101028749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5 prime UTR variant
orthologous variants: 49059293-T-A

101028749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5 prime UTR variant
orthologous variants: 49059293-T-C

101028893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5 prime UTR variant
orthologous variants: 49059423-A-G

http://identifiers.org/hco/9/GRCh38#101028991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49059506-C-A

101028991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5 prime UTR variant
orthologous variants: 49059506-C-T

101029111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49059626-G-A

101029111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49059626-G-T

101029411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49059924-T-G

101029679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49060177-C-T

101029813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49060313-G-A

101030141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49060631-G-A

101030406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49060876-C-T

101030465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49060934-T-G

101030474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49060942-T-A

101030663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49061104-C-T

101030721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49061159-G-C

101030733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49061166-T-G

101030744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49061177-G-T

http://identifiers.org/hco/9/GRCh38#101030910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49061291-C-A

http://identifiers.org/hco/9/GRCh38#101030929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49061306-C-A

101030929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49061306-C-T

101030938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49061315-G-A

101031026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49061402-A-G

101031028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49061404-T-C

101031219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49061558-T-C

101031728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49062069-G-A

101031857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49062205-A-T

101032122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49062473-A-G

101032845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49063165-A-G

101033160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49063481-A-G

101033759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49064411-C-T

101033871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49064513-C-G

101034060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49064691-C-T

101034137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49064761-G-A

101034251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49064867-G-T

101034958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49066072-C-T

101035015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49066116-A-G

101035367-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49066447-A-T

101035446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49066504-C-T

101036146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49067116-T-G

101036370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49067339-T-C

101036462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49067435-T-C

101036547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49067519-C-T

http://identifiers.org/hco/9/GRCh38#101036660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49067612-C-A

101036692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49067635-T-A

101036692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49067635-T-G

101036749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49067664-G-A

101036780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49067693-G-A

101036981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49067919-T-A

101036981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49067919-T-C

101037037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49067969-A-G

101037041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49067973-C-T

101037103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49068026-A-G

101037502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49068412-C-T

http://identifiers.org/hco/9/GRCh38#101037555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49068465-A-C

101037787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49068691-G-T

101037814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49068722-A-G

101037830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49068739-G-T

101038140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49069050-A-T

101038469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49069312-T-C

101038688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49069539-G-T

101038733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49069587-G-T

101038759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49069613-A-G

101038834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49069684-A-G

101038926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49069763-T-C

101040222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49070547-A-T

101040281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49070605-G-A

http://identifiers.org/hco/9/GRCh38#101040475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49070791-C-A

101040482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49070798-G-T

101040540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49070868-C-G

101040551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49070883-G-C

101040567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49070899-T-C

101040706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49071040-A-G

101040706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49071040-A-T

101041083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49071344-G-T

101041090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49071351-T-C

101046917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49071700-A-G

101047299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49071921-A-G

101047300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49071922-C-T

101047367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49071989-T-C

101047507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49072123-T-C

101047535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49072150-G-A

101047919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49072707-A-G

101047953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49072741-G-T

101048094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49072991-G-A

101048094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49072991-G-C

101048428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49073326-G-A

101048508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49073403-T-C

101048795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49073687-A-G

101048912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49073787-T-C

101049450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49074914-G-A

101049565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49075018-C-T

101049567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49075020-G-C

101049661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49075105-G-A

101050165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49075459-C-G

101050380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49075650-A-T

101050559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49076042-A-G

101051064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49076477-A-G

101051216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49076613-C-T

101051622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49076921-A-G

101051812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49077097-G-A

101051850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49077135-C-T

101051877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49077160-A-G

101052961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49078062-G-T

101053061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49078163-T-G

101053066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49078168-T-C

101053159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49078259-C-T

101053160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49078260-C-T

101053330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49078426-G-T

101053441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49078548-C-T

http://identifiers.org/hco/9/GRCh38#101053492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49078606-C-A

101053559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49078681-G-A

101053740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49078810-G-A

101053771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49078840-C-T

101053774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49078843-G-C

101054277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49079016-C-T

101054549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49079278-A-G

101054561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49079290-G-A

101054568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49079297-C-G

101054639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49079371-G-A

101054686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49079418-C-T

101054701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49079433-A-G

101054722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49079454-A-G

101054892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49079622-G-A

101054912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49079642-G-A

101054933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49079666-G-A

101054988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49079711-T-A

101055268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49079962-C-T

101055492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49080188-T-A

101055903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49080600-T-C

http://identifiers.org/hco/9/GRCh38#101055996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49080689-C-A

101056102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49080793-G-A

101056112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49080803-C-T

101056114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49080805-A-G

101056117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49080808-A-G

101057558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49085934-A-G

101057597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49085974-A-G

101057760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49086708-G-A

101058071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49086968-C-T

101058105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49087002-A-T

101058168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49087213-G-A

http://identifiers.org/hco/9/GRCh38#101058339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49087573-C-A

101058567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49087834-A-G

101059237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49088380-T-C

101059584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49088726-T-A

101059779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49088912-C-G

101060048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49089197-G-C

101060115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49089241-A-G

101060238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49089292-A-T

101060304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49089348-C-T

101060353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49089397-A-G

101060608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49089974-G-C

101061129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49090543-G-A

101063332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49092465-G-A

101063389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49092519-G-A

101063413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49092544-T-C

101063416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49092547-T-C

101063440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49092569-A-G

101064097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49093172-A-G

101064141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49093213-C-G

101064170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49093238-T-C

101064218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49093286-C-T

http://identifiers.org/hco/9/GRCh38#101065725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49095979-A-C

101065777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49096058-T-C

101065843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49096132-G-C

101066048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49096338-G-C

101066085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49096375-C-G

101066152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49096434-G-A

101066192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49096483-T-G

101067592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49096588-G-A

101067716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49096712-C-T

101067763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49096757-C-G

101067909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49096884-A-G

101068077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49097041-T-C

101068127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49097091-T-C

101068357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49097605-G-A

101068600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49097823-T-C

101068661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49097882-C-G

101068716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49097937-C-T

101068889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49098104-A-G

http://identifiers.org/hco/9/GRCh38#101069513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49098695-C-A

http://identifiers.org/hco/9/GRCh38#101069541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49098714-C-A

