

61235845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9220371-G-T

61235931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9220457-A-G

61235931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9220457-A-T

61236164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9220678-T-C

61236280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9220782-G-A

61236284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9220788-C-T

61236329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9220822-G-A

http://identifiers.org/hco/8/GRCh38#61236431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9220925-A-C

61236576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9221060-C-T

http://identifiers.org/hco/8/GRCh38#61236769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9221242-A-C

61236769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9221242-A-G

61236778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9221251-T-A

61236864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9221344-C-T

61236921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9221404-A-G

61236927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9221410-G-A

61237011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9221504-C-T

61237083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9221884-G-C

61237103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9221904-G-A

61238018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9224069-G-T

http://identifiers.org/hco/8/GRCh38#61238110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9224151-A-C

61238110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9224151-A-T

61238111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9224152-T-C

61238259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9224281-C-T

61238591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: -A-G

61238718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: -T-C

61238763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: -A-G

http://identifiers.org/hco/8/GRCh38#61238776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: -A-C

61238791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: -T-A

61238791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: -T-C

61238816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: -T-A

61238832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: -C-T

61238846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: -T-C

61239064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: -C-T

61256791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9234178-T-C

http://identifiers.org/hco/8/GRCh38#61256800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9234187-C-A

61256996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9234384-G-A

61257342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9234747-G-A

61257620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9235032-G-A

61257677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9235076-T-C

61257845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9235250-A-G

61257890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9235294-T-A

61258198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9235579-G-A

61258654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9236010-T-A

61258654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9236010-T-C

61258918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9236256-T-A

61258959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9236301-T-C

61258991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9236332-A-G

61259338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9236817-C-T

61259592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9237127-A-G

61259607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9237142-T-C

61259752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9237278-C-T

61259794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9237320-G-A

61259794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9237320-G-T

http://identifiers.org/hco/8/GRCh38#61259856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9237381-A-C

61259882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, undefined
orthologous variants: 9237406-C-T

http://identifiers.org/hco/8/GRCh38#61260031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9237535-C-A

61260031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9237535-C-T

61260100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9237600-G-A

61260235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9237702-A-T

61260694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9238102-C-G

61260694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9238102-C-T

61260702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9238110-T-C

61262569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9240539-G-A

61262727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9240702-C-T

61262861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9241322-C-T

61262948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9241398-G-A

61262955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9241405-G-T

61267668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246935-C-G

61267964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9247225-A-G

61274019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9247260-T-A

61274031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9247272-T-A

61274031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9247272-T-C

61274154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9247398-G-A

61274154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9247398-G-T

http://identifiers.org/hco/8/GRCh38#61274245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9247481-C-A

61274290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9247526-G-T

61274388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9247621-A-G

61274659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9247906-C-T

61274695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9247943-C-T

61274944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9248161-G-A

http://identifiers.org/hco/8/GRCh38#61274964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9248181-C-A

61275048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9248547-G-A

61275260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9248745-G-A

61275451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9248999-G-A

61275521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9249070-G-A

61275521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9249070-G-T

61275565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9249102-T-G

61275822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9249323-C-T

61275847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9249349-T-C

61276065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9250020-A-G

61276138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9250089-A-G

61276145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9250096-A-G

61276318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9250261-A-G

61276320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9250263-G-T

61276477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9250410-A-G

61276849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9250791-A-G

61276849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9250791-A-T

http://identifiers.org/hco/8/GRCh38#61276953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9250897-C-A

61278558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9254744-G-C

61279130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9255562-G-A

61279479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9255887-C-T

61279586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9255993-G-C

61279647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9256049-G-A

61279647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9256049-G-C

61280198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9256659-A-G

http://identifiers.org/hco/8/GRCh38#61280283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9256749-A-C

61280626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9257147-G-A

http://identifiers.org/hco/8/GRCh38#61280643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9257162-C-A

61280747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9257243-A-G

61281199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9258013-T-G

61281220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9258034-T-C

61282896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9262180-T-G

61283078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9262331-T-G

61283487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9262719-T-C

61283487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9262719-T-G

61283501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9262733-A-G

61283591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9262799-C-G

http://identifiers.org/hco/8/GRCh38#61283813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9262999-A-C

