1449376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8550413-C-T

1449380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8550409-A-G

1449382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8550407-T-C

1449429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8550357-G-C

1449432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8550354-C-G

1449515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8550276-T-G

http://identifiers.org/hco/10/GRCh38#1449521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8550270-C-A

1449521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8550270-C-T

1449599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8550187-A-G

1449888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8549895-A-G

1450007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8549772-G-A

1450182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8549643-C-T

1450317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8549501-G-A

1450317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8549501-G-C

1450317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8549501-G-T

1450422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8549386-C-G

1450422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8549386-C-T

1450423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8549385-C-T

1450601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8549225-T-C

1450699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8549107-T-C

1450741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8549065-C-G

1450741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8549065-C-T

1450823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8548981-G-C

1450906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8548908-T-C

1450970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8548870-G-T

1451000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8548840-G-C

1451435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8547213-T-G

1451591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8547081-G-A

1451722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8546963-A-G

1455057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8545082-C-T

1455130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8545009-G-A

http://identifiers.org/hco/10/GRCh38#1455275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8544860-A-C

1455406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8544730-G-A

1455494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8544640-A-T

1455579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8544547-T-G

1455598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8544528-C-T

1455637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8544490-G-A

http://identifiers.org/hco/10/GRCh38#1455802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8544328-C-A

1455802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8544328-C-T

1455915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8544210-A-T

1456217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8543723-G-A

1456222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8543718-C-T

1456237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8543703-G-A

1456330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8543618-C-T

1456350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8543598-T-C

1456363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8543586-C-T

1456557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8543366-G-C

1456557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8543366-G-T

1456704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8543219-C-T

1457267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8542945-G-C

1457330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8542907-C-T

1461585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8540225-G-A

1463470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8538510-C-T

http://identifiers.org/hco/10/GRCh38#1466364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8536591-C-A

1466365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8536590-A-G

1466445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8536509-A-G

1466949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8535705-C-T

http://identifiers.org/hco/10/GRCh38#1467014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8535659-C-A

http://identifiers.org/hco/10/GRCh38#1467123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8535561-C-A

1467123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8535561-C-T

1467202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8535479-T-A

1467258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8535424-A-G

1467604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8535043-A-G

1467604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8535043-A-T

1467861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8534728-C-T

1468156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8534420-A-T

1468327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8534266-C-T

1468350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8534240-G-C

1468385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8534205-A-G

1468409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8534180-G-A

1468952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8533340-G-A

1468952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8533340-G-T

1469023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8533274-A-G

1469082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8533214-C-T

1469231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8533124-T-G

1469324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8533056-G-A

1469485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8532897-A-G

1470006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8532344-G-A

1470008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8532342-G-A

1470054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8532297-G-A

1470054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8532297-G-C

1470191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8532204-T-A

1470355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8532066-A-G

1470876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8531652-C-T

1470931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8531644-T-C

1471154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8531576-A-G

1471320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8531408-C-T

1471428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8531336-T-C

1471494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8531274-G-A

http://identifiers.org/hco/10/GRCh38#1471504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8531264-C-A

1471547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8531251-T-C

1471551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8531247-T-C

1471560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8531221-T-G

1471913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8530863-C-T

1471965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8530828-T-C

1472002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8530786-T-A

http://identifiers.org/hco/10/GRCh38#1472073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8530737-A-C

http://identifiers.org/hco/10/GRCh38#1472087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8530721-C-A

1472087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8530721-C-T

1473688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: -C-T

1475577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8527568-G-T

1476394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8526746-C-T

1476894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8526225-T-C

1476913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8526206-T-A

1482970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8519081-T-C

1483003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8519053-T-C

1483044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8519010-G-A

1483772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8518154-T-C

1483790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8518136-G-T

1483967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8517965-A-G

1484368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8517517-G-A

http://identifiers.org/hco/10/GRCh38#1484796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8517168-A-C

1484962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8517032-G-A

1484962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8517032-G-T

1485025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8516972-T-C

1485077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8516925-G-A

1485292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8516750-A-G

1485375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8516682-C-T

1485457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8516609-G-A

1485457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8516609-G-T

1485485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8516586-T-C

1485517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8516552-C-T

1485693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8516408-A-G

1485703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8516398-T-C

1485706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8516395-G-A

1485711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8516389-T-C

1485715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8516385-G-A

1485720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8516380-C-T

1485857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8516231-A-G

1486017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8516073-G-C

1486038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8516052-A-G

1486038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8516052-A-T

1486427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8515716-A-G

1486702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8515385-G-A

1486865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8515050-G-C

1486876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8515039-T-A

1487123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8514841-G-A

1487152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8514816-G-A

1487200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8514779-G-A

1487310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8514664-T-G

http://identifiers.org/hco/10/GRCh38#1487366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8514620-C-A

http://identifiers.org/hco/10/GRCh38#1487414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8514538-C-A

1487427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8514388-T-C

1487446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8514369-G-A

1487446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8514369-G-T

1487717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8514033-A-T

1487857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8513899-C-T

1488046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8513719-C-T

1488089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8513676-G-T

http://identifiers.org/hco/10/GRCh38#1488200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8513579-C-A

