9910918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67579526-T-C

http://identifiers.org/hco/17/GRCh38#9911000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67579444-C-A

http://identifiers.org/hco/17/GRCh38#9911026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67579418-C-A

9911026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67579418-C-G

9911040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67579406-G-A

9911079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67579354-G-A

9911079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67579354-G-C

9911083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67579350-T-G

9911232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67579248-A-G

9911235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67579245-G-A

9911235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67579245-G-T

9911280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67579207-G-T

http://identifiers.org/hco/17/GRCh38#9911406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67579115-C-A

9911619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578966-G-A

9911632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578953-C-G

9911710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578887-G-A

9911741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578855-C-G

9911741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578855-C-T

http://identifiers.org/hco/17/GRCh38#9911762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67578835-C-A

9911762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578835-C-T

http://identifiers.org/hco/17/GRCh38#9911778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67578819-C-A

9911778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578819-C-T

9911787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578815-A-G

9911829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578776-C-T

9911830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578775-G-A

9911830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578775-G-T

9911911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578697-G-A

9911911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578697-G-C

9911911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578697-G-T

http://identifiers.org/hco/17/GRCh38#9911922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67578686-A-C

9911933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578675-G-T

http://identifiers.org/hco/17/GRCh38#9911983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67578636-C-A

9911983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578636-C-T

9912059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578545-G-T

9912070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578536-T-C

9912075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578531-A-G

9912212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578430-A-G

9912252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578409-T-C

9912329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578336-G-T

9912330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578335-G-A

9912333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578332-G-A

http://identifiers.org/hco/17/GRCh38#9912493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67578227-C-A

9912493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578227-C-G

9912493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578227-C-T

9912516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578206-G-A

9912516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578206-G-T

9912517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578205-T-C

9912526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578196-G-T

9912561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578159-C-T

http://identifiers.org/hco/17/GRCh38#9912623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67578112-C-A

http://identifiers.org/hco/17/GRCh38#9912646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67578098-C-A

9912721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578050-T-A

9912721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67578050-T-G

9912821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577913-T-C

9912838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577896-A-G

9912848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577886-G-A

9912848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577886-G-T

9912961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577826-G-A

9912961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577826-G-C

9913063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577735-T-C

9913063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577735-T-G

9913092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577713-T-A

9913092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577713-T-C

9913246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577619-G-T

9913257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577608-G-A

9913276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577589-T-C

9913277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577588-G-T

9913278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577587-A-G

http://identifiers.org/hco/17/GRCh38#9913618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67577280-C-A

9913618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577280-C-G

9913618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577280-C-T

9913630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577268-C-G

9913666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577232-A-G

http://identifiers.org/hco/17/GRCh38#9913709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67577197-C-A

9913709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577197-C-T

http://identifiers.org/hco/17/GRCh38#9913818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67577093-C-A

9913818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577093-C-T

9913877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577028-T-C

9913892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67577012-G-T

9914564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67576623-T-C

9914586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67576601-G-A

9914586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67576601-G-T

9914595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67576594-G-A

9914595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67576594-G-T

9914685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67576527-A-G

9914697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67576515-G-A

9914697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67576515-G-T

9914765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67576440-A-G

9914829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67576383-G-T

9914982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67576149-T-C

9914984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67576147-A-G

9915041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67576084-A-G

9915082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67576037-G-C

9915082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67576037-G-T

9915090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67576029-G-A

http://identifiers.org/hco/17/GRCh38#9915191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67575954-C-A

9915354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575797-C-T

9915401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575743-T-C

9915509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575684-G-T

http://identifiers.org/hco/17/GRCh38#9915522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67575671-A-C

9915522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575671-A-G

9915650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575558-C-G

9915650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575558-C-T

9915651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575557-G-A

9915768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575439-T-A

9915778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575424-G-A

9915778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575424-G-C

9916063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575354-T-C

9916072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575345-A-G

9916100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575322-G-A

9916198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575239-G-A

9916198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575239-G-T

9916283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575180-G-A

9916283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575180-G-C

9916283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575180-G-T

9916293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575172-C-T

9916316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575153-G-A

9916465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67575037-A-G

9916501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67574998-G-A

9916501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67574998-G-T

9916511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67574988-T-G

9916677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67574816-G-T

http://identifiers.org/hco/17/GRCh38#9916804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67574691-C-A

9916804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67574691-C-T

http://identifiers.org/hco/17/GRCh38#9916826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67574671-C-A

9916827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67574670-T-C

9916865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67574632-G-A

9916865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67574632-G-T

9916928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3 prime UTR variant
orthologous variants: 67574570-A-G

9917010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 67574483-C-G

9917015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 67574478-A-G

9917028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67574465-T-A

9917028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67574465-T-C

9917063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67574430-A-G

9917071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67574422-G-C

9917071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67574422-G-T

http://identifiers.org/hco/17/GRCh38#9917107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67574392-C-A

9917107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67574392-C-G

9917208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67574295-C-T

9917456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67574046-G-A

9917456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67574046-G-T

9917482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67574023-T-A

http://identifiers.org/hco/17/GRCh38#9917868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67573686-C-A

9917868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67573686-C-T

http://identifiers.org/hco/17/GRCh38#9917923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67573640-A-C

9917923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67573640-A-T

9917928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67573635-G-A

9917928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67573635-G-C

9917928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67573635-G-T

9917954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67573603-C-T

http://identifiers.org/hco/17/GRCh38#9917969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67573591-C-A

9917969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67573591-C-T

9918094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67573464-T-C

9918103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 67573455-C-T

9918154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67573404-T-A

9918154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67573404-T-C

9918154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67573404-T-G

9918188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67573356-G-A

9918188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67573356-G-T

http://identifiers.org/hco/17/GRCh38#9918231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67573314-A-C

