41631835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79382530-T-C

41631839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79382526-C-T

41631877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79382487-G-C

41631939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79382423-T-C

41632067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79382314-G-A

41632095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79382302-A-G

41632185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79382213-C-T

41632238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79382162-T-C

41632626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79381800-T-C

41632706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79381728-C-T

41638212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79379456-C-T

41638236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79379444-A-G

41638596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79379137-T-C

41639197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79378667-A-T

41639337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79378534-T-A

41639337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79378534-T-C

41640109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79378067-G-A

41640161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79378014-A-G

41640339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79377855-C-T

41640710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79377498-T-C

41640731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79377469-C-T

http://identifiers.org/hco/13/GRCh38#41643870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79375780-A-C

41644100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79375561-C-G

http://identifiers.org/hco/13/GRCh38#41644192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79375522-A-C

41644306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79375442-G-A

41645032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79375297-C-T

http://identifiers.org/hco/13/GRCh38#41645083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79375248-C-A

41645083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79375248-C-T

41645285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79375062-T-G

http://identifiers.org/hco/13/GRCh38#41645554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79374825-C-A

41645605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79374774-G-A

41645743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79374625-T-C

41645748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79374610-C-G

41645832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79374529-T-C

41646422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79374222-T-C

41646422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79374222-T-G

41646431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79374213-T-C

41646467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79374179-G-A

41646502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79374145-T-C

41646747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79373932-T-A

41646747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79373932-T-C

41646800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79373883-A-G

41647030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79373706-G-A

41647065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79373687-G-A

41647351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79373427-T-G

http://identifiers.org/hco/13/GRCh38#41647420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79373365-A-C

41647549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79373254-G-C

41648105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79373091-G-C

41648118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79373078-C-G

41648151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79373045-C-T

41648796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79372433-C-T

http://identifiers.org/hco/13/GRCh38#41649608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79366254-C-A

41649689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79366164-T-A

41649826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79366040-C-T

41650489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79365844-A-G

41650640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79365724-T-C

41650659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79365705-G-A

41650699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79365642-G-A

41650855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79365511-G-A

41650877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79365489-G-A

41650877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79365489-G-C

41650919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79365473-G-A

41650952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79365441-A-T

41650981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79365413-A-T

41651572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79365047-G-C

41651966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79364467-A-G

41652952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79362176-C-T

41653026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79362112-T-A

41653144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79362009-C-T

41653197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79361956-T-C

http://identifiers.org/hco/13/GRCh38#41655489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79360860-C-A

41655489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79360860-C-G

41655546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79360794-T-C

41655619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79360725-G-A

41655635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79360709-C-T

41655751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79360605-G-A

41655777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79360579-G-A

41655822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79360526-G-A

41656204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79360246-G-A

41657216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79359636-T-C

41657316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79359539-T-G

41657503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79359435-A-G

41657510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79359428-T-G

41657633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79359331-G-A

41657674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79359284-A-G

41657954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79359048-G-T

41658785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79356141-G-C

41658858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79356075-A-G

41659522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79354847-T-C

41659531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79354832-T-C

41659566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79354800-C-G

41659566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79354800-C-T

http://identifiers.org/hco/13/GRCh38#41659609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79354756-C-A

41659869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79354519-T-C

41659881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79354510-G-C

41661331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79353783-G-A

41664648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79349915-G-A

41664660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79349903-C-T

41664761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79349829-G-C

41664916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79349670-G-A

http://identifiers.org/hco/13/GRCh38#41665813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79348826-C-A

41666010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79348452-C-G

41666140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79348338-T-C

41666494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79347510-G-A

41666545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79347455-T-C

41666804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79347177-T-C

41666845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79347150-T-C

41666897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79347102-G-A

41667343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79345474-T-C

41667607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79345227-C-G

41667607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79345227-C-T

41667754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79345080-A-T

41667889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79344961-T-C

41667929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79344922-T-C

41668165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79344717-C-T

41668240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, undefined
orthologous variants: 79344648-G-A

41668303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79344571-C-T

41668734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79344172-G-A

41668863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79344037-G-A

41669717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79342364-C-T

41669760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79342321-A-T

41669941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79342146-A-G

41670100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79341951-G-A

41670355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79341655-T-C

41670609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79341425-T-C

41670651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79341394-A-G

41670714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79341336-T-C

41670778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79341278-G-C

41670805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79341256-T-C

http://identifiers.org/hco/13/GRCh38#41670861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79341201-C-A

41670861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79341201-C-T

41670878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79341184-G-C

41670878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79341184-G-T

http://identifiers.org/hco/13/GRCh38#41670919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79341143-A-C

41671058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79341019-A-G

41673964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79340305-G-C

http://identifiers.org/hco/13/GRCh38#41674106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79340154-A-C

41674136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79340130-A-G

http://identifiers.org/hco/13/GRCh38#41675309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79339661-C-A

41675310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79339660-A-G

41675312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79339658-G-T

41675365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79339608-G-T

41678120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79339043-G-A

41678349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79338793-C-T

41678397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79338752-T-C

41678400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79338749-A-G

41678400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79338749-A-T

41678620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79338464-G-A

41679120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79338012-A-G

41679306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79337830-C-T

41683800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79337442-G-A

41683842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79337400-G-A

41684096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79337147-C-T

41684121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79337052-A-G

41684323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79336452-A-G

41684722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79336162-T-C

41684916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79335986-T-A

41684916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79335986-T-C

http://identifiers.org/hco/13/GRCh38#41684924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79335978-A-C

http://identifiers.org/hco/13/GRCh38#41684942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79335963-A-C