61283813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9262999-A-T

61287699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9269080-G-A

61287851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9269189-A-G

61287851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9269189-A-T

http://identifiers.org/hco/8/GRCh38#61288126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#9269459-C-A

61288126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 9269459-C-T

61288184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9269516-C-T

61288565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9269890-G-A

61288903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9270211-T-C

61289776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9271105-G-A

http://identifiers.org/hco/8/GRCh38#61289878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9271215-A-C

61290042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9271369-T-G

61290156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9271481-G-A

61290235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9271561-G-A

61290385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9271702-T-C

61290513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9271826-C-G

61290575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9271884-C-G

61290783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9272082-A-G

61291337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9272582-G-A

61291463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9272740-G-T

61291492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9272768-T-C

61291522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9272798-G-A

61291612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9272876-A-G

61291708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9273015-G-A

61291710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9273017-C-T

61291761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9273074-G-A

http://identifiers.org/hco/8/GRCh38#61291883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9273190-C-A

http://identifiers.org/hco/8/GRCh38#61292086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9273756-A-C

61292086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9273756-A-G

61292404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9274051-G-A

61292417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9274059-T-C

61292641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9274262-A-G

61292682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9274306-G-A

61292682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9274306-G-C

61292719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9274344-A-G

61292948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9274581-T-C

http://identifiers.org/hco/8/GRCh38#61293070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9274700-C-A

61293203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9274832-C-G

61293203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9274832-C-T

61293449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9275075-G-C

61293449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9275075-G-T

61293481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9275105-A-T

61294117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9276166-A-G

61294134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9276183-G-C

http://identifiers.org/hco/8/GRCh38#61294175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9276233-C-A

61294175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9276233-C-T

61294385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9276475-G-C

http://identifiers.org/hco/8/GRCh38#61294549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9276656-C-A

http://identifiers.org/hco/8/GRCh38#61294565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9276672-A-C

61294610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9276717-T-G

61294734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9276821-A-T

61294797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9276879-A-G

61294885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9276966-T-C

61295205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9277237-C-T

61295234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9277257-A-G

61295329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9277356-G-A

61295336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9277363-A-G

61295339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9277366-A-G

61295339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9277366-A-T

61295551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9277568-G-T

61295614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9277631-G-A

61295614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9277631-G-C

61295862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9277829-A-T

61296318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9278266-A-G

61296687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9278639-T-C

61296892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9279074-G-T

61297140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9279224-G-A

61297644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9279646-T-A

61297644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9279646-T-G

61297683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9279685-T-C

61297723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9279732-C-T

61297741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9279745-G-A

61297762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9279766-T-C

61297873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9279872-T-C

61297952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9279933-A-T

61298763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9280523-G-T

61298802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9280568-G-A

61298802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9280568-G-T

61299062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9280805-T-A

61299148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9280882-G-C

61299545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9281256-G-A

61299545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9281256-G-C

61299545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9281256-G-T

61299697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9281408-G-T

http://identifiers.org/hco/8/GRCh38#61299717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9281428-C-A

61299717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9281428-C-G

61299717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9281428-C-T

http://identifiers.org/hco/8/GRCh38#61299813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9281543-C-A

61299813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9281543-C-T

61299852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9281582-A-G

61300175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 9281905-C-T

61300457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9282164-A-G

http://identifiers.org/hco/8/GRCh38#61300460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9282167-A-C

61300460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9282167-A-G

61300478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9282185-A-G

http://identifiers.org/hco/8/GRCh38#61300490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9282197-C-A

61300490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9282197-C-T

http://identifiers.org/hco/8/GRCh38#61300515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9282222-C-A

61300546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9282252-A-G

61300560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9282266-G-C

61300560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9282266-G-T

61300565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9282271-A-T

61300573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9282279-T-C

61300573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9282279-T-G

61300581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9282285-T-G

61300641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9282337-G-C

61300641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9282337-G-T

61300647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9282343-T-A

http://identifiers.org/hco/8/GRCh38#61300661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9282356-A-C

61300661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9282356-A-G

61300705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9282397-C-T

61300830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9282490-A-T

61300847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9282507-A-G

http://identifiers.org/hco/8/GRCh38#61300865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9282523-C-A