1488500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8513285-C-T

1488680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8513110-C-T

1488802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8512496-G-C

1488849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8512449-G-T

1488896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8512405-T-A

1489728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8511633-T-C

http://identifiers.org/hco/10/GRCh38#1491400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8508579-C-A

1491400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8508579-C-G

1491400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8508579-C-T

1491689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8508238-C-T

1491716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8508211-C-T

1491748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8508179-C-T

1491781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8508145-A-G

1491788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8508138-T-G

1491830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8508074-C-T

1491891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8508011-C-T

1492085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8507820-A-G

1493084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8505264-A-G

1493255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8505118-C-T

1493422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8504956-C-T

http://identifiers.org/hco/10/GRCh38#1495595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8504823-A-C

1495595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8504823-A-G

1495595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8504823-A-T

1495613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8504805-G-C

http://identifiers.org/hco/10/GRCh38#1495916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8504553-C-A

1500448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8503793-C-G

1500448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8503793-C-T

1501259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8502715-A-G

1501278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8502700-T-A

1501278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8502700-T-C

1501278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8502700-T-G

1501345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8502646-A-G

1501910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8502092-G-A

1502099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8501879-G-C

1502099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8501879-G-T

1502201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8501775-C-T

1502254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8501718-C-T

1502368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8501583-A-G

1502375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8501576-C-T

1502376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8501575-G-A

http://identifiers.org/hco/10/GRCh38#1502670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8500988-C-A

1502670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8500988-C-T

1502915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8500768-G-A

1502915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8500768-G-C

1504075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8499656-A-T

1504385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8499276-T-C

1504704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8498962-G-A

1504791-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8498843-A-T

1505414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8498552-T-C

1505448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8498518-G-T

1505882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8498220-T-A

1505882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8498220-T-C

1506103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8498085-T-C

1506114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8498074-T-C

1506180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8498003-T-G

1506267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8497933-C-T

http://identifiers.org/hco/10/GRCh38#1509114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8495153-A-C

1509125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8495142-T-C

1509199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8495067-A-G

1509351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8494915-T-C

1509598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8494666-C-T

1509626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8494638-C-G

1510637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8492917-T-C

1510637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8492917-T-G

1514688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8489067-G-A

1514842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8488915-C-G

1514885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8488873-A-G

1514887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8488866-G-A

http://identifiers.org/hco/10/GRCh38#1515012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8488735-C-A

1515012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8488735-C-G

1515012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8488735-C-T

1515870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8487713-T-C

1516633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8486991-A-G

1516891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8486746-A-G

1517041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8486595-C-T

1517057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8486578-C-G

1517091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8486544-T-C

1517098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8486537-T-G

1517131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8486504-G-A

http://identifiers.org/hco/10/GRCh38#1517144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8486491-A-C

1517157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8486478-C-T

http://identifiers.org/hco/10/GRCh38#1517279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8485981-C-A

1517444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8485833-G-A

1517444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8485833-G-C

http://identifiers.org/hco/10/GRCh38#1517577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8485704-C-A

1517703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8484032-C-T

1517886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8483864-G-C

http://identifiers.org/hco/10/GRCh38#1517919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8483829-C-A

1517919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8483829-C-T

1518011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8483730-C-T

1518159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8483598-G-A

1520966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: -C-T

1520967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: -A-G

1522826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8480120-G-A

1522829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8480117-C-T

1522870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8480072-C-T

1523128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8479735-G-A

1523291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8479583-A-T

1523556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8479359-C-G

1523556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8479359-C-T

http://identifiers.org/hco/10/GRCh38#1523572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8479343-A-C

1523689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8479229-A-G

1523706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8479212-A-T

1523738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8479181-A-G

1523915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8479013-C-T

1524207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8478770-A-G

1524297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8478672-A-G

1524491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8478446-A-G

http://identifiers.org/hco/10/GRCh38#1524656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8478284-C-A

1524691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8478250-C-T

1524709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8478224-G-A

1524721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8478189-C-T

1524743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8478148-G-A

1524743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8478148-G-C

1524805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8478085-G-A

1525021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8477627-C-G

1525071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8477583-G-A

1525131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8477524-T-A

1525135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8477520-T-C

1525139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8477516-C-G

1525358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8477307-C-T

http://identifiers.org/hco/10/GRCh38#1526931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8476582-C-A

1526932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8476581-T-C

1526932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8476581-T-G

1526965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8476551-G-T

1526967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8476549-G-A

1526967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8476549-G-C

1526967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8476549-G-T

1526975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8476541-C-T

1527003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8476508-A-G

1527005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8476506-G-T

1527041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8476470-G-T

1527048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8476463-T-A

1527048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8476463-T-C

1527052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8476459-A-G

1527149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8476391-A-G

1527245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8476296-T-C

1527363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8474975-G-A

http://identifiers.org/hco/10/GRCh38#1527440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8474902-A-C