41684942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79335963-A-T

41685042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79335872-C-T

41685080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79335834-C-G

41685136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79335778-T-G

http://identifiers.org/hco/13/GRCh38#41685202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79335712-A-C

41685207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: synonymous variant
orthologous variants: 79335707-T-C

http://identifiers.org/hco/13/GRCh38#41685284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79335604-C-A

41685284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79335604-C-T

http://identifiers.org/hco/13/GRCh38#41685291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79335597-C-A

41685291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79335597-C-T

41685329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79335557-T-A

41685330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79335556-A-G

41685330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79335556-A-T

41687456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79335428-T-C

41687516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79335368-G-A

41687636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79335287-A-T

41688056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79334891-C-T

41688086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79334862-T-C

41688100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79334845-G-T

41688155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79334783-C-T

41688181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79334758-T-C

41688210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79334727-T-C

41688247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79334688-C-T

41689046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79334271-A-G

41689244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79334092-T-A

41689248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79334088-T-C

http://identifiers.org/hco/13/GRCh38#41689251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79334085-C-A

41689267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79334071-T-A

41689271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79334067-T-C

41689385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79333946-G-A

41689388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79333943-T-C

41689424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79333907-G-A

http://identifiers.org/hco/13/GRCh38#41689439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79333892-A-C

41689573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79333743-G-T

http://identifiers.org/hco/13/GRCh38#41689641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79333684-C-A

41689850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79333550-G-C

41690080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79333303-T-A

41690080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79333303-T-G

41690156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79333229-T-C

41690156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79333229-T-G

http://identifiers.org/hco/13/GRCh38#41690174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79333211-A-C

41690297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79333088-A-G

http://identifiers.org/hco/13/GRCh38#41690299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79333086-C-A

41690299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79333086-C-T

41690328-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79333038-T-A

41690425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79332947-A-G

41690746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79332412-C-T

41690888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79332167-C-G

41690894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79332161-C-T

41690940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79332118-T-A

http://identifiers.org/hco/13/GRCh38#41690941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79332117-C-A

41690976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79332087-G-C

41690976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79332087-G-T

41691102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331963-A-G

41691124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331941-T-C

41691170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331888-T-C

41691226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331845-A-G

http://identifiers.org/hco/13/GRCh38#41691227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79331844-C-A

http://identifiers.org/hco/13/GRCh38#41691230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79331841-A-C

41691230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331841-A-G

41691236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331835-G-T

41691353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79331728-T-G

41691521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331571-G-C

41691521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331571-G-T

http://identifiers.org/hco/13/GRCh38#41691533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79331559-A-C

41691593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331498-A-G

http://identifiers.org/hco/13/GRCh38#41691594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79331497-C-A

41691594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331497-C-G

41691597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331494-A-T

41691642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331450-A-G

41691674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331422-G-A

41691674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331422-G-T

41691726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331373-A-T

41691729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331370-T-C

41691733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331366-G-A

41691733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331366-G-T

41691827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331276-G-A

41691883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79331219-T-C

41692005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331113-A-G

41692005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331113-A-T

41692048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331091-G-T

41692082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331062-T-C

41692126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331018-A-G

41692324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79330511-C-T

41692339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79330496-T-C

41692524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79330147-C-T

41692614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79330080-T-A

41692688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79330011-T-C

http://identifiers.org/hco/13/GRCh38#41692744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79329961-A-C

41692744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79329961-A-T

41692753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79329952-T-A

41692753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79329952-T-C

41692767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79329938-A-T

41693063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79329641-G-A

41693063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79329641-G-C

41693063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79329641-G-T

41693638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79328970-G-A

41694499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79328049-C-T

41694766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79327490-G-A

41695753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79326368-T-C

41696010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79326099-G-A

41697903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79325570-C-G

41698093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79325363-C-T

41698199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79325152-T-C

41698374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79324916-T-C

41698498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79324789-T-G

41699097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79324231-C-T

41699255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79324073-G-A

41699294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79324032-T-C

41699294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79324032-T-G

41699378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79323955-A-G

http://identifiers.org/hco/13/GRCh38#41699673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79323674-A-C

41699725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79323623-T-C

http://identifiers.org/hco/13/GRCh38#41700328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79322529-C-A

41700525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79321541-G-A

http://identifiers.org/hco/13/GRCh38#41700621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79321451-C-A

41700621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79321451-C-T

41700628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79321444-G-A

41700725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79320978-T-G

41701014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79320701-C-T

41701072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79320676-G-A

41701317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79320424-T-A

41701317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79320424-T-C

41701359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79320383-G-A

41701359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79320383-G-T

41701518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79320223-T-A

41701518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79320223-T-C

41701543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79320198-A-T

41701571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79320171-T-A

41701571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79320171-T-C

41701622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79320140-T-C

41701651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79320116-T-A

41701661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79320106-T-A

http://identifiers.org/hco/13/GRCh38#41701774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79319996-A-C

