9292897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 5 prime UTR variant
orthologous variants: 150039468-C-T

http://identifiers.org/hco/1/GRCh38#9293097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#150039283-C-A

9293097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150039283-C-T

9293168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150039221-G-A

9293168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150039221-G-C

9293168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150039221-G-T

9293345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150039073-T-G

http://identifiers.org/hco/1/GRCh38#9293355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#150039056-A-C

9293435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150038961-G-T

9293717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150038653-C-T

9293735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150038635-T-C

9293749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150038619-C-T

9294358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150038434-G-A

9294693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150038094-G-T

9294745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150038042-A-G

9294837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150037822-C-T

9295979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150037011-C-G

9296374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150036669-C-T

9296483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150036485-G-A

9296807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150036130-C-T

9296844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150036065-T-C

http://identifiers.org/hco/1/GRCh38#9297042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#150035870-C-A

9308708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150031170-C-T

9309184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150030891-T-C

9309995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150030677-C-T

9310153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150030581-G-A

http://identifiers.org/hco/1/GRCh38#9310159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#150030574-A-C

9310819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150030311-G-A

9310847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150030285-C-G

9310941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150030186-G-A

9310941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150030186-G-T

9310992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150030157-A-G

9311147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150030007-C-T

9311452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150029724-C-G

9311526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150029663-G-A

9314422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150029135-G-T

9314457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150029106-C-G

9314509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150029072-A-G

9314535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150029039-C-T

9314622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150028956-C-G

9314622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150028956-C-T

9314805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150028802-G-T

9314853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150028764-G-T

9314881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150028754-C-T

9315174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150028452-G-A

http://identifiers.org/hco/1/GRCh38#9315188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#150028438-C-A

9315646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150028066-C-T

9315906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150027808-C-T

9315950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150027765-C-T

9316098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150027623-C-T

9316404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150027321-G-A

9316481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150027190-A-G

9316712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150026973-G-A

9316718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150026967-A-G

9316742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150026943-A-G

9316890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150026784-G-A

9317225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150026523-A-T

9317283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150026467-G-A

9317283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150026467-G-C

9317298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150026449-T-C

9318042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150026058-C-T

9318059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150026038-G-A

9318169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150025935-G-T

9318205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150025901-C-G

9318316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150025812-C-G

9318359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150025769-C-T

9318654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150025506-G-A

9318748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150025455-C-G

9318748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150025455-C-T

9318752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150025451-G-A

9320228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150024813-G-A

9320349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150024693-A-G

9320399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150024642-C-G

9320399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150024642-C-T

http://identifiers.org/hco/1/GRCh38#9320716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#150023943-C-A

9320716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150023943-C-T

9320740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150023919-A-G

9320922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150023747-T-C

9320932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150023737-A-G

9321168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150023442-A-T

http://identifiers.org/hco/1/GRCh38#9322063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#150022474-C-A

http://identifiers.org/hco/1/GRCh38#9322229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#150022329-A-C

9322378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150022197-C-T

9322471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150022097-C-T

9322645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150021912-T-C

9322679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150021879-C-T

9322826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150021753-G-C

9322826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150021753-G-T

9322885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150021691-C-T

9322888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150021688-T-C

9323135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150021422-C-T

9323265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150021308-C-T

9323385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150021208-C-G

9323409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150021177-C-T

http://identifiers.org/hco/1/GRCh38#9323429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#150021156-C-A

9324055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150020653-G-A

9324082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150020621-T-C

9324115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150020609-A-G

9324152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150020591-A-G

9324343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150020377-C-G

9324460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150020264-A-G

9324526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150020200-T-A

9324554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150020169-G-T

9324654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150020071-C-G

9324654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150020071-C-T

9324725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150020001-T-G

9324945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150019791-G-A

9325051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150019689-G-C

9325192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150019590-G-A

9325192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150019590-G-T

9325211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150019570-T-G

9325413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150019403-C-T

9325438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150019385-T-C

9325491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150019334-G-A

9325517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150019301-C-T

9325542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150019276-G-A

http://identifiers.org/hco/1/GRCh38#9326227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#150016633-C-A

http://identifiers.org/hco/1/GRCh38#9326420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#150016489-C-A