1527884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8474504-A-G

1528302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8474080-C-T

http://identifiers.org/hco/10/GRCh38#1528381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8474053-A-C

1528596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8472848-C-T

1528657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8472784-G-A

1528657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8472784-G-C

1528704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8472737-C-T

1531306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8471013-C-T

1531460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8470879-T-A

1531460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8470879-T-C

1532760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8460979-G-T

1532821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8460913-G-T

1532968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8460759-G-T

http://identifiers.org/hco/10/GRCh38#1533090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8460636-C-A

1533922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8460150-G-C

1535055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8456371-G-A

http://identifiers.org/hco/10/GRCh38#1535065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8456361-C-A

1535093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8456335-A-G

http://identifiers.org/hco/10/GRCh38#1535105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8456319-C-A

1535105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8456319-C-T

http://identifiers.org/hco/10/GRCh38#1535121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8456303-C-A

1535121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8456303-C-T

1535124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8456300-A-G

http://identifiers.org/hco/10/GRCh38#1535675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8455744-C-A

1535739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8455678-C-T

1535756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8455661-G-A

1535793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8455621-A-G

http://identifiers.org/hco/10/GRCh38#1535802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8455611-C-A

1535802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8455611-C-T

1535909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8455503-C-T

1535958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8455454-A-G

http://identifiers.org/hco/10/GRCh38#1536095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8455370-C-A

1536136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8455332-T-C

1536172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8455292-G-T

1536282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8455171-C-T

http://identifiers.org/hco/10/GRCh38#1536311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8455141-A-C

1536311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8455141-A-G

1539619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8452967-G-C

1539840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8452746-C-T

1539978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8452612-G-T

1540088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8452503-A-G

http://identifiers.org/hco/10/GRCh38#1540155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8452432-A-C

1540338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8452244-T-C

1540360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8452223-C-G

1540396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8452187-T-A

1540396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8452187-T-G

1543028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8452102-C-T

1543086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8452040-T-G

1543197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8451916-C-T

1543542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8451560-C-T

1543588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8451513-G-A

1543891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8451204-G-A

1544213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

http://identifiers.org/hco/10/GRCh38#1544242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

1544249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

1544566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

1544617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

1544780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

1544794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

1546703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8447567-G-A

1550073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8443543-C-T

http://identifiers.org/hco/10/GRCh38#1550160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8443457-C-A

1550231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8443360-T-A

1550348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8443242-T-C

1550422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8443169-A-G

1550479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8443112-T-G

1550612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8442973-C-T

1552906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8439277-C-T

1553682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8438501-C-T

1553912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8438255-C-G

http://identifiers.org/hco/10/GRCh38#1553913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8438254-C-A

1553913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8438254-C-T

1558976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8435205-A-G

1558985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8435196-T-G

1559008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8435169-T-G

1559357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8434873-G-A

1559486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8434775-A-T

1559501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8434762-C-G

1559595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8434659-G-C

1559684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8434562-C-T

1559687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8434559-G-A

1559687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8434559-G-T

1559927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8434327-G-T

http://identifiers.org/hco/10/GRCh38#1559983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8434263-C-A

1560073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8434181-G-A

http://identifiers.org/hco/10/GRCh38#1560347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8433948-C-A

1560347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8433948-C-T

1560393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8433902-C-T

1566333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8431153-T-C

1566358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8431128-C-G

1566401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8431083-G-A

1566544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8430901-A-G

1566550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8430895-C-T

http://identifiers.org/hco/10/GRCh38#1566639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8430782-C-A

1566639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8430782-C-G

1566823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8430544-G-A

1566853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8430515-T-G

1568776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8428319-G-A

1569257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8428180-A-G

1569264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8428173-G-A

1569264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8428173-G-C

1569281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8428156-A-G

1569455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8428064-C-T

1569560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8427950-C-T

1569610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8427900-C-T

1569800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8427432-A-G

1569818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8427414-T-C

1570042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8427201-A-G

1570057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8427186-G-T

1570124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8427094-T-A

1570204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8427013-T-A

1570345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8426879-T-C

1570360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8426864-C-T

1571388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8422394-G-A

1571417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8422365-A-T

1571502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8422282-A-G

1571573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8422216-A-G

1573081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8421557-G-T

1573124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8421537-A-G

1574795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8420779-C-G

1575334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8420257-G-C

1575499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8420082-G-A

1575610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8419937-G-A

1578765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8416571-C-G

1578765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8416571-C-T

1578864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8416485-A-T

1578956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8416421-G-A

1579017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8416341-T-G

1579028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8416325-C-T

1579179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8416148-G-C

1579302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8416016-C-T

1579435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8415881-G-A

1579489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8415826-A-G

1579490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8415825-G-T

1579520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8415800-C-T

1579716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8415588-C-T

1581079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8414701-C-T

1581094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8414686-C-T

1581095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8414685-T-G

1581119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8414666-C-T

1581143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8414644-C-T

1581587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8414231-G-C

1581838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8414022-G-A

1581838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8414022-G-C

1581857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8414003-T-C

1581869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8413991-T-C

1581901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8413941-A-G

1581901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8413941-A-T

1582287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8413586-G-A

http://identifiers.org/hco/10/GRCh38#1582388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8413521-C-A