41701896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79319874-A-G

41701943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79319827-T-G

41701971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79319800-C-T

41702106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79319737-T-A

41702106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79319737-T-G

41702316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79319543-G-A

41702514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79319396-T-C

41702674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79319266-A-G

41702831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79319110-A-G

41702934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79319037-A-G

41703120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79318852-T-C

41703136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79318836-C-T

http://identifiers.org/hco/13/GRCh38#41703190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79318772-C-A

41703228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79318731-T-C

41703228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79318731-T-G

41703243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79318716-G-A

41703243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79318716-G-T

41703293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79318669-T-G

41703364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79318598-T-C

41703364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79318598-T-G

41703475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79318485-A-G

41703534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79318445-T-A

41703534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79318445-T-C

41703534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79318445-T-G

41703549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79318429-T-A

41703549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79318429-T-C

41703549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79318429-T-G

41704130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79317778-T-C

41704254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79317682-A-G

41704274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79317660-C-T

41704324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79317615-C-T

41704335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79317603-T-G

41704670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79317238-T-C

41704728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79317161-G-A

41704728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79317161-G-C

41705200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79316596-T-C

41705320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79316315-G-C

41705345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79316288-G-C

41705448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79315972-A-G

http://identifiers.org/hco/13/GRCh38#41705790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79315709-A-C

41705790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79315709-A-G

http://identifiers.org/hco/13/GRCh38#41706047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79315389-C-A

41706047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79315389-C-T

41706070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79315361-T-C

41706183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79315261-T-C

41706183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79315261-T-G

41706389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79315050-A-G

41706437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79314986-C-T

41706473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79314965-G-C

41706949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79314496-T-C

41707079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79314366-T-G

41707081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79314364-A-G

41707165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79314310-T-C

41707268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79314208-T-A

41707349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79314127-C-G

41707649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79313863-G-C

41707789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79313722-T-C

41707809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79313702-G-A

41707831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79313603-G-A

http://identifiers.org/hco/13/GRCh38#41707868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79313511-C-A

41707889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79313498-T-C

41707965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79313431-T-C

41708028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79313367-A-G

41708133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79313233-G-A

41708152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79313219-G-C

41708156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79313215-G-A

41708160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79313211-C-G

41708160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79313211-C-T

41708186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79313185-C-T

41708557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79312656-G-A

41708697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79312527-G-A

41708894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79312342-T-C

41708993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79312232-T-A

41709287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79311965-T-G

41709380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79311878-C-T

41709864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79311449-C-T

41710066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79311264-G-A

41710366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79310997-G-T

41710490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79310873-T-C

http://identifiers.org/hco/13/GRCh38#41710491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79310872-A-C

41710508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79310855-A-G

41712692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79309392-A-T

41712718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79309366-G-T

41712784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79309296-A-G

41713062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79308999-G-A

41713371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79308731-C-G

http://identifiers.org/hco/13/GRCh38#41713563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79308547-A-C

41713563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79308547-A-G

41713595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79308516-G-T

http://identifiers.org/hco/13/GRCh38#41714045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79308067-A-C

41714045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79308067-A-G

41714182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79307907-T-C

http://identifiers.org/hco/13/GRCh38#41714256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79307841-C-A

41714256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79307841-C-T

41714425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79307698-T-A

41714425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79307698-T-C

41714524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79307635-T-G

41714612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79307595-T-C

http://identifiers.org/hco/13/GRCh38#41714767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79307513-C-A

41714767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79307513-C-T

http://identifiers.org/hco/13/GRCh38#41715040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79307295-C-A

41715040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79307295-C-G

http://identifiers.org/hco/13/GRCh38#41715163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79307175-A-C

41715183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79307155-T-C

41715403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79306975-T-A

http://identifiers.org/hco/13/GRCh38#41715661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79306741-A-C

41716087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79306350-T-C

http://identifiers.org/hco/13/GRCh38#41716090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79306347-C-A

41716153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79306293-A-T

41716171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79306276-A-T

41716217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79306230-G-A

41716238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79306197-A-G

41716261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79306180-C-T

41716269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79306172-A-G

41716319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79306125-C-T

http://identifiers.org/hco/13/GRCh38#41716490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79305844-A-C

41716602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79305753-G-A

41716709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79305646-T-C

41717507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79304120-T-A

41717966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79303801-T-C

41718083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79303679-T-A

41718258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79303516-G-A

41718425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79303387-T-C

41718549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79303274-T-G

41718680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79303158-A-G

41718817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79303078-G-A

41719260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79302782-C-T

41719445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79302596-G-T

41719730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79302304-C-T

41719811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79302224-T-C

http://identifiers.org/hco/13/GRCh38#41719825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79302210-A-C

41719825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79302210-A-G

41719834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79302201-T-C

41719849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79302186-A-T

http://identifiers.org/hco/13/GRCh38#41720451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79301014-A-C

41720515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79300912-T-C

41720625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79300805-T-C

41720628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79300802-A-T

41720635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79300795-A-G

41720733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79300715-G-A

41720733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79300715-G-C

41720870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79300597-G-C

41720902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79300566-T-G

41720910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79300558-C-G

41720924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79300541-T-C

41720973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79300503-C-T

http://identifiers.org/hco/13/GRCh38#41721156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79300306-A-C