9326678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150016260-C-T

9326982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150015980-C-T

9327138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150015846-C-T

9327161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150015836-C-G

9327183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150015820-C-T

http://identifiers.org/hco/1/GRCh38#9327189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#150015810-C-A

9327213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150015787-G-T

9327241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150015745-A-G

http://identifiers.org/hco/1/GRCh38#9327358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#150015601-A-C

9327358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150015601-A-G

9327358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150015601-A-T

9327368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150015591-G-T

9327404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150015548-A-G

9327557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150015406-T-C

9332772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150014408-G-A

9332932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150014270-G-A

9332940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150014263-C-T

9334052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150013439-T-C

9336820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150008762-C-T

http://identifiers.org/hco/1/GRCh38#9336825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#150008757-C-A

9336896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150008695-G-A

9337132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150008509-A-G

9337282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150008360-G-A

9337313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150008331-A-G

9337515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150008156-A-G

9337760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150008034-C-T

9338313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150007691-C-G

9338326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150007678-G-A

9338583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150007493-T-A

9338879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150007160-G-T

9339024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150007003-C-T

9339085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150006945-C-T

http://identifiers.org/hco/1/GRCh38#9339105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#150006921-C-A

9339105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150006921-C-T

9339114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150006912-G-T

http://identifiers.org/hco/1/GRCh38#9339183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#150006819-C-A

9339183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150006819-C-G

http://identifiers.org/hco/1/GRCh38#9339376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#150006627-C-A

9339376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150006627-C-T

http://identifiers.org/hco/1/GRCh38#9339513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#150006485-C-A

9339520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150006480-G-C

9339853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150006153-C-T

9340129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150005789-G-A

9340231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150005673-T-G

9340280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150005625-C-T

9340426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150005526-G-T

9340542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150005410-T-C

9340704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150005244-G-A

9340769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150005200-T-C

9340898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150005076-G-A

9340933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150005063-G-A

9341032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150004980-G-A

9341164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150004861-C-G

9341184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150004842-C-T

9341213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150004811-A-G

9341220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150004804-A-G

9342267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150003559-G-A

http://identifiers.org/hco/1/GRCh38#9342343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#150003500-C-A

9342405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150003440-T-C

9342734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150003108-C-T

9342871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150002963-T-C

9342881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150002953-C-T

9342927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150002924-C-T

9342991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 150002863-A-G

9344585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149999975-G-A

9344585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149999975-G-C

9344661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149999892-A-T

9345713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149999023-T-C

9345720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149999016-G-A

9345786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149998950-A-G

9346689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149998094-C-T

9346726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149998062-G-T

9349281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron_variant, undefined
orthologous variants: 149996236-C-T

9349412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149996137-G-T

9349452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149996106-T-C

9349480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149996075-C-T

9349481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149996074-G-A

9349522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149996019-T-A

9349779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149995713-C-T

9349797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149995695-C-G

9349797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149995695-C-T

9349847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149995640-A-G

9350088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149995467-C-T

9350270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149995297-G-A

9350921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149994653-G-A

9351037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149994535-C-T

9351278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149994305-C-T

9351513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 149994050-G-A

9351545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 149994026-C-T

9351561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 149994000-T-C

9351655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149993713-T-C

9351692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149993675-G-A

9352057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149993351-G-A

9352214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149993222-G-A

9352417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149993041-C-G

9352485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149992972-T-C

9355381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149992054-G-A

http://identifiers.org/hco/1/GRCh38#9355501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149991929-C-A

9355531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149991896-G-A

9355559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149991869-G-T

http://identifiers.org/hco/1/GRCh38#9355569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149991858-C-A

9355569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149991858-C-T

9355578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149991847-G-T

9355584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149991841-T-G

http://identifiers.org/hco/1/GRCh38#9355598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149991827-A-C

9355598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149991827-A-G

http://identifiers.org/hco/1/GRCh38#9355601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149991824-C-A

9355601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149991824-C-T

http://identifiers.org/hco/1/GRCh38#9355644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149991817-C-A