101069609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49098777-T-C

101069637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49098805-T-C

101069651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49098819-G-A

101069771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49098948-A-G

101069771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49098948-A-T

101069791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49098966-G-T

101072653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49101172-G-A

101072742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49101265-T-A

101073021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49101824-A-G

101073138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49101939-T-C

http://identifiers.org/hco/9/GRCh38#101073144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49101945-C-A

101073273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49102082-A-G

101073293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49102102-T-A

101073647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49102459-C-T

101073769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49102582-A-G

101073976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49102797-G-A

101074050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49102871-T-C

101074114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49102939-A-G

101074500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49103308-A-G

101074566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49103614-T-C

101074723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49103744-G-T

101075055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49104030-A-G

http://identifiers.org/hco/9/GRCh38#101075263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49104260-C-A

101075263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49104260-C-G

101075495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49104491-C-T

101076120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49105026-T-C

101076178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49105065-G-A

101076235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49105119-G-A

101076738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49105615-T-C

101076813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49105694-A-T

101077173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49106295-C-T

101077433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49106499-T-C

101077433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49106499-T-G

101077567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49106609-A-T

101077630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49106661-A-G

101077679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49106709-C-G

101077855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49106868-T-A

101077926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49106940-C-G

101081547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49108321-C-T

101081805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49108595-A-G

101081982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49108772-G-A

101082012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49108796-T-A

101082028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49108811-C-G

http://identifiers.org/hco/9/GRCh38#101082033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49108816-A-C

101082259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49109012-T-G

101082275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49109028-T-C

101082290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49109043-T-C

101082290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49109043-T-G

101082325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49109078-C-T

101082328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49109081-G-A

101082330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49109083-T-C

101082498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49109552-C-T

101082752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49109813-G-A

101082979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49110036-G-A

http://identifiers.org/hco/9/GRCh38#101083074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49110129-A-C

101083077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49110132-G-A

101083170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49110218-T-G

101083220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, undefined
orthologous variants: 49110262-G-A

101083226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, undefined
orthologous variants: 49110268-T-G

101083418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49110618-T-A

101083440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49110643-A-G

101083468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49110670-G-T

101083523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49110725-T-C

101083652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49110853-G-A

101083696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49110897-T-G

101083736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49110937-G-A

101083845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49111044-A-G

101083857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49111056-A-G

101083953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49111466-T-C

101083991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49111502-A-G

101084005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49111516-G-T

101084030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49111541-T-G

http://identifiers.org/hco/9/GRCh38#101084072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49111591-C-A

101084079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49111597-G-A

101084298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49114009-G-A

101084641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49114192-G-A

101084641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49114192-G-C

101084641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49114192-G-T

101084691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49114235-T-C

http://identifiers.org/hco/9/GRCh38#101084795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49114325-C-A

101084867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49114388-C-T

http://identifiers.org/hco/9/GRCh38#101084973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49114470-C-A

101085339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49114798-G-A

101085355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49114814-C-G

101085377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49114833-C-T

101085551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49115010-A-G

101085552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49115011-T-C

101085553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49115012-T-C

101085598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49115058-G-A

101085688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49115142-G-A

101085843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49115303-C-T

101085912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49115366-C-T

http://identifiers.org/hco/9/GRCh38#101087329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49116160-C-A

101087478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49116032-C-T

101087813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49115643-A-G

101088618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49117027-A-G

101088711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49117129-C-T

101088762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49117181-G-A

http://identifiers.org/hco/9/GRCh38#101088816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49117236-C-A

101088890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49117310-A-G

101089003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49117418-T-A

101089003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49117418-T-C

101089658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49117807-C-T

101089671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49117820-T-A

101089773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49117905-T-C

101089799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49117931-G-A

101089979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49118096-C-T

101093131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49120748-G-A

101093131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49120748-G-T

101093323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49120939-A-G

101093493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49121108-G-A

101093652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49121266-A-G

101093981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49123582-T-G

101093992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49123593-A-G

http://identifiers.org/hco/9/GRCh38#101094227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49123777-A-C

101094227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49123777-A-G

101094339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49123864-G-C

101094696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49124071-C-T

101094828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49124211-A-G

101094887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49124270-T-C

101094887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49124270-T-G

101094907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49124280-A-T

101095499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49124826-G-A

http://identifiers.org/hco/9/GRCh38#101095867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49125160-C-A

101096015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49125308-G-A

101096036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49125328-A-G

101096203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49125504-A-G

101096243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49125544-G-C

101096245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49125546-G-A

101096245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49125546-G-T

101096251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49125552-G-T

101096262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49125562-A-G

101096301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49125602-G-T

101096526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49125794-C-T

101096610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49125839-G-A

101097104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49126605-C-T

101097168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49126676-G-A

http://identifiers.org/hco/9/GRCh38#101097243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49126749-C-A

101097316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, undefined
orthologous variants: 49126815-A-G

101097381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49126891-G-C

101097447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49126970-T-C

101097941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49127485-G-A

101098164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49127713-C-G

101098289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49127827-G-A

101098295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49127833-C-G

101098545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49127952-A-G

101098773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49128189-T-C

101099290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49128705-T-C

101099920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49128975-T-C

101099949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49129004-A-G

101100141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49129177-G-T

101100218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49129248-T-C

101100265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49129288-T-A

101100766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49129613-T-A

101100818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49129647-G-C

101100928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49129747-G-A

http://identifiers.org/hco/9/GRCh38#101100951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49129770-C-A