41721284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79300182-A-G

41721377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79300120-T-C

41721480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79300017-G-C

41721510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79299987-G-C

41721597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79299899-C-T

41721606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79299890-T-C

41722485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79299540-G-A

41722631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79299373-T-C

41722651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79299353-C-G

41726672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79298257-C-T

41727095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79298173-G-A

41727095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79298173-G-T

41727148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79298120-T-A

41727170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79298110-T-C

41727170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79298110-T-G

41727244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79298036-G-C

41727244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79298036-G-T

41727248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79298032-G-C

41727248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79298032-G-T

41727268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79298012-G-A

41727268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79298012-G-C

41727268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79298012-G-T

41727271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79298009-T-A

41727271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79298009-T-C

41727275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79298005-T-A

41727275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79298005-T-C

http://identifiers.org/hco/13/GRCh38#41727276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79298004-C-A

41727276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: synonymous variant
orthologous variants: 79298004-C-T

41727279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: synonymous variant
orthologous variants: 79298001-T-C

41727282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: synonymous variant
orthologous variants: 79297998-A-G

41727282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: synonymous variant
orthologous variants: 79297998-A-T

41727315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: splice acceptor variant
orthologous variants: 79297965-T-A

41727315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: splice acceptor variant
orthologous variants: 79297965-T-C

41727323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79297957-A-G

41727323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79297957-A-T

41727335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79297949-T-C

41728733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79297507-G-C

41729056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79296835-G-T

41729155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79296740-C-T

41729278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79296481-G-A

http://identifiers.org/hco/13/GRCh38#41729519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79296267-A-C

41729595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79296193-G-A

http://identifiers.org/hco/13/GRCh38#41729703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79296084-A-C

41729735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79296050-T-C

41729754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79296031-G-T

41729764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79296021-A-G

41730209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79295707-T-G

41732084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79294156-G-A

41732096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79294144-T-A

41732096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79294144-T-C

41732112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79294128-C-T

41732307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79293948-T-C

41732312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79293943-G-T

http://identifiers.org/hco/13/GRCh38#41732319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79293936-A-C

41732491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79293791-T-C

41732794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79293545-C-T

41732827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79293514-C-T

41733138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79293201-T-C

41734493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79293006-C-T

41734494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79293005-A-T

41734952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79292616-A-G

41734998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79292571-A-G

41735301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79292275-A-G

41735572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79291946-G-A

41735794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79291545-T-C

41736245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79291102-G-A

41736245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79291102-G-C

41736392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79290955-T-G

http://identifiers.org/hco/13/GRCh38#41736418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79290929-A-C

41736509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79290727-A-G

http://identifiers.org/hco/13/GRCh38#41736675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79290576-A-C

41736704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79290542-C-T

41736772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79290494-C-T

41736776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79290490-A-G

41737561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79288690-T-C

41738102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79288452-G-T

41738272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79288295-C-T

41738526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79287937-A-G

41738619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79287850-T-A

41738623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79287846-A-G

41738703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79287772-A-G

41739038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79287559-T-C

41740729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79286656-T-C

41742246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79286158-G-A

41742260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79286144-T-A

41742316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79286093-C-G

41742316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79286093-C-T

41742338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79286074-C-T

41742409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79286007-G-A

41742545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79285873-A-G

41742824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79285657-A-G

41742909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79285583-T-C

41743253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79285434-T-C

41743404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79285293-G-A

41743495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79285245-T-C

41743663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79285097-C-T

http://identifiers.org/hco/13/GRCh38#41744303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79284788-C-A

41744526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79284402-T-C

41744660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79284293-G-A

41744660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79284293-G-C

41746216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79282483-A-G

41746311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79282421-T-G

41746360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79282373-A-T

41746391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79282338-C-T

http://identifiers.org/hco/13/GRCh38#41746400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79282329-C-A

41746400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79282329-C-T

41746648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79282116-C-T

41746743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79282014-A-T

41751212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79281175-A-T

41751465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79280924-C-G

41751862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79280559-G-A

41751958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79280462-T-C

41751995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79280433-T-A

41751995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79280433-T-C

41752219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79280209-C-T

http://identifiers.org/hco/13/GRCh38#41753457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79279862-A-C

41753518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79279796-T-C

41753633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79279681-G-A

41753744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79279577-G-A

41753890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79279428-T-G

41753955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79279366-A-G

41755401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79278966-C-T

41755530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79278850-T-C

41755592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79278788-A-T

41755767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79278621-G-A

41755767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79278621-G-T

http://identifiers.org/hco/13/GRCh38#41755909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79278494-A-C

41759245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79277697-G-T

41759315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79277625-C-G

41759315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79277625-C-T

41759444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79277484-T-C

41759510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79277418-C-G

41760233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79276717-G-T

41760615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79276314-A-G

41760616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79276313-T-C

41760726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79276199-C-T

41760990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79275775-G-A

41760990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79275775-G-T

41760993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79275772-G-T

41760996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79275769-A-G

41761032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79275733-A-G

41761212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79275555-T-C

41761351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79275449-A-G

41761862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79274963-C-T

http://identifiers.org/hco/13/GRCh38#41762318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79274791-A-C