1582388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8413521-C-T

1583048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8410578-C-G

1583048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8410578-C-T

1583338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8410271-A-G

1583609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8410001-C-T

1583765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8409866-A-G

1583933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8409674-C-T

http://identifiers.org/hco/10/GRCh38#1586582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8406874-C-A

1586969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8406482-A-G

http://identifiers.org/hco/10/GRCh38#1587042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8406419-A-C

1587352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8406115-G-C

1587397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8406069-C-T

1590494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8400597-C-T

1590502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8400589-G-T

1590535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8400556-A-G

1590590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8400501-G-A

http://identifiers.org/hco/10/GRCh38#1591697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8398830-C-A

1591697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8398830-C-G

http://identifiers.org/hco/10/GRCh38#1591702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8398816-C-A

1591725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8398798-G-A

1591743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8398780-A-G

1591767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8398756-T-C

1591960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8398559-C-G

1591972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8398547-G-A

1592261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8398259-G-A

1592261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8398259-G-T

1593399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8398210-T-A

1593399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8398210-T-C

1593452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8398155-G-A

1593541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8398103-A-T

1594447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8397498-C-T

1594507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8397437-G-A

1594507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8397437-G-C

1594598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8397323-C-T

1594754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8397167-G-T

1594829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8397082-C-T

1594942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8396981-G-A

1594942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8396981-G-T

1594983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8396946-A-G

1595025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8396892-T-C

1595045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8396872-C-T

1595604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8396070-C-T

1595619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8396054-C-G

1595619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8396054-C-T

1595680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8396011-A-G

http://identifiers.org/hco/10/GRCh38#1595837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8395884-C-A

1596131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8395604-G-T

1596155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8395580-T-C

1596377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8395363-C-T

1596387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8395353-C-G

1596387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8395353-C-T

1596530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8395210-A-G

1596661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8395031-G-A

1596661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8395031-G-C

1596699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8394995-G-A

1596768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8394938-G-T

1596830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8394876-A-G

1599009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8393548-A-G

1599321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8393256-A-T

http://identifiers.org/hco/10/GRCh38#1599370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8393207-C-A

1599412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8393166-C-G

1599412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8393166-C-T

1599462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8393117-G-A

1599608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8392968-C-T

1599646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8392922-C-T

1600263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8392037-A-T

1601105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8391502-C-T

1601141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8391478-C-T

1601146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8391473-T-C

1601350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8391237-G-C

1601569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8391052-T-G

1601935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8390718-A-G

1601996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8390663-G-A

1602007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8390652-G-C

1602039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8390621-G-A

1602253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8390031-G-A

1602259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8390025-G-A

1602442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8389844-G-A

1602515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8389759-G-A

http://identifiers.org/hco/10/GRCh38#1602565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8389705-A-C

1603436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8389374-T-A

1603436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8389374-T-G

1603560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8389249-G-A

1604803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8387575-T-G

1604886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8387496-G-C

1604886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8387496-G-T

1605026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8387316-G-A

1605144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8387192-C-G

1605411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8386916-C-T

1605417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8386910-T-C

1606871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8385783-A-G

1606972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8385682-T-C

1607584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8385143-C-T

1607633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8385092-G-A

1608079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8384619-C-T

1608102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8384595-T-A

1608147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8384554-T-A

1609514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8383563-A-G

1609634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8383473-A-G

1609683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8383395-T-G

1609714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8383365-C-T

1609802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8383273-G-T

1609891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8383184-G-C

1609896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8383179-G-A

1609896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8383179-G-C

1610468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8382107-G-A

1610607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8381931-G-A

http://identifiers.org/hco/10/GRCh38#1610612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8381926-A-C

1610729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8381703-T-A

1610773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8381679-C-T

1610775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8381677-C-T

1610792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8381660-A-G

1610871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8381575-T-C

1610895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8381553-T-A

http://identifiers.org/hco/10/GRCh38#1611025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8381423-C-A

1611025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8381423-C-T

http://identifiers.org/hco/10/GRCh38#1611771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8380131-A-C

1611774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8380128-G-A

1611865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8380029-G-A

1611874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8380020-T-C

1613030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8378376-C-T

1613326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8378112-A-G

1613343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8378008-C-T

1613461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8377873-G-A

1613568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8377762-G-A

1613704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8377625-A-G

http://identifiers.org/hco/10/GRCh38#1613886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8377442-C-A

1614008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8377317-G-A

1614109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8377201-C-T

http://identifiers.org/hco/10/GRCh38#1614112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8377198-A-C

1614119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8377191-T-C

1615174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8376042-G-C

1615737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8375424-G-A

1615793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8375354-G-A

1615813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8375334-C-T

1615854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8375292-G-A

1615854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8375292-G-T

http://identifiers.org/hco/10/GRCh38#1616031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8375130-C-A