9918960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67572766-C-T

9919204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67572558-C-T

9919260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67572493-G-A

9919281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67572472-G-A

9919413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67572338-T-C

9919424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67572327-A-G

9919502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67572252-A-G

9919735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67572019-A-G

9919736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67572018-G-A

9919736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67572018-G-T

http://identifiers.org/hco/17/GRCh38#9919763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67571985-C-A

9919763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67571985-C-T

9919792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67571953-C-T

9919828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67571928-T-A

9919828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67571928-T-C

http://identifiers.org/hco/17/GRCh38#9920740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67571048-C-A

9920800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67570988-C-G

9920800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67570988-C-T

9920873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67570906-G-C

9921042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67570743-C-T

9921046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67570739-G-A

9921113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67570675-C-T

9921467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67570602-G-A

9922184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67570222-T-C

9922193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67570213-T-C

9923517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67568262-A-G

9923615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67568145-C-T

9923650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67568111-A-G

9923741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67568024-C-T

9923989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67567785-T-A

9924581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67567490-T-A

http://identifiers.org/hco/17/GRCh38#9924814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#67567296-C-A

9924814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67567296-C-T

9924827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67567282-G-A

9924830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67567279-G-A

9924870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67567257-A-G

9925240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67566692-C-G

9925417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67566576-G-A

9925417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67566576-G-T

http://identifiers.org/hco/17/GRCh38#9925421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67566572-C-A

9925421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67566572-C-G

9925421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67566572-C-T

9925650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67566370-G-A

9925650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67566370-G-T

9925961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67565836-C-T

9925982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67565814-C-T

9925998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67565798-C-G

9926011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67565794-G-A

9926055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67565723-C-G

9926071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67565707-G-T

9926450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67565336-G-A

http://identifiers.org/hco/17/GRCh38#9926513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67565289-C-A

9926513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67565289-C-T

9926521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67565284-C-T

http://identifiers.org/hco/17/GRCh38#9926522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67565283-C-A

9926522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67565283-C-T

http://identifiers.org/hco/17/GRCh38#9926524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67565281-C-A

9926526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67565279-A-G

9926556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67565263-T-C

9926566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67565251-G-A

9926566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67565251-G-T

http://identifiers.org/hco/17/GRCh38#9926576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67565241-C-A

9926578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67565239-G-A

9926578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67565239-G-T

9926663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67565168-C-T

9926747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67565084-G-A

9926799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67565030-G-A

9926799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67565030-G-T

http://identifiers.org/hco/17/GRCh38#9926808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67565022-C-A

9926808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67565022-C-T

9930069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67564381-C-T

9930135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67564316-T-C

9930183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67564266-T-C

9930486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67563990-G-A

9930492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67563980-G-T

9930591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67563880-T-C

9930787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67563682-C-T

9930792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67563677-A-G

9930814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67563655-C-T

9930846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67563623-G-A

9930856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67563613-A-G

http://identifiers.org/hco/17/GRCh38#9930861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67563608-C-A

9930882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67563592-C-T

9930965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67563476-C-T

9931019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67563434-G-A

9931633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67563221-T-C

9931789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67563085-C-T

9931807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67563071-T-C

9931919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67562919-A-G

9932711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67562437-T-C

9934034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67561594-T-G

http://identifiers.org/hco/17/GRCh38#9934077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67561571-C-A

9934077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67561571-C-T

9934082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67561566-G-A

9934082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67561566-G-T

9934151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67561509-G-A

9934151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67561509-G-T

http://identifiers.org/hco/17/GRCh38#9934317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67561315-C-A

9935828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67560536-G-T

9936097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67559722-A-G

9936248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67559609-T-C

9936889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67558983-T-C

9936918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67558954-G-C

9937624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67558418-T-C

9937671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67558374-G-A

9937803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67558271-C-T

9937891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67558203-T-A

9938059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67558073-A-G

http://identifiers.org/hco/17/GRCh38#9938082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67558051-C-A

9938082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67558051-C-T

9938794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67557515-C-T

9939062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67557267-T-C

9939394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67556965-T-C

http://identifiers.org/hco/17/GRCh38#9939429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67556937-C-A

9939429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67556937-C-T

9939712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67556731-C-T

9939917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67556564-T-A

http://identifiers.org/hco/17/GRCh38#9939983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67556478-C-A

9939983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67556478-C-T

9940091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67556334-T-G

http://identifiers.org/hco/17/GRCh38#9940218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67556194-C-A

9940218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67556194-C-T

9940410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67556112-T-C

9940876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67555715-T-C

http://identifiers.org/hco/17/GRCh38#9940900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67555692-C-A

9940900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67555692-C-T

9940921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67555672-C-T

9940961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67555636-T-C

9941098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67555556-G-C

9941203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67555475-C-T

9941245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67555442-C-G

9941392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67555314-T-C

9941438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67555271-T-C

http://identifiers.org/hco/17/GRCh38#9941484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67555232-C-A

9941578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67555150-C-T

9941614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67555089-C-T

9941634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67555069-G-C

9941666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67555038-T-C

http://identifiers.org/hco/17/GRCh38#9942442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67553908-A-C

http://identifiers.org/hco/17/GRCh38#9942453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67553897-A-C

9942453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67553897-A-G

9942542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67553818-A-G

9942542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67553818-A-T

9942580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67553779-G-C

9942583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67553776-T-A

9942583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67553776-T-C

9942583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67553776-T-G

9942678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67553527-A-G

9942772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67553451-C-G

9942807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67553423-G-C

9942826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67553404-G-A

9942862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67553391-G-A

9943019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67553172-G-A

9943019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67553172-G-T

9943103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67553008-G-T

9943186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67552925-T-C

9943186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67552925-T-G

9944474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67552844-G-C

9944617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67552732-C-T

9944618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67552731-G-A

9944639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67552710-G-A

9944658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67552691-T-C

9944676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67552673-A-G

9944710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67552627-G-C

http://identifiers.org/hco/17/GRCh38#9944863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67552496-A-C