101101089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49129900-A-T

101101169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49129953-G-A

101101598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49131749-T-C

101109852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49134182-C-T

101109964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49134282-G-A

101110044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49134378-G-T

101110100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49134426-G-A

101110161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49134483-A-G

101110172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49134495-A-T

101110181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49134504-C-T

101110332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49134636-A-G

101110605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49134900-T-C

101110605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49134900-T-G

101110644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49134938-G-A

101110844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49135163-A-T

101110846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49135165-A-G

101110881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49135197-G-C

101110946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49135260-G-T

101111140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49135445-G-A

101111380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49136170-G-A

101111414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49136205-T-A

101111665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49136420-C-T

101111769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49136527-C-T

101111921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49136681-C-T

101112002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49143125-A-T

http://identifiers.org/hco/9/GRCh38#101112105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49144480-C-A

101112139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49144510-C-T

101112265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49144634-G-T

101112357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49144729-C-T

101112365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49144737-T-C

101112521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49144897-A-G

http://identifiers.org/hco/9/GRCh38#101112571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49144938-C-A

101112572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49144939-A-G

101112816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49145167-G-A

101112964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49145316-A-G

101113368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49146540-G-T

101113462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49146631-A-G

101113462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49146631-A-T

101113579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49146749-G-A

http://identifiers.org/hco/9/GRCh38#101113785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49146903-A-C

101113872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49147028-C-T

101114161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49149355-T-C

101114435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49149612-G-A

101115018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49150150-G-C

101115022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49150154-T-C

101115085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49150215-T-A

101115085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49150215-T-G

101115129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49150258-T-C

101115502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49150580-T-C

101117784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49151684-C-G

101117899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49151771-A-T

http://identifiers.org/hco/9/GRCh38#101118040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49151906-A-C

101118202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49152088-T-C

http://identifiers.org/hco/9/GRCh38#101118533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49152402-C-A

101118563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49152429-T-C

101118635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49152805-T-C

101118734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49153118-C-T

101119089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49153407-G-A

101119131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49153751-T-A

101119147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49153767-C-G

101119148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49153768-C-T

101119241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, undefined
orthologous variants: 49153856-C-T

101119322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, undefined
orthologous variants: 49153941-T-C

101119360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, undefined
orthologous variants: 49153977-C-T

101119365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, undefined
orthologous variants: 49153982-T-G

101119542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49154152-T-C

101119621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49154231-A-G

101119644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49154258-G-C

101119673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49154291-A-T

101119713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49154332-C-T

101119759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49154375-A-G

101119872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49154478-C-G

101119900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49154501-T-C

101119916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49154517-A-G

101120065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49154692-G-A

101120065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49154692-G-T

101120424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49155068-A-G

101120722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49155411-G-C

101121073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49156800-C-T

101121571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49157270-T-C

http://identifiers.org/hco/9/GRCh38#101121706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49157413-A-C

http://identifiers.org/hco/9/GRCh38#101121805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49157502-C-A

101121806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49157503-A-G

http://identifiers.org/hco/9/GRCh38#101121914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49157600-C-A

http://identifiers.org/hco/9/GRCh38#101122258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49157932-C-A

http://identifiers.org/hco/9/GRCh38#101122259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49157933-A-C

101122259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49157933-A-G

101122296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49157971-A-G

101122327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49158005-C-T

http://identifiers.org/hco/9/GRCh38#101122363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49158041-A-C

101122484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49158147-T-G

101122550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49158217-A-T

101123120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49158735-T-C

101123313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49159298-T-G

http://identifiers.org/hco/9/GRCh38#101128071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49159576-A-C

101128161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49159655-G-A

101128353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49159834-A-G

101129897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49160252-T-A

http://identifiers.org/hco/9/GRCh38#101129993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49160340-C-A

http://identifiers.org/hco/9/GRCh38#101130100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49160445-A-C

101130100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49160445-A-G

101130210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49160526-G-A

101130210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49160526-G-T

101130296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49160606-C-T

101130359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49160649-C-T

101130374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49160664-C-T

101130375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49160665-A-G

101130423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49160719-A-G

101130461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49160757-G-A

http://identifiers.org/hco/9/GRCh38#101130748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49161455-C-A

101130774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49161477-G-A

101130807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49161505-G-C

101130939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49161637-G-T

101130940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49161638-G-A

101130950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49161648-A-G

101130954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49161652-A-G

101131113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49161959-C-T

http://identifiers.org/hco/9/GRCh38#101131114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49161960-A-C

101131114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49161960-A-G

101131114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49161960-A-T

101131151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49161990-T-C

101131159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49161998-A-G

101131261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49162116-C-T

101131298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49162153-G-T

101131299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49162154-G-T

http://identifiers.org/hco/9/GRCh38#101131336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49162194-A-C

http://identifiers.org/hco/9/GRCh38#101131383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49162242-C-A

101131586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49162372-C-T

101131587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49162373-A-T

101131595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49162383-G-T

101131630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49162386-G-A

101131630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49162386-G-C

http://identifiers.org/hco/9/GRCh38#101131650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49162406-A-C

101131650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49162406-A-G

101131677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49162429-T-C

101131861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49163843-G-A

http://identifiers.org/hco/9/GRCh38#101131900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49163885-A-C

101131900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49163885-A-G

101131900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49163885-A-T

101131918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49163904-A-G

101131921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49163907-A-G

http://identifiers.org/hco/9/GRCh38#101131951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49163919-C-A

101132008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49163987-G-A

101133165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49166075-T-G

101135340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49166761-G-A

101135450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49166871-C-G

101135570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49166987-G-A

101135639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49167053-G-A

101135661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49167075-A-G

101135661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49167075-A-T

101135706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49167129-C-T

101135780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49167187-C-T

101135826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49167238-A-G

101135826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49167238-A-T

101135862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49167272-C-G

101135881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49167291-G-A

101135931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49167361-A-G

101136177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49167556-G-A

101137495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49168165-A-G

101137638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49168302-A-G

http://identifiers.org/hco/9/GRCh38#101137656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49168320-C-A

101137685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49168350-C-G

101137696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49168361-A-G

101137727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49168380-G-A

http://identifiers.org/hco/9/GRCh38#101137795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49168452-A-C

