217427012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187084464-G-T

217427518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187083904-A-G

217427770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187083664-A-G

217427868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187083566-G-A

217427901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187083524-T-C

http://identifiers.org/hco/1/GRCh38#217427950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187083477-A-C

217427950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187083477-A-G

217428024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187083263-T-C

http://identifiers.org/hco/1/GRCh38#217428117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187083155-C-A

217428140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187083132-A-G

217428151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187083127-A-G

217428151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187083127-A-T

217428211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187083070-G-T

217428407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187082893-A-G

217428488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187082812-T-C

217428499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187082802-T-A

217428518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187082783-G-C

217428601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187082696-C-G

217428813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187082563-T-A

217428872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187082508-T-C

217428923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187082474-T-A

217429052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187082366-G-A

217429052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187082366-G-C

217429357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187082093-C-T

217429486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187081999-C-T

217429498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187081986-T-C

217429498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187081986-T-G

217429537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187081948-T-C

217430172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187081662-T-C

http://identifiers.org/hco/1/GRCh38#217430254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187081587-C-A

217430280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187081561-A-G

217430341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187081500-G-A

217430383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187081467-A-T

http://identifiers.org/hco/1/GRCh38#217430492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187081360-C-A

http://identifiers.org/hco/1/GRCh38#217430760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187081127-C-A

217430760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187081127-C-T

217430827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187081068-A-G

217430861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187081034-A-G

217430936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187080961-A-G

217431010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187080890-G-T

http://identifiers.org/hco/1/GRCh38#217431070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187080839-C-A

217431070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187080839-C-G

217431101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187080807-G-C

217431101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3 prime UTR variant
orthologous variants: 187080807-G-T

217431179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: missense variant
orthologous variants: 187080738-G-T

http://identifiers.org/hco/1/GRCh38#217431232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187080685-C-A

217431638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187080459-C-T

217431819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187080291-T-C

217433833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187079284-G-C

217434180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187078912-A-T

217434191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187078901-G-T

http://identifiers.org/hco/1/GRCh38#217434396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187078736-C-A

217434551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187078605-A-T

217434564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187078592-C-T

217434568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187078588-A-G

217434607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187078553-C-T

217434616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187078544-T-C

217434616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187078544-T-G

217434694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187078466-A-T

http://identifiers.org/hco/1/GRCh38#217435956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187077121-A-C

217436099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187076931-G-A

217445290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187076844-T-G

http://identifiers.org/hco/1/GRCh38#217445304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187076830-A-C

217445425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187076715-G-A

217445513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187076641-T-A

217445904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187076271-T-C

217445960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187076217-T-A

217446101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187076063-G-A

217446435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187075395-T-A

217446435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187075395-T-C

217446435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187075395-T-G

http://identifiers.org/hco/1/GRCh38#217446500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187075341-A-C

http://identifiers.org/hco/1/GRCh38#217446695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187075145-C-A

217446695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187075145-C-T

217446809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187075072-T-C

217446942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187075026-G-A

217447123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, missense_variant
orthologous variants: 187074875-T-C

217447195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187074827-T-C

217449147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187073854-G-A

217449147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187073854-G-T

217449158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187073844-A-G

217449219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187073798-T-C

217449275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: missense variant
orthologous variants: 187073744-G-C

217449275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: missense variant
orthologous variants: 187073744-G-T

217449391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187073623-A-G

217449956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187073063-T-C

217449971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187073048-G-A

http://identifiers.org/hco/1/GRCh38#217450166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187072869-C-A

217450166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187072869-C-T

217450203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187072832-C-T

217450251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187072781-C-T

217450401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187072673-T-C

http://identifiers.org/hco/1/GRCh38#217450488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187072589-C-A

217451111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187072060-G-A

217452458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187070163-C-T

217452593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187070047-C-T

217452804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187069880-G-A

217452891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187069817-T-A

217452891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187069817-T-C

217453161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187069553-C-T

217453165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187069549-T-C

217453250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187069473-C-T

http://identifiers.org/hco/1/GRCh38#217453725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187068967-C-A