9945210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67552091-C-G

9945292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67552018-T-A

9945292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67552018-T-C

http://identifiers.org/hco/17/GRCh38#9945295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67552015-A-C

9945324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67551988-T-C

9945369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67551943-A-G

9945369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67551943-A-T

9945402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67551913-C-T

9945427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67551895-G-A

9945439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67551883-C-T

9946054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67551668-G-T

9946055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67551667-A-G

9946359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67551381-C-T

9946629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67551150-G-C

9946790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67551008-A-G

9946790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67551008-A-T

http://identifiers.org/hco/17/GRCh38#9946828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67550992-C-A

9946828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67550992-C-T

9946837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67550984-G-A

9946837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67550984-G-T

http://identifiers.org/hco/17/GRCh38#9946848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67550973-C-A

9946860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67550965-G-A

9946860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67550965-G-T

9946874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67550952-G-A

9946874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67550952-G-T

http://identifiers.org/hco/17/GRCh38#9953982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67548305-A-C

9954095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67548203-G-T

9954751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67547913-G-T

http://identifiers.org/hco/17/GRCh38#9954809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67547862-C-A

9955188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67547552-A-G

9955290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67547445-T-C

9955419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67547301-T-C

9955901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67546816-C-T

http://identifiers.org/hco/17/GRCh38#9955902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67546815-C-A

http://identifiers.org/hco/17/GRCh38#9956133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67546636-A-C

9956155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67546625-C-T

9956177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67546612-G-T

9956595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67546242-G-C

9956699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67546157-G-A

9956699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67546157-G-T

http://identifiers.org/hco/17/GRCh38#9956758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67546092-A-C

9956765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67546086-G-T

9956898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67545968-T-C

9956948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67545918-G-A

9956980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67545880-C-G

9956989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67545871-T-C

9957034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67545823-C-T

9957184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67545719-T-C

9957184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67545719-T-G

9957314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67545594-T-C

9957364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67545548-G-A

9957410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67545526-C-T

9957855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67545156-T-C

9958046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67544947-T-C

9958259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67544740-A-G

9958306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67544697-C-T

9958550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67544444-G-A

9958790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67544145-T-G

http://identifiers.org/hco/17/GRCh38#9958837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67544097-A-C

9958873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67544061-T-A

9958873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67544061-T-C

9958873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67544061-T-G

http://identifiers.org/hco/17/GRCh38#9958913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67544022-C-A

9958913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67544022-C-T

9958997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67543934-A-T

9959105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67543836-T-C

http://identifiers.org/hco/17/GRCh38#9959132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67543809-C-A

9959132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67543809-C-T

9959236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67543702-G-A

9959236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67543702-G-T

9959263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 67543675-G-A

9959327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67543609-C-G

9959327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67543609-C-T

http://identifiers.org/hco/17/GRCh38#9959404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67543505-C-A

9959473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 67543440-C-T

9959569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67543346-T-A

http://identifiers.org/hco/17/GRCh38#9959642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#67543258-A-C

9959642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67543258-A-G

9959642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67543258-A-T

9959737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67543163-C-T

9959856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67543071-A-G

9959859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67543068-G-A

9959894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67543033-G-A

http://identifiers.org/hco/17/GRCh38#9959931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67543003-C-A

9959931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67543003-C-T

9961198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67542283-T-C

9961221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67542260-T-C

9961221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67542260-T-G

http://identifiers.org/hco/17/GRCh38#9961348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67542106-A-C

http://identifiers.org/hco/17/GRCh38#9961610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67541852-C-A

9961610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67541852-C-T

9962613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67541537-A-G

9962697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67541461-A-T

9962779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67541383-G-A

9962908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67541267-G-A

9963073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67541106-T-A

9963104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67541075-C-T

9963146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67541042-T-C

9963193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67540993-C-G

9963194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67540992-T-C

9963228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67540965-G-T

9963584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67540418-G-A

9963951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67540078-T-G

9963998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67540031-G-A

9964084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67539942-G-A

9964612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67539376-T-A

9964612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67539376-T-C

9964656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67539313-T-C

9964714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67539235-G-A

http://identifiers.org/hco/17/GRCh38#9964762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67539192-A-C

9964994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67539002-G-T

9965751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67538838-C-T

http://identifiers.org/hco/17/GRCh38#9965766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67538821-C-A

9967597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67536757-A-G

9967886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67535609-T-C

9968085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67535422-G-T

9968345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67535339-T-C

http://identifiers.org/hco/17/GRCh38#9968356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67535328-C-A

9968382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67535312-C-T

9968968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67534957-A-G

9968968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67534957-A-T

9969024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67534819-C-T

9969626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67534236-T-C

9969792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67534075-T-C

9969816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67534051-C-T

http://identifiers.org/hco/17/GRCh38#9969833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67534034-C-A

9969833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67534034-C-T

9969865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67534000-G-A

9969865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67534000-G-T

9969868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67533997-A-G

9969873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67533992-T-C

http://identifiers.org/hco/17/GRCh38#9969901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67533965-C-A

9969901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67533965-C-G

9970127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67533790-G-A

9970127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67533790-G-C

9970142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67533779-G-A

9970142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67533779-G-C

9970295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67532337-T-C

9970571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67532048-G-T

9972534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67529379-G-A

http://identifiers.org/hco/17/GRCh38#9972585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67529328-C-A

9973234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67528629-G-A

9973896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67528141-G-C

9973928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67528108-C-T

9974110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67527914-C-T

9974338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67527690-A-G

9974365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67527676-C-G

http://identifiers.org/hco/17/GRCh38#9974521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67527524-A-C