41763480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79274474-C-T

41763559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79274396-C-G

41763583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79274373-G-A

41763649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79274309-T-C

41763655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79274303-T-A

41763777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79274184-G-A

41763779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79274182-G-A

41764565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79272820-G-A

41764650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79272742-A-G

41764653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79272739-A-G

41764706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79272689-T-C

41764714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79272681-G-A

41764745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79272651-T-G

41764851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79272561-G-A

41764854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79272558-G-C

41765110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79272322-T-A

41765155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79272265-G-A

41765366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79272059-T-C

41765366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79272059-T-G

41765368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79272057-C-T

41765650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79271775-C-T

41765652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79271773-G-A

41765652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79271773-G-C

41765703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79271719-G-T

41765830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79271603-T-C

41766154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79271332-G-A

41766330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79271193-A-T

41766342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79271181-A-G

41766432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79271099-T-C

41766754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79270835-T-C

41766955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79270175-G-C

41767108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79270047-T-C

41767200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79269955-T-C

41767297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79269857-C-T

41767403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79269676-T-C

41767429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79269651-T-C

41767506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79269581-A-G

41767778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79269388-A-G

41767804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79269362-T-C

41767806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79269360-T-C

41768027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79269152-C-T

41768398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79268788-T-A

http://identifiers.org/hco/13/GRCh38#41768481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79268710-A-C

41768481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79268710-A-G

http://identifiers.org/hco/13/GRCh38#41768719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79268510-A-C

41768770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79268463-T-C

41772387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79265955-T-A

41772583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79265800-C-G

41772688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79265705-A-T

http://identifiers.org/hco/13/GRCh38#41772833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79265540-A-C

41772848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79265522-G-A

41772954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79265416-G-C

41773009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79265369-C-G

41773028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79265351-C-G

http://identifiers.org/hco/13/GRCh38#41773040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79265339-C-A

41773253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79265067-T-A

41773590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79264812-G-A

41773590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79264812-G-C

41773831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79264602-T-C

41774510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79264294-C-T

41774549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79264254-A-G

41777866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79263635-T-C

41777896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79263602-A-G

41777923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79263565-T-C

41778089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79263394-T-C

41778096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79263387-T-A

41778096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79263387-T-C

41778316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79263051-C-T

http://identifiers.org/hco/13/GRCh38#41778428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79262876-C-A

41778428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79262876-C-T

41778460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79262824-C-T

http://identifiers.org/hco/13/GRCh38#41778619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79262668-A-C

41779367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79262342-T-A

41779380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79262329-G-C

41779916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79261647-C-T

41780351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79261095-C-G

41780425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79261025-T-A

41780526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79260918-C-G

41780574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79260875-C-G

41780625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79260820-T-C

41780992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79260469-T-A

41781056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79260407-C-T

http://identifiers.org/hco/13/GRCh38#41781060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79260403-A-C

41781091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, undefined
orthologous variants: 79260376-T-C

41781546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79259932-T-G

http://identifiers.org/hco/13/GRCh38#41781584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79259883-A-C

41781689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79259788-C-T

41781697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79259780-G-T

41781879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79259629-T-C

41781879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79259629-T-G

41782260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79259264-T-C

41782473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79259048-G-C

41782824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79258721-T-A

41782969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79258545-A-G

41783100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79258417-A-G

41783690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79258225-A-T

41783733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79258182-G-T

41783777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79258142-A-G

41783845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79258074-C-T

41783889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79258030-G-A

41783897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: synonymous variant
orthologous variants: 79258022-T-C

41783959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79257950-G-A

41783959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79257950-G-C

41783959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79257950-G-T

41783996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79257913-T-C

41784042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79257873-T-C

41785947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79257692-C-T

41786050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79257620-G-A

41786205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79257475-C-T

41786280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79257421-A-G

41786364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79257327-T-C

41786369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79257322-A-G

41786373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79257318-G-A

41786436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79257257-A-G

41786444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79257249-G-A

41786827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79256880-T-C

41786975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79256750-G-C

41787108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79256624-T-C

http://identifiers.org/hco/13/GRCh38#41787331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79256246-C-A

41787331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79256246-C-T

41787517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79256071-G-A

41787663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79255948-G-A

41788285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79254915-A-T

41788556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79254638-C-G

41788763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79254471-T-A

41788790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79254444-T-A

41789934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79254007-A-G

41790093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79253890-A-G

41790216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79253781-A-G

41790300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79253720-A-G

41790535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79253359-A-G

http://identifiers.org/hco/13/GRCh38#41790573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79253321-A-C

http://identifiers.org/hco/13/GRCh38#41790982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79253023-A-C

41791125-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79252894-A-T

41792117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79252165-T-G

41792146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79252138-G-C

41792477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79251837-T-C

41792531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79251788-T-C

41793088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79251316-T-G

41793175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79251216-A-G

41801689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79247202-T-G

41801788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79247107-T-C

http://identifiers.org/hco/13/GRCh38#41811109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79246834-C-A

41811109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79246834-C-T

41811249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79246693-G-A

41811285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79246657-C-T

41811430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79246512-C-T

41811867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79246102-T-C

41812117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79245814-C-T

41812456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79245220-G-C

41812545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79245137-G-C

41812605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79245101-T-C

41813024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79244715-A-G

41813051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79244694-T-C

41813251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79244547-G-C

41813361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79244428-T-G

41814415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79243284-C-T

41814515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79243186-A-G

41814654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79243062-T-C

41815141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79242698-G-A

41815467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79234354-T-C

41815898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79233959-C-T

41816820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79232482-G-C

41816892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79232440-A-G

41819366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79231858-G-A

41819429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79231794-T-G

41819472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79231762-G-A

41819472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79231762-G-T

41819749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79231531-A-T

41819949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79231343-T-C

41820133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79231137-G-C

http://identifiers.org/hco/13/GRCh38#41820538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79230769-C-A