61300865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9282523-C-T

http://identifiers.org/hco/8/GRCh38#61300916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9282564-C-A

http://identifiers.org/hco/8/GRCh38#61300930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9282585-C-A

61300930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9282585-C-G

61301725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9283370-C-T

61301911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9283514-T-G

61301931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9283534-C-T

61302326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9283890-G-C

61302504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9284071-T-G

61302534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9284094-A-G

61302606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9284161-A-T

61303119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9284268-T-G

http://identifiers.org/hco/8/GRCh38#61303155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9284301-C-A

61303237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9284400-A-T

61303250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9284413-A-G

61303363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9284529-T-C

61303369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9284535-G-A

61303434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9284571-T-C

61303459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9284596-A-G

61303459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9284596-A-T

http://identifiers.org/hco/8/GRCh38#61303658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9284799-C-A

61303689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9284828-T-C

61304025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9285141-T-C

61304108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9285217-G-A

http://identifiers.org/hco/8/GRCh38#61304120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9285226-A-C

61304185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9285290-G-A

61304194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9285299-G-A

http://identifiers.org/hco/8/GRCh38#61304273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9285368-C-A

61304273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9285368-C-T

61304455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9285507-A-G

61304500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9285550-A-G

http://identifiers.org/hco/8/GRCh38#61304544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9285598-A-C

61304556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9285610-A-G

61304624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9285674-A-T

61304639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9285689-C-G

61304639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9285689-C-T

http://identifiers.org/hco/8/GRCh38#61304809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9285850-A-C

61304990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9286018-G-A

61307081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9286410-A-G

61307108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9286437-G-T

61307227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9286552-G-A

61307438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9286786-G-A

61307438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9286786-G-T

61307500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9286849-G-T

61307501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9286850-T-C

61307570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9286931-T-C

61308146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9287242-A-G

61308146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9287242-A-T

61308177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9287276-C-T

61308230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9287329-A-G

61308241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9287340-A-T

61308264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9287363-A-G

61308344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9287438-C-T

61308401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9287496-T-A

61308407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9287502-G-A

61308407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9287502-G-C

61308417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9287512-A-T

61309625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9287653-G-T

61309681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9287710-C-T

61309723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9287752-C-T

61309899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9287929-G-C

61309903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9287933-T-C

61309911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9287941-G-C

http://identifiers.org/hco/8/GRCh38#61309929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9287959-C-A

61310113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9288131-T-C

61310193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9288222-A-G

61310368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9288403-C-T

61310396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9288431-G-A

http://identifiers.org/hco/8/GRCh38#61310497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9288524-C-A

61310518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9288545-G-A

61310518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9288545-G-T

61310540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9288567-G-A

61310540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9288567-G-T

61310554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9288576-G-A

61310606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9288626-A-G

61311195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9289645-G-A

61311238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9289688-C-G

61311295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9289730-T-C

61311360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9289788-T-C

61311530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9289925-A-G

61311562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9289957-A-T

61311747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9290100-T-C

61311974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9290893-A-G

61311976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9290895-G-A

61312033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9290951-T-C

http://identifiers.org/hco/8/GRCh38#61312333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9291214-C-A

61312505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9291391-T-C

61312557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9291434-A-G

61312622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9291500-C-T

61312933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9296583-T-G

61312982-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9296623-A-T

61313096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9296731-C-G

61313115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9296741-A-T

61313246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9296871-G-A

61313334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9296958-G-A

61313491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9297104-G-C

61313907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9297441-G-A

61313956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9297487-A-T

61314044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9297566-T-C

61314274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9297828-G-A

61314357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9297903-G-A

61314357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9297903-G-C

61314459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9298004-A-T

61314688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9298110-G-C

61314860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9298250-A-T

61314919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9298309-G-T

61315007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9298394-A-G

61315108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9298510-C-T

61315258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9298659-C-T

61315506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9298848-T-C

61315629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9298960-T-C

61315686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9299015-A-G

61315688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9299017-G-T

61315779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9299110-T-C

http://identifiers.org/hco/8/GRCh38#61316982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9299558-C-A

61316988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9299564-A-G

61317044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9299614-G-T

61317195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9299756-G-A

61317308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9299860-A-T

http://identifiers.org/hco/8/GRCh38#61317492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9300075-A-C