9974551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67527498-T-C

http://identifiers.org/hco/17/GRCh38#9974625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67527427-A-C

9974625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67527427-A-G

http://identifiers.org/hco/17/GRCh38#9974836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67527236-C-A

9975062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67527016-G-A

9975458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67526874-C-T

9975474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67526847-G-C

9975474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67526847-G-T

9975489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67526831-C-T

9975513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67526806-C-T

9975530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67526790-C-T

9975584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67526734-T-A

9975584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67526734-T-G

http://identifiers.org/hco/17/GRCh38#9975809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67526512-C-A

9975836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67526480-G-A

9976043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67526293-G-A

http://identifiers.org/hco/17/GRCh38#9976333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67526032-A-C

9976401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67525970-C-T

9976424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67525941-G-C

9976509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67525878-C-G

9976567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67525827-C-T

9976586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67525814-G-A

9976586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67525814-G-C

9976800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67525604-T-C

9976802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67525599-G-C

9976838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67525548-A-G

9976841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67525545-C-T

9976862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67525524-C-T

9977402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67525115-C-T

9977412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67525104-T-C

9977818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67524742-C-T

9981436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67520858-T-C

9981461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67520833-G-A

9981762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67520556-C-G

http://identifiers.org/hco/17/GRCh38#9981814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67520504-C-A

9981814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 67520504-C-T

http://identifiers.org/hco/17/GRCh38#9981952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67520372-C-A

9981952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67520372-C-G

9981952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67520372-C-T

9981982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67520338-G-T

http://identifiers.org/hco/17/GRCh38#9982017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67520301-C-A

9982017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67520301-C-T

9985976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67519671-C-T

http://identifiers.org/hco/17/GRCh38#9986043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67519638-C-A

9986152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67519548-C-T

9986186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67519514-T-C

9986253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67519413-A-G

9986723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67518785-T-C

9987172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67518372-G-A

9987767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67517897-C-T

9987820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67517844-G-A

9988269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67517265-T-C

9988375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67517124-T-C

9988437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67517027-T-G

9988439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67517025-A-G

9991685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67513763-C-T

9991707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67513741-G-A

9991841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67513599-G-A

9992053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67513385-G-A

9992189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67513273-C-G

9992321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67513103-G-A

http://identifiers.org/hco/17/GRCh38#9998788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67510360-A-C

9998857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67510311-G-T

9999064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67510133-A-T

9999939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67509543-T-C

10000012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67509464-A-G

10000087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67509424-G-C

10000272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67509351-T-C

10000462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67509190-C-T

10000478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67509174-C-T

10000606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67508338-G-A

10000623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67508321-T-C

10000624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67508320-T-C

10003598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67508161-T-C

10003879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67507921-G-T

10003960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67507843-T-C

10004009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67507795-C-T

http://identifiers.org/hco/17/GRCh38#10004015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67507789-A-C

10004247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67507567-A-T

10004365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67507443-T-C

10004375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67507424-G-A

10004390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67507400-G-A

10004390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67507400-G-C

10004390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67507400-G-T

http://identifiers.org/hco/17/GRCh38#10004520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67507282-C-A

10004611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67507188-C-G

10004611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67507188-C-T

10005542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67506491-C-T

10005671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67506385-T-A

10005671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67506385-T-G

10007233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67503998-T-C

10007652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67503900-A-G

10007959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67503595-T-C

10008013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67503540-T-A

10008014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67503539-G-A

10008014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67503539-G-T

10008065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67503490-C-T

10008125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67503436-C-T

10008376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67503227-T-C

10008730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67502784-T-C

10008850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67502695-C-T

10008936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67502606-A-T

10009384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67502456-T-C

10012172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67501092-G-C

10012777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67500534-A-G

10013366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67500282-C-G

10013467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67500175-A-T

10013545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67500101-G-A

10013625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67500005-C-T

10013662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67499963-C-T

10013785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67499830-C-T

10013802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67499813-A-G

10014193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67499403-A-G

10014668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67498948-C-T

10015176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67498763-A-G

10018237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67495828-G-A

10018302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67495731-C-T

10018515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67495511-C-T

10018799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67495211-G-A

10018891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67495127-T-C

10019124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67494936-G-A

10019254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67494568-C-G

10019334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67494490-G-A

10019360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67494464-T-G

10019627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67494256-A-G

10019699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67494128-A-G

10019699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67494128-A-T

10019872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67493957-G-A

http://identifiers.org/hco/17/GRCh38#10019984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67493862-C-A

10019984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 67493862-C-G

10019984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 67493862-C-T

10020074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67493811-T-C

10020172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67493776-T-C

10020206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67493742-G-T

10020222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67493723-G-A

10020223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67493722-G-A

10020223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67493722-G-C

10020223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67493722-G-T

10020254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67493693-A-T

10020262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67493671-A-G

10020348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67493577-T-C

10020349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67493576-C-T

10020507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67493439-C-T

10020961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67493331-G-A

10020961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67493331-G-C

10021111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67493182-G-C

http://identifiers.org/hco/17/GRCh38#10021219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67493084-A-C

10021389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67492919-G-T

10021541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67492792-T-C

10021671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67492661-T-A

10021671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67492661-T-C

10021676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67492656-C-G

10021783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67492560-G-T

10021824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67492522-G-A

10021824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67492522-G-C

10022386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67492240-G-A

10022386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67492240-G-T

10022471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67492147-G-T

10022611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67492010-T-A

10022611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67492010-T-C

10022741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67491840-G-A

http://identifiers.org/hco/17/GRCh38#10023063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67491466-A-C