101137822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49168479-T-C

101137914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49168595-A-G

101138029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49168722-G-A

101138209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49168887-G-T

101138262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49168940-T-C

101138318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49168996-C-T

101138447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49169155-G-A

http://identifiers.org/hco/9/GRCh38#101138527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49169240-A-C

101138599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49169360-A-T

101138800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49170208-C-T

101138818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49170190-A-G

101138877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49170129-C-G

101138879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49170127-A-G

101138955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49170008-G-T

101139052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49169909-T-C

101139321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49169660-A-G

101139338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49169643-G-A

101139338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49169643-G-C

101139367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49169614-C-T

101139456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49169502-A-G

http://identifiers.org/hco/9/GRCh38#101139657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49170453-C-A

101139712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49170495-T-C

101139893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49170694-T-A

101139945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49170721-G-A

101140027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49170787-A-G

http://identifiers.org/hco/9/GRCh38#101140061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49170821-C-A

101140506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49170868-C-G

101140506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49170868-C-T

101140507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49170869-G-A

101140748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49171561-G-A

101140748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49171561-G-T

101140865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49171674-A-T

101141138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49171959-A-G

http://identifiers.org/hco/9/GRCh38#101141335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49172149-A-C

http://identifiers.org/hco/9/GRCh38#101141562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49172359-A-C

101141755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49172543-G-A

101141863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49172655-C-T

101142201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49173041-C-G

101142546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49173389-A-G

101142655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49173506-C-T

101142694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49173544-T-G

101142867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49173688-C-G

101142897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49173721-A-G

101143005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49173848-T-A

101143005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49173848-T-C

101147121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49176705-T-A

101147676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49177302-A-G

101147868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49177485-G-C

101147924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49177545-C-T

http://identifiers.org/hco/9/GRCh38#101148023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49177644-C-A

101148092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49177713-T-G

101148529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49178098-A-G

101148583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49178134-G-A

101148597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49178148-C-T

101150907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49178406-T-A

101150910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49178409-G-A

101150946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49178443-C-T

101150973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49178470-G-A

101150999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49178495-G-A

101151093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49178585-C-G

101151215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49178695-C-G

101151527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49178990-T-C

101151629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49179091-A-G

101151755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49179214-T-C

101151825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49179283-A-T

101156131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49179674-T-G

101156161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49179704-G-T

101156204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49179734-C-G

101156811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49179999-G-A

101156841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49180029-T-A

101157069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49180239-T-C

http://identifiers.org/hco/9/GRCh38#101157105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49180270-C-A

101157375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49180523-T-C

101157392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49180540-G-A

http://identifiers.org/hco/9/GRCh38#101157538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49180785-C-A

101157690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49180952-A-G

101157701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49180963-G-A

101158497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49181866-A-G

101158690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49182032-T-C

101158706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49182048-G-A

101158928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49182265-T-G

101159029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49182375-A-G

101159029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49182375-A-T

101159274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49182648-T-C

101159447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49182783-T-C

101160587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49185181-C-T

101161175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49184584-T-C

http://identifiers.org/hco/9/GRCh38#101161388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49184386-C-A

http://identifiers.org/hco/9/GRCh38#101164838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49183814-C-A

101164992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49183654-T-A

101165491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49183222-A-G

101165683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49191476-C-T

101166176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49194587-G-A

101166648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49195018-C-T

101166756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49195121-T-C

101166962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49195282-G-A

101167076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49195382-A-G

101167089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49195391-A-G

101167113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49195415-G-T

http://identifiers.org/hco/9/GRCh38#101167251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49195482-C-A

101167253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49195484-C-G

101167442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49195666-T-C

101167466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49195689-T-C

101167482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49195705-C-T

http://identifiers.org/hco/9/GRCh38#101168809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49196071-C-A

101168896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49196161-C-T

101169196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49196470-G-A

101169196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49196470-G-C

http://identifiers.org/hco/9/GRCh38#101169269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49196551-C-A

101169269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49196551-C-G

101169427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49196709-G-A

101169596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49196859-T-C

101169931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49197135-C-T

101170031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49197233-A-G

101170151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49197356-C-G

101171395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49197901-G-T

101171460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49197964-C-G

101171471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49197974-G-A

101171548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49198048-G-A

101171938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49198434-G-A

101172880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49199341-A-G

101172909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49199374-T-A

101172953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49199795-A-G

101172973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49199815-C-T

101172976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49199818-A-G

101173015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49199861-C-T

101173179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49200021-G-A

101173476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49200446-T-A

101173698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49200668-C-T

101174291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49201202-G-A

101174291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49201202-G-T

101174607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49201456-C-T

http://identifiers.org/hco/9/GRCh38#101174965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49201785-C-A

101174965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49201785-C-T

101175055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49201878-A-G

101175338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49202144-T-G

101176648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49202240-C-T

101176659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49202251-T-C

http://identifiers.org/hco/9/GRCh38#101176727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49202329-C-A

101176727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49202329-C-T

101176804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49202404-G-T

101176894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49202452-T-C

http://identifiers.org/hco/9/GRCh38#101177045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49202546-A-C

101177154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49202655-C-T

101177188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49202693-G-A

101177285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49202795-C-T

101177289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49202799-C-T

101177301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49202814-C-G

101177467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49202975-T-C

101177569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49203053-C-T

101177975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49203446-G-C

101184165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49203848-T-C

101184310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49205371-A-G

101184317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49205378-G-A

101184317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49205378-G-C

101184331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49205391-G-A

101184505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49205550-T-C

101184576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49205622-T-C

101184710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49205749-A-T

101184729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49205768-G-T

101184892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49205912-A-G

101185059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49206084-G-A

101185059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49206084-G-T

http://identifiers.org/hco/9/GRCh38#101185083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#49206108-C-A

101185083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 49206108-C-G

101185083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 49206108-C-T

101185105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49206129-A-T

101185124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 49206148-T-C

101185148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 49206172-T-C

101185148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 49206172-T-G

http://identifiers.org/hco/9/GRCh38#101185198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49206221-C-A

http://identifiers.org/hco/9/GRCh38#101185221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49206246-C-A

http://identifiers.org/hco/9/GRCh38#101185226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49206251-C-A