1616031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8375130-C-G

1616059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8375102-G-A

1616063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8375097-G-T

1616107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8375051-G-A

1616196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8374973-T-C

1616210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8374959-G-C

1616218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8374951-G-A

1616218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8374951-G-T

1618328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8374133-G-C

1619081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8373086-A-G

1619098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8373061-G-C

http://identifiers.org/hco/10/GRCh38#1619255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8372908-C-A

1625254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8370504-C-T

1627184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8368927-G-A

1627250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8368865-G-A

1627275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8368839-C-T

1627489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8368391-A-G

1627653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8368217-G-T

1627819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8368071-C-T

1628013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8366904-G-A

1628013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8366904-G-T

1630173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8364190-T-G

1630209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8364154-G-A

1630256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8364122-G-A

http://identifiers.org/hco/10/GRCh38#1631248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8362461-C-A

1631248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8362461-C-T

1631275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8362439-G-T

1631310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8362405-C-T

1631590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8362044-C-T

1631776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8361863-T-A

1631821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8361817-T-C

1631847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8361792-A-G

1632015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8361679-C-G

http://identifiers.org/hco/10/GRCh38#1632097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8361595-A-C

1632191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8361512-A-G

http://identifiers.org/hco/10/GRCh38#1634503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8361197-C-A

1634503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8361197-C-T

1634868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8360837-G-A

1635107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8359846-G-A

1635282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8359669-T-C

1635556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8359415-T-C

1635794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8358763-A-G

1635882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8358681-G-T

1635996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8358582-G-A

1635997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8358581-T-C

1636001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8358577-G-A

1636025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8358552-T-A

1636155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8358418-G-A

1637759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8356548-G-A

1637759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8356548-G-T

1637781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8356528-G-A

http://identifiers.org/hco/10/GRCh38#1637836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8356471-C-A

1637836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8356471-C-T

1638480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8355837-T-C

1638642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8355733-G-A

1638832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8355559-C-T

1638856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8355535-T-A

1638934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8355460-G-T

1638962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8355434-A-G

1639009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8355383-G-A

1639136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8355267-G-A

1639136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8355267-G-T

http://identifiers.org/hco/10/GRCh38#1639175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8355231-C-A

1639175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8355231-C-G

1640229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8354581-T-A

1640229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8354581-T-C

1640348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8354469-C-T

1640503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8354313-T-C

http://identifiers.org/hco/10/GRCh38#1640699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8354074-C-A

1640953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8353834-A-G

1640979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8353807-G-A

1640979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8353807-G-T

1641108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8353674-A-G

1641150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8353627-C-T

1643312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8351048-C-T

1643313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8351047-A-G

1643361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, undefined
orthologous variants: 8350999-C-T

1643590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, undefined
orthologous variants: 8344589-T-C

1643721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, undefined
orthologous variants: 8344443-C-T

1643927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8344219-A-G

1644185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8343968-G-T

1644232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8343921-C-T

http://identifiers.org/hco/10/GRCh38#1644440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8343714-A-C

1644507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8343589-A-T

1644664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8343429-C-T

1644665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8343428-A-G

1644735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8343361-A-T

1646278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8338274-G-T

1646424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8338148-T-C

1646427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8338145-C-T

1646522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8338048-G-A

1646646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8337889-A-G

1646719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8337839-C-T

1647041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8337522-C-T

1647059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8337510-C-T

1647108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8337465-C-G

1647108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8337465-C-T

1647130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8337443-C-T

1647253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8337317-G-C

1647973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8336940-C-T

1648312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8336591-G-A

http://identifiers.org/hco/10/GRCh38#1648402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8336479-C-A

1648727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8335966-C-G

1648733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8335960-A-G

1648841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8335854-G-A

1648841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8335854-G-T

1648854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8335840-C-G

1650141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8334524-G-A

1650325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8334345-G-A

1650512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8333983-G-A

1650532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8333945-G-A

http://identifiers.org/hco/10/GRCh38#1650881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8333586-C-A

1650881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8333586-C-T

1650883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8333584-C-T

1650994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8333489-A-G

1651059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8333423-C-T

1651175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8333305-C-T

1651195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8333285-G-A

1651692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8332774-A-G

1651710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8332757-C-T

1651879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8332585-C-T

1655681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8330199-A-G

1655966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8329819-G-C

http://identifiers.org/hco/10/GRCh38#1655978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8329813-C-A

http://identifiers.org/hco/10/GRCh38#1656078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8329745-C-A

http://identifiers.org/hco/10/GRCh38#1656215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8329607-C-A

1656348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8329460-G-A

1657694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8329004-G-A

1657733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8328961-T-C

1657733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8328961-T-G

1657762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8328931-G-A

1657762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8328931-G-C

1657805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8328896-C-T

1658685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8328367-T-A

http://identifiers.org/hco/10/GRCh38#1659408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8327574-C-A

1659436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8327542-A-G

1659496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8327489-T-C

1660333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8326988-T-C

1660446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8326888-C-T

1660491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8326842-T-C

1660549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8326801-G-T

http://identifiers.org/hco/10/GRCh38#1660584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8326765-C-A