10023167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67491378-A-T

10023397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67491102-A-G

10023564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67490938-T-C

10023631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67490871-G-C

10023643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67490859-C-T

10023690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67490820-G-A

10023690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67490820-G-T

10023803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67490692-T-G

10024107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67490393-G-C

10024119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67490381-G-A

10024397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67489717-G-A

10024479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67489640-G-A

10024583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67489541-G-A

10024611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67489513-G-A

10024913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67488860-A-G

10025480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67488358-C-T

10025691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67488133-A-G

10025706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67488113-T-A

10025706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67488113-T-C

10025761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67487941-G-A

http://identifiers.org/hco/17/GRCh38#10025948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67487708-C-A

10025962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67487694-C-G

http://identifiers.org/hco/17/GRCh38#10026024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67487633-A-C

10026024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67487633-A-T

http://identifiers.org/hco/17/GRCh38#10026066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67487591-C-A

10026100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67487556-T-C

http://identifiers.org/hco/17/GRCh38#10026190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67487482-A-C

http://identifiers.org/hco/17/GRCh38#10026247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67487426-C-A

http://identifiers.org/hco/17/GRCh38#10026263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67487410-C-A

http://identifiers.org/hco/17/GRCh38#10026338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67487335-A-C

http://identifiers.org/hco/17/GRCh38#10026357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67487315-A-C

10026375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67487297-G-A

10026375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67487297-G-T

10026404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67487268-T-C

10026492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67487181-T-C

http://identifiers.org/hco/17/GRCh38#10026889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67486698-C-A

http://identifiers.org/hco/17/GRCh38#10027054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67486551-C-A

http://identifiers.org/hco/17/GRCh38#10027196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67486407-C-A

10027230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67486373-G-C

10030239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67483215-A-G

10030239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67483215-A-T

10030410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67483076-G-A

10031800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67482799-G-A

http://identifiers.org/hco/17/GRCh38#10032215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67482463-A-C

10032648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67481722-T-C

10033980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67479691-C-G

10034039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67479636-G-A

10034039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67479636-G-T

10034747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67479254-C-T

10035053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67478965-C-T

10035144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67478876-T-C

10035407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67478625-G-A

10035535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67478488-G-A

10035831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67478231-C-T

10035885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67478174-G-A

10035899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67478159-A-G

http://identifiers.org/hco/17/GRCh38#10036352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67477711-A-C

10036352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67477711-A-T

10036441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67477632-G-A

10036487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67477589-G-A

http://identifiers.org/hco/17/GRCh38#10036585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67477493-C-A

10036585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67477493-C-T

10036794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67477294-A-G

http://identifiers.org/hco/17/GRCh38#10036828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67477258-A-C

10036836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67477250-G-T

10037239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67476948-G-A

10037300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67476885-G-A

10038984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67475199-A-G

10039228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67474994-A-T

10042474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67472803-G-C

10042580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67472696-T-C

10042666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67472609-G-C

10042799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67472482-T-A

10042799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67472482-T-C

10046145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67470975-T-C

10046266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67470884-T-C

10048935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67469350-T-G

10050398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67469262-T-C

10050488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67469180-T-C

10050945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67468796-G-C

http://identifiers.org/hco/17/GRCh38#10051094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67468670-C-A

10051094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67468670-C-T

10051630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67468084-C-T

10051686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67468030-T-G

10051770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67467966-A-G

10051813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67467965-T-G

10051836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67467939-G-A

10051918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67467860-T-A

10052079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67467706-T-C

10052366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 67467568-G-A

10052424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 67467511-A-G

10052590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67467355-C-T

10052592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67467353-G-A

10052592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67467353-G-C

10052615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67467331-G-A

10052665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67467273-C-T

10052738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67467209-G-C

10052976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67466933-A-T

10053098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67466698-A-G

10053266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67466510-C-T

10053473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67466169-C-T

10054365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67465187-T-G

10054366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67465186-C-G

10054457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67465089-A-G

10054591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67464864-G-A

10054778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67464713-C-G

10054778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67464713-C-T

10054779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67464712-G-A

10054838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67464651-A-T

10055259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67464398-G-A

10055259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67464398-G-C

10055763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67463873-C-T

10055845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67463802-T-C

10058352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67463389-C-T

10058447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67463292-G-A

10058557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67463178-G-C

10058769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67462987-T-C

http://identifiers.org/hco/17/GRCh38#10058803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67462953-A-C

10058842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67462907-A-G

10059091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67462661-A-G

10059292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67462491-C-G

http://identifiers.org/hco/17/GRCh38#10059542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67462278-A-C

10059542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67462278-A-G

10059542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67462278-A-T

http://identifiers.org/hco/17/GRCh38#10059563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67462258-C-A

10059563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67462258-C-G

10059563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67462258-C-T

10059762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67462104-C-G

10059863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67462002-C-T

10059867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67461998-G-A

10059867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67461998-G-T

10060337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67461511-G-A

10060652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67461232-T-G

10061032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67460151-G-C

10061096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67460087-T-C

10061123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67460060-G-A

http://identifiers.org/hco/17/GRCh38#10061324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67459853-A-C

10061324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 67459853-A-G

10061325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 67459852-G-A

10061325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 67459852-G-T

10061358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 67459820-G-A

10061358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 67459820-G-T

10061382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67459797-G-T

http://identifiers.org/hco/17/GRCh38#10061395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67459784-C-A

10061395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67459784-C-T

10061452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67459728-A-G

http://identifiers.org/hco/17/GRCh38#10061486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67459694-C-A

10061595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67459583-T-C

http://identifiers.org/hco/17/GRCh38#10061624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67459554-A-C