217453850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187068840-T-C

217453850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187068840-T-G

217453893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187068798-G-A

217454081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187068584-G-C

217455070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187068037-G-A

217455136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187067969-G-A

217455136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187067969-G-C

217455143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187067962-G-A

http://identifiers.org/hco/1/GRCh38#217455171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187067935-A-C

217455189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187067920-T-C

217455198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187067911-T-C

217457774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187067772-T-A

217457791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187067755-T-C

217461070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187066669-T-C

217461075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187066668-C-T

217461190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187066590-T-A

217461190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187066590-T-G

217461209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187066577-T-C

217461247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187066544-C-T

217461315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187066488-C-T

217461400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187066392-C-T

http://identifiers.org/hco/1/GRCh38#217461574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187066226-C-A

217461632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187066180-T-G

217461652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187066161-T-C

http://identifiers.org/hco/1/GRCh38#217462467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187065296-A-C

217462467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187065296-A-G

217468896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187062135-T-C

217469010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187062029-T-C

217469124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187061916-T-C

http://identifiers.org/hco/1/GRCh38#217469125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187061915-A-C

http://identifiers.org/hco/1/GRCh38#217469516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187061525-A-C

http://identifiers.org/hco/1/GRCh38#217470006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187061000-C-A

217470006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187061000-C-T

217470492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187060522-T-C

217470507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187060507-G-C

217470775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187060243-T-C

217471526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187059464-G-T

217471588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187059408-A-G

217471646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187059350-G-C

217471727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187059260-A-T

217471912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187059082-G-C

217472067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187058954-T-G

217473447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187057922-T-G

217473506-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187057875-T-A

217473526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187057855-A-G

217474391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187056855-C-T

217474788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187056525-G-C

217474906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187056409-A-G

217475033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187056289-T-C

217475137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187056196-T-C

217491449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187054748-G-T

217491461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187054736-A-G

217491463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 187054734-T-G

217491617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 187054593-A-G

217491617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 187054593-A-T

217491621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 187054589-T-C

217491621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 187054589-T-G

217491787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187054440-A-G

http://identifiers.org/hco/1/GRCh38#217491821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187054405-A-C

217491821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187054405-A-G

217491947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 187054333-A-G

217492088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 187054234-A-G

217492260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 187054087-C-T

217492437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 187053909-T-C

217492437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 187053909-T-G

217492465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 187053882-G-T

217492480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 187053869-T-C

217492549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 187053809-G-T

217492568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 187053792-G-C

217492676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_retained_variant
orthologous variants: 187053688-C-T

217492908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187053491-G-A

217492934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187053470-A-G

217493188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187053269-T-C

217493352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187053103-C-G

217493352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187053103-C-T

http://identifiers.org/hco/1/GRCh38#217494299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187052235-C-A

217494299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187052235-C-G

217494925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187052041-A-G

217494944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187052023-G-C

http://identifiers.org/hco/1/GRCh38#217495102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187051894-C-A

217495102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187051894-C-T

217495115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187051882-C-T

217495143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187051852-G-A

217495143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187051852-G-T

217495148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187051847-A-G

217495338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187051672-A-G

217495381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187051638-T-C

217495496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187051540-C-T

217495677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187051348-T-C

217498131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187048917-A-G

217498131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187048917-A-T

217498168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187048880-C-T

217498247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 187048825-G-A

217498247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 187048825-G-T

217498260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 187048812-T-C

217498304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 187048782-A-T

217498563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 187048550-A-G

217498852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187048266-A-G

217498942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187048180-C-G

217498944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187048178-A-T

http://identifiers.org/hco/1/GRCh38#217499005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187048123-A-C

217499153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187048018-G-A

217499155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187048016-G-A

217499604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187047837-C-T

217499610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187047831-T-C

217499786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187047670-G-T

217499853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187047608-G-A

217503167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187046973-A-G

217503324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187046808-G-C

217503434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187046728-T-G

217503506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187046658-G-C

217503564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187046607-G-A

217503791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187046427-A-G

217503792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187046426-G-A

217503853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187046355-G-T

217504039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187046196-T-A

217504390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187045928-A-G

217504891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187045409-A-G

217504897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187045403-G-A

http://identifiers.org/hco/1/GRCh38#217504954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187045225-A-C