1660712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8326624-C-G

1661301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8326506-T-G

1664848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8323016-G-A

1664924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8322962-G-C

1665474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8322431-C-T

1665540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8322353-G-A

1665686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8322204-G-A

1665728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8322157-G-A

1665943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8321943-C-T

1666850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8320219-C-G

1666891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8320179-A-T

1667426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8317260-A-G

1667609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8317066-C-T

1668261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8316377-T-C

1670576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8315667-C-T

1670796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8315439-C-T

1670852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8315384-G-A

1670958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8315274-C-T

1671202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8315028-A-G

http://identifiers.org/hco/10/GRCh38#1671234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8314986-C-A

1671234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8314986-C-T

1671618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8314598-C-T

1672826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8313117-G-A

1673003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8312914-C-G

1673187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8312744-C-G

1673211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8312720-T-C

1673267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8312672-T-G

1673285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8312657-C-T

http://identifiers.org/hco/10/GRCh38#1673390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8312558-A-C

1673393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8312555-G-A

1673604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8311650-A-G

1673700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8311562-G-A

1673761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8311503-C-T

1673848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8311393-G-A

1673865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8311372-C-G

1673865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8311372-C-T

1673883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8311349-T-A

http://identifiers.org/hco/10/GRCh38#1673893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8311339-C-A

1673893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8311339-C-G

1674000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8310720-A-T

1674036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8310685-G-T

1674065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8310656-A-G

1674072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8310655-G-C

http://identifiers.org/hco/10/GRCh38#1674091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8310639-A-C

1674171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8310556-T-C

http://identifiers.org/hco/10/GRCh38#1674240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8310487-C-A

1674272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8310455-C-T

1674307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8310420-T-C

1674347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8310380-G-A

1674372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8310355-C-T

1674426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8310319-T-C

1674491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8310263-A-G

1674505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8310248-A-G

1674559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8310195-C-T

1674739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8310008-G-A

http://identifiers.org/hco/10/GRCh38#1674740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8310007-A-C

1674777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8309964-A-G

1674779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8309962-A-T

1674807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8309931-G-A

1675883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8309312-A-T

1675896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8309299-A-T

1675917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8309278-G-A

1675917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8309278-G-T

1675941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8309250-C-G

1675945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8309246-C-T

1676046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8309133-C-T

1676144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8309049-G-A

1676144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8309049-G-T

1676164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8309029-A-G

1676180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8309013-G-A

http://identifiers.org/hco/10/GRCh38#1676993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8308329-C-A

1677259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8308131-T-G

1677396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8307991-G-A

http://identifiers.org/hco/10/GRCh38#1677518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8307865-C-A

1677727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8307618-G-A

1677790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8307576-G-A

1677836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8307530-T-C

1677997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8307313-T-C

1678065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8307242-A-T

1678145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8307162-G-A

1678145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8307162-G-T

1678202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8307094-G-C

1678706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8306191-C-G

1678756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8306135-T-C

1678767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8306124-C-T

1678823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8306071-C-G

1679090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8305761-C-T

1679262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8305565-T-C

1679364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8305467-C-T

1681066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8304591-G-A

1681212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8304442-T-C

1681312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8304343-A-G

1681636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8304020-T-G

1681643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8304013-T-C

http://identifiers.org/hco/10/GRCh38#1681773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8303882-A-C

1681879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8303784-G-A

1681879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8303784-G-T

1681899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8303768-G-A

1681909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8303757-A-G

1682224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8303014-G-A

1682224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8303014-G-C

1682535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8302670-C-T

1682960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8302347-C-T

1682977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8302331-G-A

1682977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8302331-G-T

1683044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8302276-C-T

1683069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8302254-A-G

1683088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8302235-A-G

1683146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8302188-T-C

http://identifiers.org/hco/10/GRCh38#1683199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8302133-A-C

1683541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8301789-G-C

1683541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8301789-G-T

1683554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8301776-C-T

1683741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8301600-A-G

http://identifiers.org/hco/10/GRCh38#1684081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8301243-C-A

1684081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8301243-C-T

1684206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8301122-A-G

1684245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8301082-T-C

1684353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8300977-G-A

http://identifiers.org/hco/10/GRCh38#1684400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8300936-C-A

1684780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8300526-T-C

1684906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8300408-G-A

1685661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8299986-A-G

http://identifiers.org/hco/10/GRCh38#1686179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8298607-A-C

1686554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8298239-G-A

1686585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8298212-G-A

http://identifiers.org/hco/10/GRCh38#1686600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8298197-C-A

1686785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8298012-T-C

1686832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8297966-C-T

1687529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8297521-C-T

1687534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8297516-A-T

1687640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8297404-A-T

1687710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8297342-C-T

http://identifiers.org/hco/10/GRCh38#1687728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8297320-C-A

1687732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8297316-T-C

1687738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8297310-G-A

1687745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8297291-G-T

1687773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8297263-G-A

1687841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8297180-A-G

1688172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8296823-G-A

1688172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8296823-G-C

1688175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8296820-C-G

1688320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8296682-G-A

1688320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8296682-G-C

1688331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8296669-T-G

1688430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8296566-G-A

1689468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8295761-A-T

1689488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8295745-G-A

1689659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8295560-A-T

1689677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8295536-G-A

1689677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8295536-G-C

1689814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8295400-A-T

http://identifiers.org/hco/10/GRCh38#1689861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8295359-C-A