61317632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9300301-A-G

61317712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9300429-A-G

61317764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9300487-T-A

http://identifiers.org/hco/8/GRCh38#61317882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9300669-C-A

61318051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9300831-G-A

61318100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9300873-G-T

61318108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9300881-T-C

61318298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9301052-T-C

http://identifiers.org/hco/8/GRCh38#61318324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9301081-A-C

61318336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9301092-A-G

61318478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9301225-T-A

61318497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9301244-A-G

61318763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9301495-G-T

61321148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9301765-C-T

61321197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9301824-G-T

61321375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9301965-A-G

61321420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9302045-A-G

61321843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9302437-T-G

61322035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9302603-C-G

61322106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9302672-A-T

61322188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9302757-G-C

61322192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9302761-G-A

61322371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9302896-T-A

61322371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9302896-T-C

61322371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9302896-T-G

http://identifiers.org/hco/8/GRCh38#61322532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9303030-C-A

61322730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9303487-T-C

61322744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9303532-A-G

61322771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9303566-C-G

61322837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9303702-C-G

61324873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9304177-C-T

61325080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9304390-G-A

61325139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9304448-G-A

61325334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9304721-G-A

61325523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9304873-C-T

61325536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9304886-A-T

61325537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9304887-T-C

61325553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9304903-T-C

61325997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9305318-C-T

61326202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9305533-G-T

61326302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9305631-T-G

61326307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9305636-T-C

61326352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9305681-G-A

61326583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9306047-G-A

61326689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9306211-A-T

61326755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9306274-C-T

61326911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9306411-A-G

61326983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9306478-C-T

61328077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9307608-T-G

61328200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9307698-G-A

61328544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9307782-C-T

http://identifiers.org/hco/8/GRCh38#61328668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9307916-C-A

61332312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9310684-G-C

61332320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9310693-C-T

61332429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9310798-G-A

61332574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9310940-T-C

61332671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9311018-C-G

61332671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9311018-C-T

61334422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9312810-C-T

61334444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9312836-A-G

http://identifiers.org/hco/8/GRCh38#61334456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9312847-A-C

61334476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9312867-T-C

http://identifiers.org/hco/8/GRCh38#61334568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9312962-C-A

61334743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9313125-T-C

61335519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9313213-C-T

61335539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9313232-G-A

61335551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9313244-G-A

61335717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9313411-C-T

61335944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9313634-T-A

61335945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9313635-G-A

61336101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9313796-C-T

61336126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9313811-G-T

61336194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9313868-C-T

61336271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9313921-C-T

61336324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9313978-A-G

http://identifiers.org/hco/8/GRCh38#61336487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9314067-A-C

http://identifiers.org/hco/8/GRCh38#61336730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9314366-C-A

61336730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9314366-C-T

61336800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9314439-G-C

61336820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9314460-C-G

61336932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9314564-T-A

61336984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9314610-G-A

61337086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9314730-C-G

61337087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9314731-A-G

http://identifiers.org/hco/8/GRCh38#61337093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9314737-A-C

61337093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9314737-A-G

61337271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9314855-G-A

61337324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9314869-T-G

61337353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9314898-T-C

61337372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9314915-C-T

61337375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9314918-T-C

61337377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9314920-T-C

61337456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9314987-G-A

61337543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9315047-C-T

61337717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9315215-A-G

61337732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9315230-A-G

61337791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9315285-G-A

61337796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9315290-T-G

61338620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9315476-T-C

61338678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9315530-C-T

61338761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9315619-C-T

61339134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9315850-A-G

61339262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9315962-G-A

61339324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9316012-G-A

61340595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9317433-C-T

61340776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9317608-G-A

61341032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9317854-G-A

61341345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9318164-G-T

61341783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9318592-G-C

61341959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9318766-G-A

61341971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9318778-C-T

61342168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9318982-C-G

61342689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9319503-T-C

61342717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9319531-T-C

61343252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9320334-A-T

61343254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9320336-G-A

61343254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9320336-G-C

61343256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9320338-T-C

61343429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9320500-C-T

61343631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9320665-G-A

61343790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9320841-G-T

61343794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9320845-T-A

61343931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9320976-A-G

61343953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9320995-G-A

61344064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9321093-C-T

61344138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9321166-C-G

http://identifiers.org/hco/8/GRCh38#61344155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9321182-C-A