41820696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79230575-T-G

41820709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79230562-A-G

41820709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79230562-A-T

41820773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79230525-T-C

41820786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79230512-T-A

41820839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79230464-G-A

41820839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79230464-G-T

41821209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79230120-T-C

41821387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79229965-G-T

http://identifiers.org/hco/13/GRCh38#41821629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79229734-C-A

41821661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79229701-C-T

41821782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79229593-T-G

http://identifiers.org/hco/13/GRCh38#41821822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79229477-C-A

http://identifiers.org/hco/13/GRCh38#41822134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79229119-C-A

41822203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79229056-G-T

41822245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79229015-A-G

41822367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79228893-C-T

http://identifiers.org/hco/13/GRCh38#41822476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79228792-C-A

41822487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79228782-G-A

41822670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79228621-T-C

41823189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79228381-A-G

41823215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79228352-G-A

41823215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79228352-G-C

41823229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79228340-G-A

41823382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79228183-T-C

41823396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79228169-A-G

41824095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79227101-T-C

41825415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79227026-A-T

41825551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79226895-A-G

41825604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79226851-A-T

http://identifiers.org/hco/13/GRCh38#41825786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79226711-A-C

41825786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79226711-A-G

41826411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79226179-C-T

41826983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79225991-G-T

41827335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79225717-A-G

41827365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79225687-G-C

http://identifiers.org/hco/13/GRCh38#41828159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#79224969-A-C

41830719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79221563-A-G

41830758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79221528-T-A

41830768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79221518-T-A

41830768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79221518-T-C

41830769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79221517-G-A

41830769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79221517-G-T

41830789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79221498-T-C

41830789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79221498-T-G

41830818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79221462-T-C

41830820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79221460-T-C

41830884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79221407-G-A

41830909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79221382-G-A

41830963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79221347-A-G

41831047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79221268-T-C

41831058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79221257-G-A

41831251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79221132-C-T

41831549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79220875-A-G

http://identifiers.org/hco/13/GRCh38#41832560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79220476-C-A

41832717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79220341-G-A

41832717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79220341-G-C

http://identifiers.org/hco/13/GRCh38#41833019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79220116-A-C

41833259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79219886-G-A

41833259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79219886-G-T

41833395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79219810-G-A

41833395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79219810-G-T

41833499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79219706-T-A

41833499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: synonymous variant
orthologous variants: 79219706-T-C

http://identifiers.org/hco/13/GRCh38#41833518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79219687-C-A

41833518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79219687-C-G

41833518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79219687-C-T

http://identifiers.org/hco/13/GRCh38#41833601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79219598-C-A

41833604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79219595-G-A

41833604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79219595-G-C

41833604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79219595-G-T

41833610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79219589-A-G

41833610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79219589-A-T

http://identifiers.org/hco/13/GRCh38#41833626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79219575-C-A

41833626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79219575-C-G

http://identifiers.org/hco/13/GRCh38#41833865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79219335-A-C

41834212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79218921-T-A

41834212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79218921-T-C

41834408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79218735-T-C

41834516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79218646-T-C

41834528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79218634-T-G

41835384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79217297-T-C

41835652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79215733-A-G

http://identifiers.org/hco/13/GRCh38#41835765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79215661-C-A

41835876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79215565-C-T

http://identifiers.org/hco/13/GRCh38#41836195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79215303-C-A

41836440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79214917-A-G

41837812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79213470-T-C

41837894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79213389-C-T

41837951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79213335-G-A

41838160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79213136-A-G

41838352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79212972-A-G

41838380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79212944-T-A

41838384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79212940-G-A

41838446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79212873-T-C

41838683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79212481-A-T

41841866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79211743-G-A

41841866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79211743-G-T

41841867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79211742-T-A

41841867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79211742-T-G

41841934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79211668-C-T

41842102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79211368-A-G

41842499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79211044-T-A

41842510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79211033-G-A

http://identifiers.org/hco/13/GRCh38#41842735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79210174-C-A

41842760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79210149-A-G

41846461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79209325-A-G

41847123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79208498-T-C

http://identifiers.org/hco/13/GRCh38#41847161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79208460-A-C

41847392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79208263-T-A

41847459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79208192-G-A

http://identifiers.org/hco/13/GRCh38#41847465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79208186-C-A

http://identifiers.org/hco/13/GRCh38#41848025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79207488-A-C

41848114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79207379-T-C

41848337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79207165-T-C

41848819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79207051-G-A

41848914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79206958-C-T

41849003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79206869-T-G

41849052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79206820-T-A

http://identifiers.org/hco/13/GRCh38#41850259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79206095-A-C

41855099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79194784-T-C

41859466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79194443-G-A

41859466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79194443-G-T

41859854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79194064-T-C

41860040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79193857-C-T

41860247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79193633-G-A

41860608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79188738-A-G

41860638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79188716-G-A

41860638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79188716-G-T

http://identifiers.org/hco/13/GRCh38#41860906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79188456-A-C

http://identifiers.org/hco/13/GRCh38#41865492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79187224-C-A

41865568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79187138-G-A

41865568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79187138-G-T

http://identifiers.org/hco/13/GRCh38#41865643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79187092-C-A

http://identifiers.org/hco/13/GRCh38#41865819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79186932-A-C