101185226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49206251-C-T

101185232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49206257-A-G

101185232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49206257-A-T

101185241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49206266-G-A

101185241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49206266-G-C

101185300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49206301-G-T

101185306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49206307-A-G

101185337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49206336-A-T

http://identifiers.org/hco/9/GRCh38#101185443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49206381-A-C

101185443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49206381-A-G

http://identifiers.org/hco/9/GRCh38#101185456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49206394-C-A

101185456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 49206394-C-T

101185486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 49206424-G-A

101185486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 49206424-G-T

101185579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49206515-T-C

101185643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49206577-A-G

101185852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49206726-G-A

101186111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49206974-T-A

http://identifiers.org/hco/9/GRCh38#101186226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49207062-C-A

101186226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49207062-C-T

101186461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49207291-C-T

101186476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49207305-A-T

101186554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49207380-T-A

101187021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49207882-A-G

http://identifiers.org/hco/9/GRCh38#101187188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49208031-C-A

101187188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49208031-C-T

101187214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49208058-T-A

101187273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49208121-G-T

101187294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49208140-T-A

101187311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49208157-G-T

101187377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49208221-G-A

101187377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49208221-G-T

http://identifiers.org/hco/9/GRCh38#101187378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49208222-C-A

101187378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49208222-C-T

101187380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49208224-A-G

101187449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49208292-G-A

101187482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49208325-G-T

http://identifiers.org/hco/9/GRCh38#101187583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49208420-A-C

101187584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49208421-G-A

101187627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49208462-A-T

101187845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49208682-G-A

101187855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49208692-A-G

101189727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49211597-C-G

101189727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49211597-C-T

101189753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49211623-C-T

http://identifiers.org/hco/9/GRCh38#101190039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49211847-A-C

101190130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49211928-A-G

101190147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49211945-G-T

101190558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49212676-G-A

101190609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49212727-C-T

http://identifiers.org/hco/9/GRCh38#101190815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49212898-A-C

http://identifiers.org/hco/9/GRCh38#101190817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49212900-C-A

101190840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49212923-A-G

101190981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49213027-G-A

101190985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49213030-A-G

101191068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49213100-A-G

101191200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49213215-G-A

http://identifiers.org/hco/9/GRCh38#101191519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49213482-A-C

101191884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49213843-G-T

101191907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49213872-G-A

101192232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49214185-C-T

101192376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49214354-T-A

101192445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49214422-T-C

101192509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49214481-G-C

http://identifiers.org/hco/9/GRCh38#101192644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49214629-A-C

101192644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49214629-A-G

101192782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49214767-T-G

101192924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49214882-G-A

101193099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49215024-G-A

101193099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49215024-G-T

101193249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49215139-G-T

101193778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49215595-C-G

101193989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49216003-T-C

101193994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49216014-C-T

101194002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49216022-C-T

http://identifiers.org/hco/9/GRCh38#101194751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49216711-C-A

101194752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49216712-T-A

101194752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49216712-T-C

101194830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49216737-G-A

101195219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49217056-T-C

101195327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49217156-G-T

101196904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49217815-G-A

101196923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49217834-G-A

101196932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49217843-A-G

http://identifiers.org/hco/9/GRCh38#101196960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49217869-A-C

http://identifiers.org/hco/9/GRCh38#101197032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49217943-A-C

101198020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49220129-G-T

http://identifiers.org/hco/9/GRCh38#101198178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49220312-C-A

101198178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49220312-C-T

http://identifiers.org/hco/9/GRCh38#101198267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49220361-A-C

101198285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49220379-T-A

101198497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49220579-T-C

101198536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49220617-A-G

101200086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49220956-C-G

101200099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49220968-C-T

101200126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49220995-C-T

101200174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49221036-T-C

101200174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49221036-T-G

101200566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49221458-A-G

101200566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49221458-A-T

http://identifiers.org/hco/9/GRCh38#101200714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49221593-C-A

101200714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49221593-C-T

101200956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49222040-C-G

101200956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49222040-C-T

101200995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49222080-G-C

101201044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49222124-C-G

101201495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49222684-G-C

101201657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49222809-C-G

http://identifiers.org/hco/9/GRCh38#101201664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49222816-A-C

101201767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49222920-A-G

101201768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49222921-C-T

101201853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49222986-G-A

101201898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49223031-G-T

101202022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49223157-T-C

101202211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49223346-T-C

101202236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49223371-G-A

101202766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49223555-C-T

101202915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49223695-T-C

101202947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49223727-G-A

101203363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49224303-G-A

101203363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49224303-G-C

101203563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49224485-C-T

http://identifiers.org/hco/9/GRCh38#101203757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49224599-A-C

101203757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49224599-A-T

101203794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49224636-T-A

http://identifiers.org/hco/9/GRCh38#101203936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49224745-A-C

101204041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49224859-G-A

101204041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49224859-G-T

101204268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49225060-C-G

101204289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49225074-G-A

101204357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49225137-G-A

http://identifiers.org/hco/9/GRCh38#101204402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49225199-C-A

101204747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49225504-C-T

101204794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49225559-T-G

101204850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49225617-T-C

101204909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49225682-G-T

101205092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49225854-A-G

http://identifiers.org/hco/9/GRCh38#101205130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49225895-A-C

101205325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49226497-T-C

101205542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49226711-C-T

101205623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49226785-T-A

101205968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49227041-G-C

101205980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49227053-A-G

101206118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49227175-A-T

http://identifiers.org/hco/9/GRCh38#101206294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49227658-C-A