1689861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8295359-C-T

1690224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8295033-C-T

1690290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8294969-A-G

1693036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8292880-C-G

http://identifiers.org/hco/10/GRCh38#1693147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8292777-C-A

1693186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8292738-G-A

1693349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8292063-G-A

1693361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8292055-T-A

1693845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8291749-T-C

1694350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8291280-G-A

1694350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8291280-G-T

1694368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8291262-G-A

1694418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8291216-C-T

1694554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8291075-G-T

1694735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8290928-C-T

1694853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8290820-G-T

1694901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8290771-G-A

1694901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8290771-G-T

1695036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8290655-T-C

http://identifiers.org/hco/10/GRCh38#1695050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8290641-C-A

1695073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8290617-T-G

http://identifiers.org/hco/10/GRCh38#1695104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8290574-A-C

1695134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8290543-C-G

1695134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8290543-C-T

1695256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8290425-T-A

1695353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8290347-T-C

1695412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8290287-C-T

1695469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8290225-G-T

1695471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8290223-C-T

1695575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8290127-G-C

1695721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8290013-T-C

1695748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8289986-A-G

1695791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8289940-T-A

1695791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8289940-T-G

1696586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8289529-T-C

1697644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8288131-A-G

1697648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8288127-G-A

1697847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8287920-C-G

1697847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8287920-C-T

http://identifiers.org/hco/10/GRCh38#1697872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8287894-A-C

1697905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8287856-T-C

1697966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8287798-T-A

1697967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8287797-A-T

1697975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8287788-C-T

1698440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8286314-G-T

http://identifiers.org/hco/10/GRCh38#1705913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8286005-C-A

http://identifiers.org/hco/10/GRCh38#1706152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8285763-C-A

1706335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8285579-A-G

1707191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8281057-G-A

1707218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8281029-T-C

1707422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8280819-G-A

1707582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8280656-G-C

1707638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8280599-G-A

1707638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8280599-G-C

1707667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8280590-T-C

http://identifiers.org/hco/10/GRCh38#1707682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8280570-C-A

1707885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8280355-G-T

1708139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8280106-T-C

1708483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8279777-A-T

1708501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8279759-T-A

1708505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8279755-T-A

1708505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8279755-T-C

1709030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8279142-G-A

1709107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8279047-C-T

1709529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8278638-C-T

1709543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8278593-A-T

1709545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8278591-A-T

1709767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8278349-C-T

1710188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8277926-C-T

1710294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8277819-T-C

1710315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8277798-G-A

1710724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8277489-C-T

1710765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8277447-G-A

1711173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8277271-G-A

1711178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8277266-C-T

1711377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8277134-C-T

1711446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8277062-G-A

1711670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8276858-T-C

1711711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8276827-G-A

http://identifiers.org/hco/10/GRCh38#1711739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8276795-A-C

1712132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8275917-C-T

1712219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8275845-G-C

1712268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8275797-T-A

1712419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8275689-A-T

1712445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8275659-G-T

1712539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8275581-C-T

1712928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8275502-C-T

1712941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8275489-T-G

1712962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8275468-A-T

1715383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8274489-A-T

1715420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8274456-G-A

1716634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8273121-A-G

1716873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8272886-C-G

1716873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8272886-C-T

1718080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8271970-G-A

1718083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8271930-G-A

1718105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8271906-C-T

1718185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8271811-G-A

1718185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8271811-G-T

1718430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8271600-G-A

http://identifiers.org/hco/10/GRCh38#1718500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8271542-C-A

1718528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8271514-C-T

1718562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8271479-C-T

1718617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8271424-T-C

1720850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8268719-T-A

1720894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8268691-T-C

1720967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8268629-G-A

1720968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8268628-C-T

1721007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8268579-G-A

1721059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8268528-A-G

1721059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8268528-A-T

1721436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8268261-C-T

1721449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8268248-T-C

1721958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8267850-G-T

1722064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8267777-T-C

1722795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8266977-G-A

1722795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8266977-G-T

1722822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8266950-A-G

1722858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8266914-G-C

1722881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8266882-G-T

1723021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8266816-T-A

1723039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8266801-C-G

1723163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8266698-C-G

1723290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8266579-A-G

1723303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8266544-T-C

1723366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8266482-A-G

1723367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8266481-G-A

1723623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8265966-G-A

1723623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8265966-G-C

1723623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8265966-G-T

1723673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8265924-C-G

1723712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8265885-C-T

1723755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8265837-T-A

1723874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8265703-A-G

1723969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8265619-C-T

http://identifiers.org/hco/10/GRCh38#1725557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8265123-A-C

1725713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8265016-T-C

1725783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8264949-G-T

1725895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8264838-G-A

1726035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8264701-C-T

1726090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8264648-G-T

1726128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8264614-C-T

http://identifiers.org/hco/10/GRCh38#1726198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8264556-C-A