41865819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79186932-A-G

41866611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79186551-C-T

41868246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79184823-C-T

41868303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79184752-G-A

41868303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79184752-G-T

41868597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79184484-A-G

41868597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79184484-A-T

http://identifiers.org/hco/13/GRCh38#41868998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79184416-C-A

http://identifiers.org/hco/13/GRCh38#41869054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79184364-C-A

41869135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79184272-C-T

41869241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79184182-G-A

41869584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79184088-T-C

41869736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79183975-G-A

41869942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79183800-A-G

http://identifiers.org/hco/13/GRCh38#41870266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79183508-A-C

41874833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79183057-T-C

41874833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79183057-T-G

41874895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79183004-T-C

41877199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79179918-G-A

41877199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79179918-G-T

41878386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79178845-G-C

41878388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79178843-T-A

41878460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79178797-T-A

41878495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79178765-T-C

41878644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79178668-T-C

41879949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79176965-T-A

http://identifiers.org/hco/13/GRCh38#41880367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79176380-C-A

41880367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79176380-C-T

41880406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79176340-C-T

41880555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79176219-C-T

41881090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79175720-T-C

41882982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79175021-C-T

41883278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79174743-T-G

41883350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79174683-G-T

41883544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79174486-A-G

41883558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79174470-G-A

41883558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79174470-G-T

41883565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79174463-T-C

41883569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79174459-A-G

41883570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79174458-T-C

41883660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79174377-C-T

41883779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79174271-C-T

41884089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79173958-T-G

41884587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79173864-A-T

41884796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79173704-T-C

http://identifiers.org/hco/13/GRCh38#41885176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79173401-C-A

41885185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79173393-G-A

41885567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79173051-T-C

41885669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79172963-C-T

41885780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79172859-G-A

41885780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79172859-G-T

41885789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79172853-A-G

41886351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79172306-A-G

41886421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79172272-C-T

41886758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79172099-G-A

41886805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79172057-A-G

41886872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79171993-T-C

41886895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79171970-T-C

41886930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79171944-C-T

41887185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79171279-G-C

41887440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79170992-T-C

41887451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79170981-T-A

41887457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79170975-G-A

41887458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79170974-A-G

41887458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79170974-A-T

http://identifiers.org/hco/13/GRCh38#41887484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79170948-A-C

41887520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79170912-G-C

41887621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79170767-C-T

41887704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79170706-G-A

41888276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79170149-T-C

41888343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79169837-A-G

41888352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79169824-T-C

41888464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79169729-G-T

41888572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79169627-A-G

41888769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79169427-G-C

http://identifiers.org/hco/13/GRCh38#41889026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79169237-C-A

41889752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79167916-C-G

41889752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79167916-C-T

41889985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79164158-C-T

41891046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79163146-C-T

41891284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79162975-G-T

http://identifiers.org/hco/13/GRCh38#41891329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79162926-C-A

41891329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79162926-C-T

41891352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79162922-T-C

41891382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79162901-G-C

41891382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79162901-G-T

http://identifiers.org/hco/13/GRCh38#41891402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79162885-A-C

41891411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79162876-T-G

http://identifiers.org/hco/13/GRCh38#41891517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79162770-A-C

41891592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79162695-T-C

41891613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79162676-A-G

http://identifiers.org/hco/13/GRCh38#41891705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79162606-A-C

41891707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79162604-G-C

41891707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79162604-G-T

41892031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79162290-A-G

41892458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79161962-T-C

41892500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79161920-G-A

41892742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79161689-C-T

41892827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79160914-T-A

41893095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79160698-A-G

41893145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79160669-T-C

41893201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79160607-T-C

41893283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79160542-T-G

http://identifiers.org/hco/13/GRCh38#41893306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79160519-A-C

http://identifiers.org/hco/13/GRCh38#41893438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79160381-C-A

41893438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79160381-C-T

41894071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79160106-C-T

http://identifiers.org/hco/13/GRCh38#41894750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79159651-A-C

41894766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79159635-G-C

41894807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79159558-G-A

http://identifiers.org/hco/13/GRCh38#41894908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79159460-C-A

41894939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79159429-G-A

41899595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79157636-T-G

41899760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79157503-T-C

41899760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79157503-T-G

41900031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79157254-C-T

http://identifiers.org/hco/13/GRCh38#41900337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79156965-A-C

41900484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79156819-A-G

41900689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79156628-G-A

41900708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79156615-A-G

41900822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79156501-G-A

41900823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79156500-C-G

41901999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79154355-A-G

41903298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79153041-T-C

41907141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79150123-T-A

41907141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79150123-T-C

41907143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79150121-C-T

41907220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79150044-C-T

http://identifiers.org/hco/13/GRCh38#41907506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79149794-C-A

41907506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79149794-C-T

41907511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79149789-C-T

41907689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79149614-G-A

41907732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79149571-A-G

http://identifiers.org/hco/13/GRCh38#41907778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79149525-C-A

41907778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79149525-C-T

41907817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79149487-G-T

41907838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79149469-G-A

41907838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79149469-G-C

41907838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79149469-G-T

41908031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79148849-G-C

41908122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79148752-A-G

41908155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79148715-G-A

41908155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79148715-G-C

41909556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79148082-T-C

41910017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79147288-G-A

41910044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79147263-G-A

http://identifiers.org/hco/13/GRCh38#41910214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79147086-A-C

http://identifiers.org/hco/13/GRCh38#41911037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79146410-C-A