217505093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187045059-G-A

217506478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187044464-G-A

217506621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187044307-A-G

217506646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187044282-G-A

217507315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187043768-C-T

217507421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187043665-C-T

217507571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187043329-G-A

217507571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187043329-G-T

217507609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187043288-G-A

217507667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187043229-A-G

217507840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187043077-T-C

217508184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187042824-G-A

217508778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187041777-T-C

217509009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187041543-A-G

217514791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187036620-A-G

217514834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 187036580-G-A

217514834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 187036580-G-T

http://identifiers.org/hco/1/GRCh38#217514951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187036472-A-C

217515777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187036233-A-G

http://identifiers.org/hco/1/GRCh38#217516104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187035887-C-A

217516104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187035887-C-T

217516122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187035869-G-A

217516122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187035869-G-T

217517172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187034865-G-A

217517290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187034746-T-C

217518266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187033454-G-A

217518310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187033427-G-A

217518897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187032929-G-C

217518938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187032888-C-T

http://identifiers.org/hco/1/GRCh38#217518978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187032849-C-A

217519281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187032453-T-C

217522075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187032084-T-G

217522260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187031888-T-C

217522595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187031583-G-T

217522645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187031533-A-G

217522707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187031475-T-C

217522819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187031370-G-A

217522902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187031279-G-A

217522902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187031279-G-C

217523011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187031158-A-G

217523031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187031140-A-T

217523127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187030541-T-G

217525873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187029294-C-G

217525936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187029239-T-C

217525949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187029223-G-C

217526024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187029144-G-A

217526395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187028813-T-A

217528632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187026507-C-T

217528794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187026370-G-A

http://identifiers.org/hco/1/GRCh38#217530722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187026273-A-C

217530911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187026108-T-C

217534501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187025175-G-A

217536609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187022314-T-C

217537335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187021949-A-G

217537435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187021865-T-C

217537748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187021598-A-G

217538174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187021174-A-G

http://identifiers.org/hco/1/GRCh38#217538238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187021110-A-C

http://identifiers.org/hco/1/GRCh38#217538289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187021058-C-A

217538719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187020342-G-A

217538772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187020292-T-A

217538776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187020288-T-C

217539397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187019691-C-G

217539558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187019530-A-G

217539973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187019114-G-C

http://identifiers.org/hco/1/GRCh38#217540165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187018910-C-A

217540165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187018910-C-T

217545650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 187015171-T-C

217545844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187014985-C-T

217545930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187014899-T-C

217545930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187014899-T-G

217545967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187014864-T-C

217549051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187014522-G-A

217549076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187014497-C-T

217549083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187014490-T-C

217549112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187014466-A-G

217549327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187014104-T-A

217549799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187013711-C-T

217549844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187013664-T-C

217550927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187012927-T-A

217550960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187012892-G-A

217551167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187012722-T-A

217551435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187012483-G-A

217551593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187012368-T-G

217551642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187012310-C-G

217551642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187012310-C-T

http://identifiers.org/hco/1/GRCh38#217551654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187012269-A-C

http://identifiers.org/hco/1/GRCh38#217552128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187011870-C-A

217552416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187011673-T-C

http://identifiers.org/hco/1/GRCh38#217552697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187011417-C-A

217553150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187010963-C-T

217553246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187010872-A-G

217553284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187010837-T-C

217553371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187010748-A-G

217553815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187010305-T-C

217554056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187010067-G-A

217554329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187009794-A-T

217554547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187009607-T-G

217554610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187009552-T-C

217555054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187009158-G-C

217555724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187008517-T-C

217557611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187007324-T-A

217557611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187007324-T-G

217557632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187007304-A-T

217557956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187007020-C-T

http://identifiers.org/hco/1/GRCh38#217558658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187006401-A-C

http://identifiers.org/hco/1/GRCh38#217558696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187006371-C-A