10061627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67459551-A-T

10061628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67459550-T-G

10061760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67459439-C-T

10062814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67458376-T-C

10063051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67458160-C-T

10063222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67457623-A-G

10063312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67457519-G-A

10063352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67457491-C-T

10064217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67456395-C-G

10064311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67456300-T-G

10064503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67456125-G-A

http://identifiers.org/hco/17/GRCh38#10064533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67456100-A-C

10064615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67456013-A-G

10067826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67454365-A-G

http://identifiers.org/hco/17/GRCh38#10067840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67454360-C-A

10067840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67454360-C-T

10068169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67454073-C-T

10068195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67454049-G-A

10068345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67453957-G-A

10068345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67453957-G-C

10068548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67453771-G-C

10068837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67453503-A-G

10068946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67453373-G-A

10068946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67453373-G-T

10069009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67453307-G-A

10069009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67453307-G-C

http://identifiers.org/hco/17/GRCh38#10069213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67453086-C-A

10069344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67452655-C-G

10069360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67452642-G-C

10069477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67452525-C-T

10069512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67452490-G-C

10069585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67452409-C-T

10069876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67452136-C-G

10069876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67452136-C-T

http://identifiers.org/hco/17/GRCh38#10069968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67452046-C-A

10070567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67451354-T-C

10070698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67451231-C-T

10070807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67451116-C-T

10070809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67451114-G-A

10070861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67451092-G-A

10070932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67451039-A-T

10071103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67450890-G-C

10071210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67450787-G-A

10072474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67450447-G-A

10072500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67450421-C-T

http://identifiers.org/hco/17/GRCh38#10072685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67450204-C-A

10072685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67450204-C-T

10072693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67450196-A-G

10072970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67449935-A-G

10073187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67449732-G-A

10073458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67449478-G-C

10073459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67449477-C-T

10073596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67449347-C-T

10073666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67449268-G-C

http://identifiers.org/hco/17/GRCh38#10073689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67449245-C-A

10073779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67449173-G-C

http://identifiers.org/hco/17/GRCh38#10073932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67449027-C-A

10073932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67449027-C-T

10074104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67448833-G-A

10074206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67448699-T-C

10074240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67448668-C-T

10074733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67448187-T-C

10074950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67447955-T-A

10074950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67447955-T-C

10084232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67441627-G-C

10084333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67441523-T-A

10084333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67441523-T-C

10084357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67441499-T-C

10084364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67441492-C-G

10085077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67441133-C-T

10085286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67440930-A-T

10085290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67440926-T-C

10086056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67440548-C-G

10086111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67440490-G-A

10086121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67440480-G-C

10086123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67440478-G-A

10086123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67440478-G-C

10086362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67440237-G-A

10086560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67440084-G-A

10086749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67439910-G-A

10086749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67439910-G-C

http://identifiers.org/hco/17/GRCh38#10086810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67439847-A-C

10086830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67439827-C-G

10086830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67439827-C-T

http://identifiers.org/hco/17/GRCh38#10087517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67439043-A-C

10087691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67438755-T-G

10087771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67438675-A-G

10087798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67438625-C-G

10087913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67438502-C-T

10088277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67438036-G-A

10088446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67437882-G-T

10088520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67437816-T-C

10090214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67436537-G-A

10090378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67436371-T-C

10090415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67436336-T-A

10090520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67436247-G-A

10090561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67436123-T-C

10090598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67436086-T-A

http://identifiers.org/hco/17/GRCh38#10090952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67435749-C-A

10090952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67435749-C-T

10090960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67435741-G-T

10091048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67435510-A-G

10091091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67435447-C-T

10091261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67435285-T-C

10091302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67435239-T-C

10091310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67435231-G-A

10091374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67435178-G-A

10091378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67435174-T-C

10094013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67434567-T-A

10094039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67434535-G-C

10094256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67434344-A-G

10096542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67432337-T-A

10096693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67432222-T-C

10096778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67432114-T-A

10096792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67432099-T-A

10096792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67432099-T-C

10096918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67431979-C-T

10097139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67431619-A-G

10097151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67431607-G-C

10097204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67431533-T-C

10097278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67431454-C-G

10097598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67430534-T-C

10098473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67429971-A-G

10098578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67429885-A-G

10099238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67429594-A-G

10099291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67429526-G-A

10099476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67429332-C-T

10099482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67429326-G-A

10099540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67429258-A-G

10099596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67429222-T-G

10099639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67429179-C-G

10099934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67428903-C-T

10099939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67428898-G-A

http://identifiers.org/hco/17/GRCh38#10099976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67428848-A-C

10099976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67428848-A-G

10100132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67428679-C-T

10100499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67428317-C-T

10100581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67428244-G-T

10100635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67428171-T-C

10100709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67428114-C-T

10101112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67427624-A-T

http://identifiers.org/hco/17/GRCh38#10101383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67427369-C-A

10101383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67427369-C-T

10101468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67427297-C-T

10101747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67427044-C-T

10101760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67427031-G-A

http://identifiers.org/hco/17/GRCh38#10101802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67426997-C-A

10101802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67426997-C-G

10101802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67426997-C-T

10101986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67426837-T-C

10101986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67426837-T-G

10102498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67426667-G-A

10102498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67426667-G-C

10102522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67426643-A-G

10102583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67426583-G-C

10102682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67426483-A-G

10102696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67426473-A-T

10102724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67426449-C-G

10102776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67426387-G-A

10102776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67426387-G-C

10102776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67426387-G-T

10102849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67426317-A-G

10103460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67426045-C-T

10103546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67425969-C-T

10103640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67425942-A-G

10103654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67425932-C-T

10103757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67425896-C-T

10104060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67425804-C-T

10104164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67425697-C-T

10104174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67425687-C-T

10104382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67425396-T-C

http://identifiers.org/hco/17/GRCh38#10104460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67425296-A-C