101206356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49227722-C-T

101206379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49227757-G-A

101206418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49227798-G-C

101206534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49227900-T-G

101206544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49227910-T-C

101208448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49227965-A-G

101209828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49229378-A-T

101209948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49229497-G-A

101209955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49229504-T-C

101210069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49229771-G-T

101210226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49229926-T-C

101210285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49229985-C-G

101210448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49230322-C-T

101210632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49230631-C-T

101213318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49231912-T-A

101213320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49231914-A-G

101213350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49231931-T-C

101213682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49232247-G-A

101213746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49232311-G-A

101213823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49232378-G-A

101213825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49232380-A-G

101214129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49232674-G-A

101214129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49232674-G-T

101214278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49232827-G-A

101214437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49232962-T-A

101214445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49232970-C-T

101214460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49232983-T-C

101218897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49236480-A-G

101219056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49236609-C-G

101219056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49236609-C-T

101219061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49236614-A-G

101219074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49236632-G-A

101219074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49236632-G-C

101219077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49236635-C-T

101219510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49237024-C-T

http://identifiers.org/hco/9/GRCh38#101219563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49237081-A-C

101219563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49237081-A-G

101219622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49237140-T-C

101219649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49237168-G-A

http://identifiers.org/hco/9/GRCh38#101219656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49237175-A-C

101219721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49237239-C-G

101219766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49237283-G-T

101221407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49237668-T-A

101221488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49237760-G-A

101221499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49237771-C-T

101221544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49237829-G-A

101221737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49237992-G-A

101221737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49237992-G-C

101221801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49238054-C-T

101222189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49238418-T-C

101222362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49238839-G-A

101222399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49238874-G-A

101222429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49238903-C-G

101222429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49238903-C-T

101222449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49238923-A-G

101222457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49238931-A-G

101222512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49238990-G-C

101222602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49239074-C-T

101222716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49239188-G-A

101223375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49239683-T-C

101223856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49239768-A-G

101224026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49239947-T-C

101224026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49239947-T-G

101224101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49240011-G-A

101224116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49240026-A-G

101224352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49240269-T-G

101224505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49240423-G-A

101224553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49240466-C-T

101224588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49240511-A-G

101225297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49240659-T-C

101225370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49240732-C-T

101225376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49240738-A-G

http://identifiers.org/hco/9/GRCh38#101225421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49240783-C-A

http://identifiers.org/hco/9/GRCh38#101225584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49240944-C-A

101225634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49240977-G-A

101225725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49241060-G-A

101225725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49241060-G-C

101225725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49241060-G-T

101226811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49241633-G-A

101226868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 49241690-A-G

101227011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49241816-G-A

101227147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49241938-G-A

101228117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49242700-G-T

101228219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49242855-T-C

101228272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49242894-G-A

101228283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49242905-G-A

http://identifiers.org/hco/9/GRCh38#101228708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49243692-C-A

101228722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49243706-A-G

101228910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49243891-T-C

101228933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49243907-T-A

101228933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49243907-T-C

http://identifiers.org/hco/9/GRCh38#101228936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49243910-C-A

101229524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49244433-A-T

101229822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49244734-G-A

101229831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49244743-G-A

101230039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49244959-A-G

101230092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49245012-T-C

101230105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49245025-A-G

http://identifiers.org/hco/9/GRCh38#101230302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49245222-A-C

101230357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49245269-A-G

101230443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49245325-G-A

101230523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49245402-C-T

101230727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49245581-G-A

101230737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49245591-G-T

101230842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49245923-G-A

101230842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49245923-G-T

http://identifiers.org/hco/9/GRCh38#101230847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49245928-A-C

101230847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49245928-A-T

101230851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49245932-A-T

101230863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49245944-G-T

101230864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49245945-A-T

101230912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49246101-C-T

http://identifiers.org/hco/9/GRCh38#101231213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49246382-C-A

101231221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49246390-T-C

http://identifiers.org/hco/9/GRCh38#101231237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49246406-A-C

http://identifiers.org/hco/9/GRCh38#101231289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49246454-A-C

http://identifiers.org/hco/9/GRCh38#101231298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49246463-C-A

101231792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49247186-A-T

101231951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49247334-A-T

101232540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49248137-G-A

101232550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49248147-C-G

101233625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49248409-C-T

101234593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49249380-G-A

101234652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49249439-C-G

101234694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49249481-A-T

101234732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49249487-C-T

101235356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49251112-C-G

101235488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49251247-A-G

101235737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49251513-A-T

101235895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49251662-C-G

101236007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49251770-T-A

101236073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49251829-A-T

101236174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49251915-C-T

101236182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49251923-T-C

101236214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49251955-A-G

101236215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49251956-G-A

101236215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49251956-G-T

101236297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49252032-A-T

101236403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49252138-C-T

101242083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49252741-C-T

http://identifiers.org/hco/9/GRCh38#101242087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49252745-C-A

101242087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49252745-C-T

101242266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49252894-G-T

101242274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49252902-A-T

101242612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49253216-G-A

101242929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49253468-T-G

101243024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49253533-T-A

101243061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49253571-G-A

101243428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49253871-G-A

101243428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49253871-G-C

101243583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49254089-G-C

101243626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49254134-A-G

101243798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49254342-T-C

101243807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49254351-G-A

101244197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49255050-G-T

101244209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49255066-G-A

101244257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49255111-A-G

http://identifiers.org/hco/9/GRCh38#101244391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49255248-A-C

101244391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49255248-A-G

101244395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49255252-G-A

101244395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49255252-G-C

101244440-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49255290-T-A

101244750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49255585-T-G

101245320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49256116-A-G

101246148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49258516-G-A

101246148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49258516-G-T

101248159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49259073-G-A

101248298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49259257-C-G

http://identifiers.org/hco/9/GRCh38#101248340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49259299-C-A

101248914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49259846-T-C

101249138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49260049-C-T

101249339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49260245-A-G

101249464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49261258-G-A

101251119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49261399-G-T

101251302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49261570-C-T

101251304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49261572-G-C

101251504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49261766-C-G

101251504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49261766-C-T

101251583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49261855-T-A

101251583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49261855-T-G

101251671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49261925-T-C

101251770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49262032-C-T

101252042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49262286-T-A

101252082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49262330-T-A

101252118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49262366-A-G

101252469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49262573-T-G

101252470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49262574-T-C

101252554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49262638-T-C

101252588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49262672-T-G

http://identifiers.org/hco/9/GRCh38#101252696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49262792-C-A

http://identifiers.org/hco/9/GRCh38#101252730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49262825-C-A