217559420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187005701-A-G

217559661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187005344-C-T

217559721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187005284-G-A

217560961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187004810-T-C

217561858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187004578-A-G

217563009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187004171-C-T

217563471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187003734-G-A

217563560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187003664-C-T

217564239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187003335-C-T

217564606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187002966-A-G

217565482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187002472-T-C

217565627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187002344-T-C

217566388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187001968-G-C

217566500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187001871-A-T

217566593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187001786-A-T

217566595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187001784-T-A

217566627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187001763-T-A

217566689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187001699-G-C

217566736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187001653-C-T

217566771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187001626-G-A

http://identifiers.org/hco/1/GRCh38#217567749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187000989-A-C

http://identifiers.org/hco/1/GRCh38#217568639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187000451-A-C

217568662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187000435-A-G

217568974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187000137-T-C

http://identifiers.org/hco/1/GRCh38#217569101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#187000030-A-C

217569101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 187000030-A-T

217569340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186999806-A-G

217569912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186999489-T-C

217572723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186997564-A-G

217572859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186997430-G-T

217573237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186997061-C-T

217573293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186997006-G-A

217573988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186996321-T-G

217574036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186996273-C-T

217574116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186996193-C-T

217574196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186996118-A-G

217574210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186996104-G-A

217574235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186996081-T-C

217574261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186996039-T-A

217574261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186996039-T-C

217574278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186995982-T-C

217574320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186995933-C-T

217574613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186995673-C-T

http://identifiers.org/hco/1/GRCh38#217575094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186995144-A-C

217575199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186994961-T-C

217575206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186994954-T-A

217575481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186994674-A-G

217575529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186994626-T-C

217575609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186994549-G-A

217575860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186994299-T-C

217575954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186994202-A-G

217576006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186994151-G-C

217576009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186994148-A-G

217576134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186994030-C-T

217576498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186993678-T-C

217577305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186992866-T-C

217577353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186992823-C-G

http://identifiers.org/hco/1/GRCh38#217577355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186992821-C-A

217577366-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186992810-T-A

217577651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186992523-G-T

217577658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186992516-C-T

217577701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186992474-C-T

http://identifiers.org/hco/1/GRCh38#217578701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186992209-A-C

217579174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186991783-T-C

217579333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186991590-T-A

217579401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186991524-A-T

217579583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186991341-C-G

217579583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186991341-C-T

217579817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186991117-C-T

217579853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186991082-A-G

217579877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186991059-T-C

217579918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186991019-G-A

217579990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186990971-G-T

217580264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186990670-C-T

217580386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186990577-C-T

217580403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186990556-A-T

217580582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186990439-G-A

217580614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186990410-T-C

217580688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186990348-A-G

217580763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186990272-C-T

217582058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186989649-A-T

217582069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186989638-T-C

217582146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186989570-C-T

217582293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186989433-C-T

217582407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186989305-T-C

217582677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186989050-G-C

217589651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186984766-T-C

217589747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186984393-T-C

217589876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186984305-C-G

217589930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186984258-G-A

217591916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186982617-C-T

217592125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186982304-C-T

217592180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186982245-T-C

http://identifiers.org/hco/1/GRCh38#217592357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186982040-C-A

217592369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186982028-A-G

217592384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186982015-G-C

217592387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186982012-G-A

217592388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186982011-G-A

217592662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186981791-A-T

217592732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186981720-G-A

217592812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186981633-T-A

217592901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186981550-G-A

217593078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186981396-T-C

217593449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186981025-A-G

217594787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186979741-T-C

217594823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186979702-T-C

http://identifiers.org/hco/1/GRCh38#217594866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186979659-A-C

217595160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186979313-T-A

217595399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186979082-C-T

217595427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186979068-G-C

217595748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186978986-T-A

http://identifiers.org/hco/1/GRCh38#217596118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186978736-A-C

217596127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186978727-T-A

217596131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186978723-C-T

217596145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186978709-A-G

217596198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186978676-C-G

http://identifiers.org/hco/1/GRCh38#217596580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186978013-A-C