9355644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149991817-C-T

9355651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149991810-G-T

9355668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149991793-G-A

9355668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149991793-G-C

9355668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149991793-G-T

9355689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149991771-T-C

9355689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149991771-T-G

9355720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 149991740-T-C

9355734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 149991721-G-A

9355734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 149991721-G-T

9355832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 5 prime UTR variant
orthologous variants: 149991623-G-T

9355907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: missense variant
orthologous variants: 149991549-A-G

9356024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: missense variant
orthologous variants: 149991432-C-T

9356066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: missense variant
orthologous variants: 149991390-A-G

http://identifiers.org/hco/1/GRCh38#9356123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149991333-C-A

http://identifiers.org/hco/1/GRCh38#9356474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149990982-C-A

9356669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149990796-T-C

9356700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149990769-C-T

9356733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149990731-A-G

9356733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149990731-A-T

9356779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149990685-A-G

9357366-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149990511-T-A

http://identifiers.org/hco/1/GRCh38#9357601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149990284-A-C

9357644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149990246-A-G

9357675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149990227-G-A

9357962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149989937-C-T

9357992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149989909-C-T

http://identifiers.org/hco/1/GRCh38#9358440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149989551-C-A

9358511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149989479-G-A

9358629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149989392-C-T

9358684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149989342-C-T

9358866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149989185-A-G

9362730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149986244-T-C

9362800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149986174-C-T

9363557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149985558-A-G

9363632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149985478-C-T

9364179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149985264-G-A

9364197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149985246-C-G

9364197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149985246-C-T

9364256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149985203-C-T

9364322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149985142-C-T

9366962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149983293-G-A

9366962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149983293-G-C

9366962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149983293-G-T

9367071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149983186-G-A

9367228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149983039-G-A

9367228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149983039-G-C

9367319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149982963-T-A

9367319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149982963-T-G

http://identifiers.org/hco/1/GRCh38#9367321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149982961-C-A

9367321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149982961-C-T

9367381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149982872-G-A

9367382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149982871-T-A

9367393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149982860-G-A

9367393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149982860-G-C

9367393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: intron variant
orthologous variants: 149982860-G-T

9367489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: missense variant
orthologous variants: 149982755-C-T

9367533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: synonymous variant
orthologous variants: 149982711-G-C

9367578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149982666-T-G

http://identifiers.org/hco/1/GRCh38#9367647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149982603-C-A

9367668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149982582-G-A

9367668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149982582-G-C

9367668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149982582-G-T

http://identifiers.org/hco/1/GRCh38#9367847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149982434-A-C

9367847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149982434-A-G

9367870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149982415-G-A

9367870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149982415-G-T

9368160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149982173-G-A

http://identifiers.org/hco/1/GRCh38#9368322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149982025-C-A

9368322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149982025-C-T

9368360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149981976-T-C

9368398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149981937-G-A

9368398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149981937-G-C

9368398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149981937-G-T

http://identifiers.org/hco/1/GRCh38#9368466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149981905-C-A

9368466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149981905-C-T

http://identifiers.org/hco/1/GRCh38#9368611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149981787-C-A

9368611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149981787-C-G

9368625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149981773-G-T

9368673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149981727-A-G

9368730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149981674-A-G

9368730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149981674-A-T

9368766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149981639-C-T

9368767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149981638-G-A

9368767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149981638-G-T

9368800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149981623-T-C

9368800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149981623-T-G

9368834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149981607-C-T

http://identifiers.org/hco/1/GRCh38#9368835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149981606-C-A

9368855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149981587-G-T

http://identifiers.org/hco/1/GRCh38#9368900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149981543-C-A

9368920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149981514-A-G

9369135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149981125-A-G

9369186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149981074-C-T

9369283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149980987-T-G

http://identifiers.org/hco/1/GRCh38#9369324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149980959-C-A

9369397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149980884-G-T

http://identifiers.org/hco/1/GRCh38#9369402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149980879-C-A

9369402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149980879-C-T

9369413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30628
most severe consequence: 3 prime UTR variant
orthologous variants: 149980868-C-T