10104460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67425296-A-G

10105426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67424092-C-G

10105693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67423830-C-T

10105739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67423784-G-A

10106309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67423216-G-C

10106365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67423154-C-T

10106528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67422987-C-G

10106774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67422715-G-A

10106774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67422715-G-T

http://identifiers.org/hco/17/GRCh38#10106789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67422698-C-A

10106789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67422698-C-T

10111991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67421670-T-A

10112281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67421378-G-A

10112338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67421324-A-T

10112339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67421323-G-C

10112448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67421222-G-T

10113201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67420932-C-G

10114260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67418602-C-T

http://identifiers.org/hco/17/GRCh38#10114335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67418544-C-A

10114335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67418544-C-T

http://identifiers.org/hco/17/GRCh38#10114414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67418471-A-C

10114511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 67418361-C-T

10114703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67418163-C-G

10114896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67417973-T-C

10114901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67417968-T-G

10114993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67417885-C-T

10115020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67417861-T-C

10115175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, undefined
orthologous variants: 67417704-C-T

10115176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, undefined
orthologous variants: 67417703-G-A

10115210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67417669-C-T

http://identifiers.org/hco/17/GRCh38#10115423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#67417435-C-A

10115868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67417037-G-A

10117724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67415540-G-C

10117768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67415494-G-A

http://identifiers.org/hco/17/GRCh38#10117936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67415282-C-A

10117936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67415282-C-T

10117959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67415259-T-A

10118058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67415154-T-G

10118082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67415130-G-C

10118086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67415126-C-G

10118119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67415112-C-T

10118120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67415111-G-A

10118196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67415045-G-A

10119654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67413958-T-C

http://identifiers.org/hco/17/GRCh38#10120131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67413512-A-C

10120131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67413512-A-G

10120133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67413510-C-G

10120273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67413348-G-A

10120459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67413164-G-C

http://identifiers.org/hco/17/GRCh38#10121385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67412403-A-C

10121385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67412403-A-G

10121537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67412258-T-C

10121882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67411953-C-T

10122058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67411763-C-T

10122088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67411726-T-A

10122088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67411726-T-C

http://identifiers.org/hco/17/GRCh38#10122131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67411657-C-A

10122185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67411579-G-A

http://identifiers.org/hco/17/GRCh38#10122233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67411525-C-A

10122293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67411478-T-C

10122385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67411385-T-C

10122394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67411376-T-C

10122418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67411350-C-T

10122634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67411163-T-A

10122640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67411157-C-G

http://identifiers.org/hco/17/GRCh38#10122872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67410967-C-A

http://identifiers.org/hco/17/GRCh38#10122918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67410930-C-A

10123040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67410852-C-G

10123040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67410852-C-T

10123921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67410114-G-C

10124010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67410025-G-C

10124012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67410023-T-C

10124238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67409789-A-G

10124589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67409317-G-A

10124589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67409317-G-T

10124609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67409291-A-G

10125618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67408612-T-G

10125660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67408570-G-A

10125662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67408568-A-G

10125714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67408516-T-G

10125721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67408509-G-A

10125739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67408499-G-A

10125740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67408498-G-A

10125803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67408437-G-A

10125955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67408298-G-A

10125955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67408298-G-C

10125957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67408297-C-G

10126770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67407805-G-A

10126805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67407771-T-C

10127019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67407525-G-A

10127287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67407189-G-C

10127647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67406845-T-C

10127656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67406836-A-T

10127671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67406821-G-A

10127860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67406629-G-C

10128263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67406242-C-T

10128393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67406116-G-A

http://identifiers.org/hco/17/GRCh38#10128499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67405993-C-A

http://identifiers.org/hco/17/GRCh38#10128576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67405916-C-A

10132822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67403038-G-A

10132852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67403008-A-G

http://identifiers.org/hco/17/GRCh38#10135415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67401686-C-A

10135565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67401535-A-G

10135820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67401317-T-C

10135820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67401317-T-G

10135836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67401301-T-C

10136036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67400701-G-A

10136671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67400172-T-C

10136730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67400113-A-G

10139003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67399111-T-A

10139438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67398683-C-T

10140500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67397698-T-C

10140606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67397637-G-A

10140613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67397630-T-C

10140613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67397630-T-G

10140711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67397545-T-G

http://identifiers.org/hco/17/GRCh38#10141459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67396853-A-C

10141459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67396853-A-T

10141528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67396781-A-T

10141544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67396768-C-G

10141766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67396520-A-G

10143668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67394359-G-A

http://identifiers.org/hco/17/GRCh38#10143684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67394343-A-C

10143696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67394331-A-G

10144108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67393963-T-A

10144475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67393638-T-A

10144475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67393638-T-C

10144480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67393633-A-G

10145511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67392563-C-T

10145710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67392375-G-C

http://identifiers.org/hco/17/GRCh38#10145749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67392336-A-C

http://identifiers.org/hco/17/GRCh38#10145755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67392330-C-A

10146524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67391591-T-C

10146525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67391590-T-C

10146972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67389253-T-A

10147045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67389194-T-C

10147045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67389194-T-G

10147156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67389100-A-T

10147336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67388954-G-T

10147589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67388709-G-A

10147594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67388704-T-C

10147627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67388672-G-A

10147648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67388643-T-C

10155413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67388388-T-C

10155636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67388173-G-A

10155654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67388151-T-C

10155661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67388144-A-G

10155712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67388099-T-A

10155752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67388067-C-G

10155757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67388062-G-A

10155860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67387973-A-T

10155899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67387934-A-T

10156133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67387255-C-T

10156163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67387229-G-T

10156228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67387185-G-C

10156308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67387115-C-T

10157193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67385880-C-T

10157196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67385877-G-A

10157196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67385877-G-C

http://identifiers.org/hco/17/GRCh38#10157367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67385710-C-A