1726198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8264556-C-T

http://identifiers.org/hco/10/GRCh38#1726560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8264386-A-C

1726560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8264386-A-G

1726592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8264354-C-T

1726614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8264314-A-T

http://identifiers.org/hco/10/GRCh38#1726660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8264273-A-C

1726672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8264261-C-T

1726685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8264248-C-T

1726835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8264118-G-A

1727294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8263482-C-T

1727401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8263379-G-A

1727438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8263342-C-T

1727453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8263238-C-G

1727555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8262920-G-A

1727676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8262768-C-T

1727807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8262609-T-A

1727939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8262495-A-G

1728248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8262168-G-C

1728666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8261749-T-A

1728731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8261680-A-G

1728948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8261485-A-G

1729048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8261388-C-T

1729049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8261387-T-G

1729059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8261369-A-G

1729659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8260791-C-T

1729660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8260790-G-A

1729660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8260790-G-T

1729668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8260782-T-A

1729929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8260553-A-G

1729958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8260524-G-A

1730139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8260125-T-A

1730240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8260041-G-A

1730292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8259988-G-A

1730292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8259988-G-C

1730292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8259988-G-T

1730321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8259979-C-G

1730373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8259929-G-A

1730373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8259929-G-T

1730404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8259904-C-T

1730472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8259847-G-A

http://identifiers.org/hco/10/GRCh38#1730562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8259747-A-C

1730964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8259363-C-T

1731107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8259228-G-A

1731305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8259040-A-T

1731328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8259017-A-G

1731390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8258955-A-G

http://identifiers.org/hco/10/GRCh38#1731475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8258870-C-A

1731482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8258861-G-C

1731522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8258812-T-C

1731585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8258749-G-C

1731755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8258588-C-T

1731789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8258513-G-A

1732135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8258184-A-G

1732354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8258005-G-A

1732354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8258005-G-C

1732354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8258005-G-T

http://identifiers.org/hco/10/GRCh38#1732396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8257963-C-A

1732919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, undefined
orthologous variants: 8257446-C-T

1732921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron_variant, undefined
orthologous variants: 8257444-C-T

1733080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8257259-G-A

http://identifiers.org/hco/10/GRCh38#1733161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8257190-C-A

1733333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8257058-A-G

1733333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8257058-A-T

1733351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8257039-T-C

1733451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8256939-G-T

http://identifiers.org/hco/10/GRCh38#1733458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8256932-C-A

1733648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8256713-T-A

1733725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8256639-A-G

1733781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8256580-T-C

1733915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8256449-A-T

1733921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8256442-T-C

1734141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8256224-C-T

http://identifiers.org/hco/10/GRCh38#1734259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8256137-C-A

1734285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8256112-G-T

http://identifiers.org/hco/10/GRCh38#1734351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8256047-C-A

1734351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8256047-C-T

1734548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8255856-C-T

1734751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8255659-T-C

1734923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8255513-C-T

1735360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8255085-T-A

http://identifiers.org/hco/10/GRCh38#1735439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8255010-C-A

1735779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8254663-A-G

1735800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8254642-G-T

1735817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8254625-G-A

1735932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8254534-A-G

1735991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8254469-C-G

1736007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8254458-T-C

1736025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8254440-G-T

1736041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8254427-T-G

1736059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8254414-A-G

1736101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8254361-A-G

1736132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8254332-C-T

1736431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8254021-T-C

1736438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8254014-C-T

1736454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8253998-A-G

1736620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8253834-C-T

1736834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8253596-C-T

1736919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8253502-G-A

1736919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8253502-G-T

http://identifiers.org/hco/10/GRCh38#1736971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8253456-C-A

1736971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8253456-C-G

1736971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: intron variant
orthologous variants: 8253456-C-T

http://identifiers.org/hco/10/GRCh38#1737224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#8253190-C-A

1737224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 8253190-C-T

1737260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: 5 prime UTR variant
orthologous variants: 8253151-G-A

1737260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: 5 prime UTR variant
orthologous variants: 8253151-G-C

1737260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: 5 prime UTR variant
orthologous variants: 8253151-G-T

http://identifiers.org/hco/10/GRCh38#1737288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8253122-A-C

1737288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: 5 prime UTR variant
orthologous variants: 8253122-A-G

1737288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: 5 prime UTR variant
orthologous variants: 8253122-A-T

http://identifiers.org/hco/10/GRCh38#1737320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8253101-A-C

1737320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: 5 prime UTR variant
orthologous variants: 8253101-A-G

1737358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 8253062-T-A

1737363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 8253057-T-G

1737391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: 5 prime UTR variant
orthologous variants: 8253027-T-C

1737416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 8252999-G-A

1737416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 8252999-G-T

1737426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: 5 prime UTR variant
orthologous variants: 8252989-G-C

http://identifiers.org/hco/10/GRCh38#1737466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8252958-C-A

1737466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 227
most severe consequence: 5 prime UTR variant
orthologous variants: 8252958-C-T