101252829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49262926-G-T

101252835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49262932-T-G

http://identifiers.org/hco/9/GRCh38#101252913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49262995-C-A

101258041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49263490-C-T

101258054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49263504-G-C

101258716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49272879-C-T

101258825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49272973-A-T

101258864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49273026-A-G

101258980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49273154-C-T

101259014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49273188-G-A

101259057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49273229-G-A

101259247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49273621-C-G

http://identifiers.org/hco/9/GRCh38#101262209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49276634-A-C

http://identifiers.org/hco/9/GRCh38#101262259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49276683-A-C

101262270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49276694-G-A

101262304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49276707-G-A

101265140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49278412-T-C

101265235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49278506-G-A

http://identifiers.org/hco/9/GRCh38#101265258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49278529-A-C

101265259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49278530-T-A

101265270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49278536-T-A

101265270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49278536-T-C

101265343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49278609-A-G

101265358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49278624-T-A

101265358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49278624-T-C

101265601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49278855-G-A

101265688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49278941-G-C

http://identifiers.org/hco/9/GRCh38#101265692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49278945-C-A

101266434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49279066-A-G

101266495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49279127-G-A

101266521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49279143-C-T

101266579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49279190-C-T

101267293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49279651-T-C

101267370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49279730-A-G

101267370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49279730-A-T

101267466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49279821-T-C

101267470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49279825-A-G

101267503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49279862-A-T

101267547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49279897-A-G

101267710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49280051-G-A

101267710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49280051-G-C

101268392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49280256-G-A

101268398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49280262-G-T

101268484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49280334-G-C

101268911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49280981-G-A

101268968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49281049-T-C

101269086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49281173-A-T

101269285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49281523-C-T

101269364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49281595-C-T

101269582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49281974-G-A

101269603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49281986-G-C

101269657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49282040-G-T

101269709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49282089-G-A

101269776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49282162-A-G

101269776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49282162-A-T

http://identifiers.org/hco/9/GRCh38#101269786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49282172-C-A

101269786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49282172-C-T

http://identifiers.org/hco/9/GRCh38#101269787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49282173-C-A

101269787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49282173-C-T

101269788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49282174-G-A

101269788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49282174-G-C

101269788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49282174-G-T

101269806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49282188-G-A

101269806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49282188-G-T

101269823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49282205-G-A

101269823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49282205-G-T

101269828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49282210-G-A

101269829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49282211-G-A

101269837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49282219-G-A

http://identifiers.org/hco/9/GRCh38#101269842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49282224-C-A

101269842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49282224-C-T

101269972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49282348-C-T

http://identifiers.org/hco/9/GRCh38#101270152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49282522-C-A

101270219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49282593-T-C

101270296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49282685-G-T

http://identifiers.org/hco/9/GRCh38#101270519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49282903-A-C

101270519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49282903-A-G

101270672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49283045-A-G

101270838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49283200-G-C

101270966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49283338-A-G

http://identifiers.org/hco/9/GRCh38#101271041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49283420-A-C

101271307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49283646-T-C

101271341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49283680-G-A

101271373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49283704-A-G

101271790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49284075-T-C

101272019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49284263-C-G

101274245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49284455-A-G

101274250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49284460-T-A

101274303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49284537-A-G

101274317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49284550-A-G

101274527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49284769-C-T

101274648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49284845-C-T

101274698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49284912-C-T

101275013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49285212-C-G

101275075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49285271-A-G

101275443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49285628-A-G

101275604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49285797-A-G

101275755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49285952-C-G

101275859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49286074-C-T

101275860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49286075-G-A

101275862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49286077-G-A

101275862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49286077-G-T

http://identifiers.org/hco/9/GRCh38#101275864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49286079-A-C

101275864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49286079-A-G

101275866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49286081-G-A

101275878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49286130-T-C

101276043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49286287-T-C

101276043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49286287-T-G

101276118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49286368-C-T

101276256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49286491-T-C

http://identifiers.org/hco/9/GRCh38#101276374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49286616-A-C

101276502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49286764-G-A

101276599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49286873-A-G

101276613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49286888-T-G

101276645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49286920-T-C

101276723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49286989-G-A

101276874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49287130-G-C

101276874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49287130-G-T

101285011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49300117-G-A

101285137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49300211-G-T

http://identifiers.org/hco/9/GRCh38#101285153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49300229-C-A

http://identifiers.org/hco/9/GRCh38#101285181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49300255-C-A

101285259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49300333-G-A

101285421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49300488-G-A

101285430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49300497-T-A

101285431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49300498-A-G

101285431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49300498-A-T

101285831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49300651-A-G

101285929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49300747-T-A

http://identifiers.org/hco/9/GRCh38#101285985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49300799-C-A

101285985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49300799-C-G

101285985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49300799-C-T

101286006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49300827-T-C

101286067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49300883-T-C

101286190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49301007-A-G

101286190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49301007-A-T

101286350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301143-G-A

101286350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301143-G-T

http://identifiers.org/hco/9/GRCh38#101286369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49301182-C-A

101286369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301182-C-T

101286454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301325-A-G

101286545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301411-G-A

101286662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301523-A-G

101286697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301558-G-A

101286698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301559-A-G

101286829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301672-T-C

101287066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301933-G-T

http://identifiers.org/hco/9/GRCh38#101287116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49301975-C-A

101287116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301975-C-T

http://identifiers.org/hco/9/GRCh38#101287227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49302091-A-C

101287228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49302092-T-C

101288058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49302714-T-C

101288060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49302716-G-C

http://identifiers.org/hco/9/GRCh38#101288512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49303694-A-C

101288817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49303921-G-A

101289089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49304473-C-T

101289114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49304498-A-G

101289123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49304507-C-G

101289161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49304544-C-G

101290501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49305601-T-C

101290641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49305718-G-T

101297888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49306715-C-T

101298071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49306885-G-T

101298320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307140-G-A

http://identifiers.org/hco/9/GRCh38#101298420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49307233-A-C