217596580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186978013-A-G

217597205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186977440-T-C

217597222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186977428-A-G

217597718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186977096-T-C

217597727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186977087-G-A

217597927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186976943-G-A

217598074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186976796-T-C

217598871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186976650-G-A

217598921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186976599-G-A

217599036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186976520-G-A

217599215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186976360-C-T

217599230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186976345-C-T

217599495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186976103-C-T

217599686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186975908-C-T

217599722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186975872-A-G

217599821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186975726-T-C

217599992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186975433-T-A

217599992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186975433-T-C

217599992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186975433-T-G

217600134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186975292-G-T

217600292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186975148-T-C

217600372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186975063-C-T

217600406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186975030-T-C

217600420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186975016-C-T

217600683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186974750-A-G

217601130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186974311-G-A

217601454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186973918-T-C

217601571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186973819-C-T

217601668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186973707-A-T

http://identifiers.org/hco/1/GRCh38#217601714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186973663-A-C

http://identifiers.org/hco/1/GRCh38#217601736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186973647-C-A

217601736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186973647-C-G

http://identifiers.org/hco/1/GRCh38#217601876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186973486-C-A

217601877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186973485-G-A

217602010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186973328-T-G

217602543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186972830-G-A

217602595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186972805-A-G

217603018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186972476-T-C

217603071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186972427-T-C

217603148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186972378-T-A

217603148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186972378-T-C

217603241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186972305-G-C

217603254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186972292-C-T

http://identifiers.org/hco/1/GRCh38#217603414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186972143-C-A

http://identifiers.org/hco/1/GRCh38#217605111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186971254-A-C

217605147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186971220-C-T

217605228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186971158-T-G

217606038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186969735-T-C

217606099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186969668-T-C

217607075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186968926-C-T

217607126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186968876-T-C

217607309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186968712-T-A

217607379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186968649-T-G

217607639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186968393-C-G

217607648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186968384-T-C

217607665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186968367-G-A

217607738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186968335-G-A

http://identifiers.org/hco/1/GRCh38#217607784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186968313-A-C

217607864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186968276-G-A

217608194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186968000-T-C

217608467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186967767-G-A

217608467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186967767-G-T

217608762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186967480-T-C

217608762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186967480-T-G

217608783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186967460-T-C

217608865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186967383-C-T

217608971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186967304-T-C

217609139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186967154-T-C

217609293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186967002-G-T

http://identifiers.org/hco/1/GRCh38#217609311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186966987-C-A

217609311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186966987-C-T

217609314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186966984-G-A

217609314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186966984-G-C

217609340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186966960-A-G

217609352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186966948-T-A

217609352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186966948-T-C

217609557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186966764-G-T

217609773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186966568-T-C

217609773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186966568-T-G

217609976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186966366-A-G

http://identifiers.org/hco/1/GRCh38#217609983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186966359-C-A

217609983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186966359-C-T

217609984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186966358-T-G

217609996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186966346-G-T

217610000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186966342-G-A

http://identifiers.org/hco/1/GRCh38#217610071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186966269-C-A

http://identifiers.org/hco/1/GRCh38#217610098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186966242-C-A

217610098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186966242-C-G

217610208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186966133-T-C

217610448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186965898-G-A

217610448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186965898-G-C

217610448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186965898-G-T

217610450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186965896-A-G

217610490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186965861-T-A

217610490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186965861-T-G

217610514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186965837-C-T

http://identifiers.org/hco/1/GRCh38#217610516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186965835-C-A

217610516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186965835-C-T

http://identifiers.org/hco/1/GRCh38#217610776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186965613-C-A

217610776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186965613-C-T

217610841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186965556-G-T

217611026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: missense variant
orthologous variants: 186965371-C-T

217611110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186965296-A-G

217611111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186965295-G-C

217611111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186965295-G-T

217612351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186964944-A-G

217612539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186964752-T-A

http://identifiers.org/hco/1/GRCh38#217612549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186964742-C-A