61344365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9321325-A-G

61344433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9321372-C-T

61344468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9321409-C-T

61344499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9321440-G-A

61344527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9321461-G-C

61344885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9321781-G-A

61345208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9322069-T-C

61345562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9322427-G-T

61345667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9322530-T-C

61345712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9322571-G-A

61345969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9322806-T-G

61346408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9323184-G-A

http://identifiers.org/hco/8/GRCh38#61349645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9323989-C-A

61349850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9324179-C-G

61349850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9324179-C-T

61350284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9324407-G-A

61350302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9324425-T-C

61350404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9324523-G-A

61350407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9324526-T-C

61350413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9324532-A-G

61350465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9324585-A-G

61350626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9324762-T-C

61350783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9324899-C-T

61350819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9324930-T-C

61350841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9324951-C-T

61354270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9329973-C-G

61354270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9329973-C-T

http://identifiers.org/hco/8/GRCh38#61354491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9330230-A-C

61354634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9330364-T-A

61354638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9330368-T-C

61354676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9330406-A-G

http://identifiers.org/hco/8/GRCh38#61354797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9330514-C-A

61354810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9330528-T-C

61354970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9330555-A-G

61358074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9331243-A-G

61358258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9331427-C-T

61358356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9331507-C-G

61358479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9331638-T-C

61358499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9331657-C-T

61358608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9331752-C-T

61360494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9332077-G-A

61360676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9332234-T-C

61360771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9332326-T-A

61361294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9332413-T-C

61361326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9332445-A-G

http://identifiers.org/hco/8/GRCh38#61361404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9332526-A-C

61361545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9332658-G-A

61361586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9332699-C-T

61361693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9332805-G-A

61361703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9332815-C-T

61361969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9333091-G-T

61362043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9333167-G-A

61362118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9333239-G-A

61362235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9333327-C-T

61362330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9333418-A-G

61362393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9333482-T-G

61362402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9333489-C-T

http://identifiers.org/hco/8/GRCh38#61362410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9333497-C-A

61362464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9333552-C-T

61362661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9333749-C-G

61362661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9333749-C-T

61362857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9334052-T-C

61362867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9334062-C-T

61362953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9334154-G-A

61362973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9334171-A-G

61363052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9334238-G-A

61363052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9334238-G-T

61363115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9334292-C-G

61363379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9334548-C-T

61363444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9334606-A-T

61363749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9334898-C-G

61363810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9334936-T-C

61363875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9335027-A-T

http://identifiers.org/hco/8/GRCh38#61363892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9335138-C-A

61363907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9335153-T-A

61363958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9335202-T-A

61364050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9335293-C-T

61364065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9335308-T-A

http://identifiers.org/hco/8/GRCh38#61364106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9335352-C-A

61364106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9335352-C-T

61364162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9335414-A-G

61364357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9335596-A-G

61364361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9335600-T-C

61364574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9335790-A-G

61364596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9335812-G-A

61364737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9335958-C-T

61365091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9336311-G-A

61365112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9336332-C-T

61365237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9336450-A-G

61365629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

61365711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

61365713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

61365731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

61365756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

61365841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

http://identifiers.org/hco/8/GRCh38#61365922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9336833-A-C

61365922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9336833-A-T

61366250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9337117-A-T

61366282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9337151-G-T

61366409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9337272-G-A

61366409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9337272-G-C

61366436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9337452-A-T

61366469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9337485-T-G

http://identifiers.org/hco/8/GRCh38#61366482-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9337498-A-C

61366486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9337502-T-C

61366597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9337620-G-C

http://identifiers.org/hco/8/GRCh38#61366612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9337655-A-C

61366719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9337767-C-T

61366753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9337800-G-T

61367339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9338925-C-G

61367403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9338976-T-A

61367407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9338980-T-C

61368061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9339857-A-G

61368095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9339883-T-C

61371600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9346704-C-G

61371626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9346731-G-A

61371772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9346993-G-A

61372285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9347448-C-T

61372430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9347582-T-C

61372565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9347711-A-G

61372574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9347720-T-C

61372607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9347746-G-T

61372762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9347893-A-G

http://identifiers.org/hco/8/GRCh38#61372792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9347923-A-C