41911037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79146410-C-T

41911454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79146313-A-G

41911456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79146311-C-T

41911475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79146270-A-G

41911522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79146225-G-C

41911661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79146073-T-C

http://identifiers.org/hco/13/GRCh38#41911887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79145849-C-A

41911887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79145849-C-T

41911891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79145845-A-T

http://identifiers.org/hco/13/GRCh38#41911971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79145767-A-C

41912012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79145717-G-T

41912106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: synonymous variant
orthologous variants: 79145623-A-G

41912174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79145555-A-G

41912184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79145545-A-G

41912195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79145534-T-C

41912195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79145534-T-G

41912299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79145441-A-G

41912302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79145438-T-C

41912310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79145427-T-C

41912632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79145164-T-G

http://identifiers.org/hco/13/GRCh38#41913518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79142051-C-A

41913518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79142051-C-T

http://identifiers.org/hco/13/GRCh38#41913784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79141749-A-C

41913889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79141703-G-A

http://identifiers.org/hco/13/GRCh38#41913957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79141636-C-A

41915363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79140288-T-C

41915591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79140085-A-G

41915736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79139941-A-T

41915770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79139929-G-C

41915897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79139508-T-C

http://identifiers.org/hco/13/GRCh38#41916011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79139392-A-C

41916693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79138522-T-C

41916909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79138311-G-A

41917379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79137860-C-T

41917539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79137786-T-G

41917629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79137705-A-G

41917768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79137505-A-G

41917832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79137333-T-G

http://identifiers.org/hco/13/GRCh38#41917883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79137295-C-A

41917883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79137295-C-T

41917887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79137291-G-C

41917995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79137205-T-C

41918158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79137037-G-A

41918197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79136997-A-T

41938811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79123764-G-A

41938834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79123744-T-C

http://identifiers.org/hco/13/GRCh38#41938863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79123716-A-C

41938972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79123600-T-C

41939066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79123506-T-C

41939229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79123349-G-A

41939383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79123197-A-G

41939809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79122764-T-C

41939855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79122722-A-T

41939885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79122682-C-G

41939930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79122643-C-G

41940824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79121325-T-A

41940824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79121325-T-C

41941967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79120086-T-C

http://identifiers.org/hco/13/GRCh38#41942022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79120031-C-A

41942539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79119299-T-C

41942721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79119108-G-A

41942844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79118951-G-C

41942940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79118815-T-C

41942973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79118784-G-C

41943054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79118718-C-T

41943061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79118711-T-G

41943070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79118702-T-G

41949845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79106386-A-G

41949896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79106329-T-C

41949977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: missense variant
orthologous variants: 79106253-A-G

41950075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79106152-G-T

41950077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79106150-A-G

http://identifiers.org/hco/13/GRCh38#41950107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79106120-A-C

41950131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79106096-C-G

http://identifiers.org/hco/13/GRCh38#41950268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79105990-A-C

http://identifiers.org/hco/13/GRCh38#41951475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79103012-A-C

http://identifiers.org/hco/13/GRCh38#41951594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79102906-A-C

41951741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79102763-G-A

41951787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79102717-T-A

41951831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79102676-T-C

http://identifiers.org/hco/13/GRCh38#41953054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79099891-A-C

http://identifiers.org/hco/13/GRCh38#41954019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79099421-C-A

41954200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79099266-A-T

41954281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79099219-T-C

41954399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron variant
orthologous variants: 79099108-C-T

41955835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79090364-G-T

41956141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79090100-T-A

41956309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79089964-G-C

41956309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79089964-G-T

41956332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79089942-C-T

41957698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79089169-A-G

41958276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79088508-G-C

41958389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79088395-T-C

41958543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79088255-T-C

41958578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79088220-T-C

41958621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79088177-C-T

41960284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79087282-T-C

41960465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79087137-T-G

41960476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79087126-A-G

41960550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79087052-G-A

41960608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79087000-A-T

41960699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79086910-G-A

41960846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 79086888-G-A

41960846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 79086888-G-T

41960872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 79086865-G-A

41960872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 79086865-G-T

http://identifiers.org/hco/13/GRCh38#41960914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#79086823-C-A

41960914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 79086823-C-T

http://identifiers.org/hco/13/GRCh38#41960926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79086811-C-A

41960926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79086811-C-T

http://identifiers.org/hco/13/GRCh38#41960938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#79086799-C-A

41960938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 79086799-C-G

41960938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 79086799-C-T

41960945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 79086792-A-G

http://identifiers.org/hco/13/GRCh38#41960951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#79086786-A-C

41960951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 79086786-A-G

41960977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 79086760-G-A

41960977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 79086760-G-C

41960977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 79086760-G-T

http://identifiers.org/hco/13/GRCh38#41960981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#79086756-C-A

41960981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 79086756-C-T

41960999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 79086738-A-G

http://identifiers.org/hco/13/GRCh38#41961029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#79086709-C-A

41961029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79086709-C-G

41961029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79086709-C-T

41961030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79086708-T-A

41961030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79086708-T-C

41961030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79086708-T-G

41961091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79086654-G-A

41961091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79086654-G-C

41961091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79086654-G-T

http://identifiers.org/hco/13/GRCh38#41961092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#79086653-C-A

41961092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79086653-C-T