217612885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186964284-A-T

217612916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186964240-A-G

217613461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186963644-T-A

217613461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186963644-T-C

217614030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186963141-A-G

http://identifiers.org/hco/1/GRCh38#217614060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186963111-A-C

217614060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186963111-A-G

217614063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186963108-T-A

217614093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186963078-A-G

217614093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186963078-A-T

217614108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186963066-T-C

217614120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186963054-A-G

http://identifiers.org/hco/1/GRCh38#217614170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186963011-C-A

217614170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: missense variant
orthologous variants: 186963011-C-G

217614170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: missense variant
orthologous variants: 186963011-C-T

217614196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: synonymous variant
orthologous variants: 186962985-G-A

217614196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: synonymous variant
orthologous variants: 186962985-G-T

217614200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 186962981-T-C

http://identifiers.org/hco/1/GRCh38#217614232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186962944-C-A

217614232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186962944-C-T

217614253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186962925-A-G

http://identifiers.org/hco/1/GRCh38#217614313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186962868-C-A

217614313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186962868-C-G

217614313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186962868-C-T

217614332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186962849-T-A

217614332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186962849-T-C

217614332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186962849-T-G

217614738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186962427-A-G

217614907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186962291-T-C

217614969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186962222-G-A

217614979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186962217-A-G

217615113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186962061-A-G

217615140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186962006-T-C

217615205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186961920-T-C

217615927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186961045-C-T

217616110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186960914-T-C

217616465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186960799-G-C

217616516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186960762-C-T

217616517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186960761-C-T

217616762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186960545-G-A

217616762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186960545-G-T

217616805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186960514-A-T

217617467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186959999-T-C

217617806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186959687-G-A

217617854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186959644-T-C

http://identifiers.org/hco/1/GRCh38#217617877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186959617-A-C

217617962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186959538-A-G

http://identifiers.org/hco/1/GRCh38#217619353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186958832-A-C

217619585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186958636-T-C

217619597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186958624-A-G

http://identifiers.org/hco/1/GRCh38#217619622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186958598-A-C

217619773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186958424-T-C

217619929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: synonymous variant
orthologous variants: 186958268-G-T

217620137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: missense variant
orthologous variants: 186958060-C-T

217620464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: missense variant
orthologous variants: 186957733-T-A

217620677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186957513-T-C

217620682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186957508-T-C

217620682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186957508-T-G

217620955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, undefined
orthologous variants: 186956838-G-C

217621028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, undefined
orthologous variants: 186956801-A-G

217621159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, undefined
orthologous variants: 186956674-T-A

217621207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186956650-G-A

217621358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186956548-A-G

217621364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186956542-G-A

217621369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186956537-C-T

217621684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186956123-C-G

217621922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186955913-A-G

217621941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186955904-G-A

217621959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186955886-G-T

217622180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186955695-A-G

217622268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186955617-G-A

217622598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186955391-C-T

http://identifiers.org/hco/1/GRCh38#217622636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186955359-C-A

217622803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186955258-C-T

217623092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186955046-T-C

http://identifiers.org/hco/1/GRCh38#217624588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186953823-C-A

217624902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186953551-A-T

217625374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186953177-C-T

217625552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186952977-T-C

217625598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186952944-C-T

217626123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186952712-C-T

217626329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186952297-A-G

217626583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186952014-A-G

217627943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186950899-C-G

217628016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186950857-A-G

217628084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186950801-C-T

217628378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186950556-A-G

http://identifiers.org/hco/1/GRCh38#217628468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186950472-A-C

217628860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186950206-G-C

217629153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186949928-T-C

217629381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186949349-T-C

217629486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186949205-T-C

217629663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186949033-A-G

217629712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186948983-G-A

217629736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186948959-T-A

217629736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186948959-T-C

217629902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186948577-G-C

217630325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186948210-T-C

217630470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron variant
orthologous variants: 186948085-G-A

http://identifiers.org/hco/1/GRCh38#217630875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#186947899-C-A

217630875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, undefined
orthologous variants: 186947899-C-G

217630875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25499
most severe consequence: intron_variant, undefined
orthologous variants: 186947899-C-T