61372962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9348095-G-C

61373094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9348221-A-G

61373169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9348300-G-A

61374842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349061-T-C

61374842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349061-T-G

61374984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349200-A-T

61375005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349213-T-C

http://identifiers.org/hco/8/GRCh38#61375119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9349330-C-A

61375130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349341-C-T

61375150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349354-C-T

61375616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349514-G-T

61375786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349676-G-A

http://identifiers.org/hco/8/GRCh38#61375843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9349730-C-A

61375843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349730-C-T

61375947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349832-G-T

http://identifiers.org/hco/8/GRCh38#61376014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9349899-C-A

61376043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349928-T-C

http://identifiers.org/hco/8/GRCh38#61376069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9350009-A-C

61376087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9350028-A-G

61376215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9350165-G-C

61376237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9350188-C-T

61376238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9350189-G-A

61376238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9350189-G-C

61376238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9350189-G-T

61376268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9350282-C-G

61376324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9350361-T-C

61376454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9350498-G-A

61376454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9350498-G-T

http://identifiers.org/hco/8/GRCh38#61376560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9350607-C-A

61376560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9350607-C-T

61376569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9350616-A-G

61376617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 9350659-A-G

61376668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 9350710-G-A

61376683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 9350725-T-C

61376813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9350846-T-C

http://identifiers.org/hco/8/GRCh38#61376821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9350854-C-A

61376821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9350854-C-G

61376821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9350854-C-T

61376870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9350907-G-T

61376872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9350909-G-A

61376872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9350909-G-T

61376885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9350922-T-C

61376904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9350943-G-C

61376904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9350943-G-T

61376912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9350951-T-C

http://identifiers.org/hco/8/GRCh38#61376936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9350981-A-C

61376936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9350981-A-T

61376966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9351012-A-G

61377035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9351081-A-G

61377038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9351084-A-G

61377044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9351090-G-A

http://identifiers.org/hco/8/GRCh38#61377046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9351092-C-A

61377060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9351102-G-A

61377060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9351102-G-C

61377060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9351102-G-T

61377117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9351155-G-A

61377117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9351155-G-T

61377153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9351188-A-G

61377247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9351282-A-G

61377297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9351327-G-A

61377347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9351378-T-G

61377399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9351442-G-A

61377420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9351463-T-A

61377461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9351492-T-C

61377521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9351555-G-T

61377804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9351773-C-G

http://identifiers.org/hco/8/GRCh38#61377889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9351852-C-A

61378009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9351946-G-A

61378046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9351981-C-G

61378138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9352052-C-T

61378299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9352195-G-T

61378401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9352288-T-C

61378453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9352339-G-T

61378517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9352396-G-A

61378517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9352396-G-T

61378522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9352401-G-A

61378522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9352401-G-T

http://identifiers.org/hco/8/GRCh38#61378525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#9352404-C-A

61378625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9352678-G-T

61378786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9352965-C-T

61378870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9353073-C-T

61378971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9353174-G-T

61379071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9353266-A-G

61379087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9353282-A-G

61379160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9353354-T-C

61379171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9353365-G-T

61379275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9353461-G-A

61379909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9354012-A-G

61380041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9354106-A-G

61380065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9354116-A-G

61380144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9354179-C-T

61380157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9354192-G-A

61380275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9354296-C-T

61380349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9354362-A-G

61380621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9354917-G-A

61380851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9355210-A-G

61381061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9355424-G-T

61381099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9355464-A-T

61381106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9355471-C-T

61382014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9356062-T-C

61382025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9356073-C-G

61382039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9356087-T-C

61382153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9356198-T-C

61382269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9356301-T-C

61382717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9356625-G-A

61382905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9356796-G-T

61383038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9356911-C-T

61383245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9357096-T-C

61383289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9357140-A-T

61383378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9357231-C-T

61383658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9357498-T-C

61383766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9357602-T-C

61383786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23139
most severe consequence: intron variant
orthologous variants: 9357622-G-T