101298533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307348-G-C

101298634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307437-G-A

101298634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307437-G-T

101298777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307609-G-A

101298890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307733-G-A

101299001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307847-T-C

101299096-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49308282-A-T

101299309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49308458-C-T

101299445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49308593-T-C

101299445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49308593-T-G

101299555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49308701-C-G

101299555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49308701-C-T

101300676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49309002-T-C

101301008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49309489-C-T

101301196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49309687-C-T

101301237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49309728-G-A

101301386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49309855-T-C

101301456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49309912-A-G

101306862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49316360-C-T

101306973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49316469-G-A

101307032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49316524-G-T

101307050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49316540-G-A

101307068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49316558-A-G

101307100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49316591-C-T

101307194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49316663-T-C

101307252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49316728-A-G

101307563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49317048-A-G

101308095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49318044-A-G

101308499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49318425-G-T

101308531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49318460-A-G

101308698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49318637-T-G

101308848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49318999-A-G

101308848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49318999-A-T

101308866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49319016-T-C

101308935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49319094-G-A

http://identifiers.org/hco/9/GRCh38#101308948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49319107-C-A

101309034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49319195-C-T

101309061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49319222-A-T

101309096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49319258-T-C

http://identifiers.org/hco/9/GRCh38#101309098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49319270-C-A

101309165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49319714-T-C

101309347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49319897-G-A

101309356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49319906-C-T

101309359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49319909-T-C

101309505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49320055-G-T

101309529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49320080-T-A

http://identifiers.org/hco/9/GRCh38#101309576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49320125-C-A

101309576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49320125-C-T

http://identifiers.org/hco/9/GRCh38#101309704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49320554-C-A

101309704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49320554-C-G

101309704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49320554-C-T

101309864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49320699-C-G

101310105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49320929-G-A

101310151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49320954-G-A

101310259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49321059-T-C

101310284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49321083-T-A

101311211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49321575-T-C

101311405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49321894-A-G

101311422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49321911-A-G

101311948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49322528-C-G

101311948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49322528-C-T

101312085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49322611-C-T

101312229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49322763-G-A

http://identifiers.org/hco/9/GRCh38#101312487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49322981-C-A

101312664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49323152-G-T

101312684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49323172-G-T

http://identifiers.org/hco/9/GRCh38#101312700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49323187-C-A

http://identifiers.org/hco/9/GRCh38#101312733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49323218-C-A

101312733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49323218-C-T

http://identifiers.org/hco/9/GRCh38#101312755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49323235-A-C

http://identifiers.org/hco/9/GRCh38#101312759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49323252-C-A

101312759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49323252-C-T

101312765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49323258-C-T

101312817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49323367-T-C

http://identifiers.org/hco/9/GRCh38#101312823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49323373-C-A

101312823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49323373-C-T

101312824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49323374-G-A

101312834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 49323384-C-T

101312852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49323402-C-T

101312875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49323425-A-G

101312926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: synonymous variant
orthologous variants: 49323476-G-A

101312930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: missense variant
orthologous variants: 49323480-G-A

101312930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: missense variant
orthologous variants: 49323480-G-C

101313068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49323629-T-C

http://identifiers.org/hco/9/GRCh38#101313125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49323682-C-A

http://identifiers.org/hco/9/GRCh38#101313146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49323702-C-A

101313146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49323702-C-T

101315514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, undefined
orthologous variants: 49324201-C-T

http://identifiers.org/hco/9/GRCh38#101315763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#49324430-C-A

101315962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49324608-A-G

101316065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49324710-T-C

101316103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49324731-C-T

101316341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49324786-G-A

http://identifiers.org/hco/9/GRCh38#101316436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49324826-C-A

101316522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49324857-G-A

101316523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49324858-G-A

101316523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49324858-G-C

101316546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49324881-T-A

101316546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49324881-T-C

http://identifiers.org/hco/9/GRCh38#101316590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49324939-C-A

101316611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49324952-T-A

http://identifiers.org/hco/9/GRCh38#101316631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49324958-A-C

101316771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49325057-A-T

101316933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49325179-C-T

101317026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49325278-G-A

http://identifiers.org/hco/9/GRCh38#101317045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49325297-C-A

101317160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49325405-C-T

101317281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49325535-A-T

101317290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49325544-G-A

101317290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49325544-G-T

http://identifiers.org/hco/9/GRCh38#101317298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49325552-C-A

101317298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49325552-C-G

101319409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49327105-C-T

101319433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49327129-A-G

http://identifiers.org/hco/9/GRCh38#101320132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49327685-A-C

101320158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49327721-G-A

101320251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49327804-G-C

101320337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49327881-A-G

http://identifiers.org/hco/9/GRCh38#101320462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49328013-A-C

101320525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49328087-T-C

101320579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49328141-C-T

101321171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49335999-T-C

101321520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron variant
orthologous variants: 49336298-G-T

101324005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: intron_variant, undefined
orthologous variants: 49337627-T-C

101324033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: synonymous_variant, undefined
orthologous variants: 49337654-T-C

101324065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 49337686-G-A

101324162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 49337810-A-G

101324171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 3 prime UTR variant
orthologous variants: 49337819-G-C

101324171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 3 prime UTR variant
orthologous variants: 49337819-G-T

101324205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 49337853-A-G

101324205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 49337853-A-T

http://identifiers.org/hco/9/GRCh38#101324299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49337940-A-C

101324332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 49337973-G-C

101324332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 49337973-G-T

http://identifiers.org/hco/9/GRCh38#101324337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#49337978-C-A

101324337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 49337978-C-T

101324395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 3 prime UTR variant
orthologous variants: 49338035-A-G

101324396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 3 prime UTR variant
orthologous variants: 49338036-T-A

101324396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 3 prime UTR variant
orthologous variants: 49338036-T-C

101324498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 49338138-G-A

101324498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 49338138-G-T

101325062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25993
most severe consequence: 3 prime UTR variant
orthologous variants: 49338700-A-G