10157534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67385563-G-A

10157561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67385534-C-T

http://identifiers.org/hco/17/GRCh38#10160983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67381679-A-C

10161274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67381440-A-G

10161374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67381354-T-G

10161728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67381030-T-C

10161746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67381016-T-C

10161778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67380982-T-C

10162308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67380788-A-T

10162461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67380651-G-A

10162872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67380110-G-A

10162872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67380110-G-C

10162908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67380074-C-T

10162948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67380035-G-A

10163001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67379978-T-C

10163619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67379547-A-G

10163717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67379472-C-T

10163933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67379299-C-T

10164040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67379203-C-T

10164069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67379174-A-G

10165564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67378829-T-C

10165734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67378467-G-C

10168533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67377444-G-A

10168639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67377339-G-A

10169349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67377027-C-G

10169828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67375026-A-G

10169889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67374958-C-G

10169952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67374905-T-C

10170093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67374753-G-A

http://identifiers.org/hco/17/GRCh38#10170153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67374691-C-A

http://identifiers.org/hco/17/GRCh38#10170157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67374687-C-A

10170157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67374687-C-G

10170157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67374687-C-T

10170734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67373961-T-G

10170742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67373945-A-G

10170742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67373945-A-T

10171025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67373591-A-G

http://identifiers.org/hco/17/GRCh38#10171656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67372752-C-A

10171656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67372752-C-T

http://identifiers.org/hco/17/GRCh38#10171719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67372690-A-C

10171719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67372690-A-G

http://identifiers.org/hco/17/GRCh38#10171763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67372650-C-A

http://identifiers.org/hco/17/GRCh38#10171893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67372520-C-A

10172078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67372018-A-G

10172277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67371834-C-T

10172625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67371565-G-A

http://identifiers.org/hco/17/GRCh38#10172651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67371540-C-A

10172651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67371540-C-T

10172731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67371458-T-C

10172746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67371445-G-A

10172771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67371424-C-T

10173007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67371229-A-G

10173021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67371215-C-T

10173619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67370793-T-A

10173624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67370788-C-T

10173637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67370776-G-A

10173730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67370722-T-C

10173847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67370625-G-C

10173847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67370625-G-T

10173877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67370596-C-T

http://identifiers.org/hco/17/GRCh38#10173878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67370595-A-C

10173960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67370516-C-G

10174077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67370461-G-A

10174097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67370443-G-A

10174289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67370278-T-C

10174379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67370193-G-A

http://identifiers.org/hco/17/GRCh38#10176049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67369191-A-C

10176101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67369138-T-C

10176650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67368586-A-G

10176745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67368359-T-A

http://identifiers.org/hco/17/GRCh38#10176972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67368091-A-C

10177215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67367873-G-C

10177244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67367180-A-G

10177251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67367173-G-C

10177491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67366928-G-A

10177491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67366928-G-T

10177783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67366661-T-C

10178539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67365660-C-T

10178552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67365647-A-G

10178552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67365647-A-T

10178603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67365596-C-G

10178606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67365593-A-G

10178685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67365572-C-G

10178799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67365494-C-T

10179061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67365202-G-A

http://identifiers.org/hco/17/GRCh38#10179328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67364959-C-A

10179400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67364882-C-G

10179544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67364745-A-G

10179544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67364745-A-T

10179973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67364434-T-G

10180102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67364312-A-G

10180481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67363966-C-T

10180690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67363733-C-G

10180791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67363614-A-G

10181025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67363417-T-A

10181025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67363417-T-C

10181025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67363417-T-G

http://identifiers.org/hco/17/GRCh38#10181496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67359490-A-C

10183098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67358590-A-G

10183232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67358454-C-T

10183234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67358452-G-A

10183234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67358452-G-C

10183269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67358419-C-T

10183319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67358373-T-A

10183480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67358228-A-G

10183901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67358113-G-A

10184105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67357933-G-A

10184185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67357855-C-T

http://identifiers.org/hco/17/GRCh38#10184203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67357830-A-C

10184375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67357647-T-G

10184408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67357614-C-G

10184408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67357614-C-T

10187484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67355240-G-A

10187746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67354972-C-T

10190567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67353375-A-G

10190622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67353320-G-C

10190649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67353296-T-A

10190649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67353296-T-C

10191877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67353213-A-G

10191895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67353188-G-A

10192190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67352823-C-G

10192190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67352823-C-T

http://identifiers.org/hco/17/GRCh38#10192195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67352818-C-A

10192410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67352588-T-G

10192431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67352570-A-G

10192491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67352517-C-T

10192546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67352470-T-C

10192617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67352399-C-T

10192712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67352305-A-G

10193401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67351683-T-C

10193536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67351550-T-C

10193770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67351162-C-T

10194283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67350418-C-T

10194295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67350407-G-A

10194632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67350099-T-A

http://identifiers.org/hco/17/GRCh38#10194640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67350092-C-A

10195493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67349141-G-A

10195638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67349027-G-A

10195742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67348941-G-A

10195924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67348787-A-G

10196049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67348653-G-A

10196514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67348087-C-G

10196785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67347852-G-A

10196835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67347808-C-T

10196970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67347689-G-C

10197634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67347035-T-A

10197634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67347035-T-G

10197804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67346880-C-T

10197982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: intron variant
orthologous variants: 67346706-G-T

10198344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: missense variant
orthologous variants: 67346462-C-T

10198519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5 prime UTR variant
orthologous variants: 67346287-G-C

10198519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5 prime UTR variant
orthologous variants: 67346287-G-T

10198549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5 prime UTR variant
orthologous variants: 67346257-G-A

10198549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5 prime UTR variant
orthologous variants: 67346257-G-T

10198587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4169
most severe consequence: 5 prime UTR variant
orthologous variants: 67346192-T-C