http://identifiers.org/hco/13/GRCh38#35768959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55446499-C-A

35769336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55446127-C-T

35769346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55446117-C-T

35769560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55445901-G-T

35769780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55445702-G-A

35769780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55445702-G-T

35770194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55445299-A-G

http://identifiers.org/hco/13/GRCh38#35770288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55445205-C-A

35770497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55445001-G-A

35770497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55445001-G-C

35770636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55444851-T-C

35770807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55444628-A-G

35770977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55444467-A-G

35771062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55444382-C-G

35771062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55444382-C-T

http://identifiers.org/hco/13/GRCh38#35771065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55444379-A-C

35771066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55444378-A-T

35771067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55444377-G-A

35771067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55444377-G-T

35771300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55444136-G-T

35771301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55444135-C-T

35771372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55444063-T-A

http://identifiers.org/hco/13/GRCh38#35771393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55444042-C-A

http://identifiers.org/hco/13/GRCh38#35771479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55443954-C-A

35772218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 55443245-G-A

35772433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55443078-G-T

http://identifiers.org/hco/13/GRCh38#35772552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55442973-C-A

http://identifiers.org/hco/13/GRCh38#35772566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55442959-C-A

35772566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55442959-C-T

35772966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55442633-T-C

35773098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55442530-G-A

35773226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55442427-A-G

35773265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55442388-C-T

35773326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55442326-T-C

35773459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55442217-T-C

http://identifiers.org/hco/13/GRCh38#35773902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55441790-C-A

http://identifiers.org/hco/13/GRCh38#35773946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55441746-C-A

35773947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55441745-T-G

35774291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55441403-A-T

35774293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55441401-T-A

35774293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55441401-T-C

35774293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55441401-T-G

http://identifiers.org/hco/13/GRCh38#35774421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55441271-C-A

35774421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55441271-C-T

35774476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55441217-G-A

35774476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3 prime UTR variant
orthologous variants: 55441217-G-T

http://identifiers.org/hco/13/GRCh38#35774738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55440950-C-A

35774738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55440950-C-T

http://identifiers.org/hco/13/GRCh38#35774799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55440893-C-A

35774799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55440893-C-G

35774810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55440882-T-A

35774825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55440867-A-G

35775258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55440555-G-A

35775555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55440233-G-A

35775600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55440189-A-T

35775614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55440175-G-A

35775615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55440174-T-A

35775947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55439827-A-G

35776559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55439216-A-G

35776647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55439119-G-T

35776777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55439003-C-T

35776882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55438817-C-G

35777053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55438666-G-A

35777587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55438205-T-A

35777607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55438189-T-C

35777628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55438166-C-T

35777904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55437925-T-A

35777919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55437909-C-T

35777982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55437853-C-G

http://identifiers.org/hco/13/GRCh38#35778005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55437832-C-A

35778014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55437823-T-C

35778014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55437823-T-G

35778041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55437796-A-G

35779699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55436564-G-A

35779831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55436441-G-A

35779832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55436440-C-T

35779848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55436424-A-G

35779848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55436424-A-T

35779849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55436423-T-C

35779967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55436309-A-T

35779976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55436300-C-G

35779976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55436300-C-T

35780833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55435555-T-G

35780881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55435506-C-T

35781148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55435264-G-T

35781213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55435196-T-C

35781281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55435129-T-C

35781381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55435029-A-G

http://identifiers.org/hco/13/GRCh38#35781794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55434632-C-A

35781794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55434632-C-T

35782394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55434073-A-G

35782395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55434072-T-A

35782398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55434069-T-G

35782497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55433961-A-G

35782664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55433792-T-A

35782829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55433662-G-T

35782837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55433653-G-A

35782837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55433653-G-C

35782907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55433591-C-G

35782934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55433573-G-A

35782934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55433573-G-T

35782957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55433550-T-G

35782981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55433526-T-C

35784222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55433340-G-C

35784451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55433085-C-T

35785086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55432334-G-A

35785086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55432334-G-C

35785146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55432256-T-C

35785314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55432089-C-T

http://identifiers.org/hco/13/GRCh38#35785660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#55431748-C-A

http://identifiers.org/hco/13/GRCh38#35785749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55431659-C-A

35785811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55431596-T-C

http://identifiers.org/hco/13/GRCh38#35786309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55431085-C-A

35787026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55430493-T-C

35787064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55430456-G-C

http://identifiers.org/hco/13/GRCh38#35787162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55430386-A-C

35787364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55430186-T-C

35787457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55430090-G-A

35787461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55430086-G-C

35787701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55429857-C-T

http://identifiers.org/hco/13/GRCh38#35787866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55429691-C-A

http://identifiers.org/hco/13/GRCh38#35787880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55429677-C-A

35787880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55429677-C-G

35788435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55429115-T-A

35788435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55429115-T-C

35788456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55429093-A-G

35788523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55429021-T-C

35788808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55428755-T-C

35788817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55428746-T-G

35788965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55428630-C-T

35789161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55428450-G-T

35789167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55428445-G-A

35789534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55428090-T-C

35789773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55427853-G-A

35789829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55427801-T-C

35789900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55427718-A-T

35790248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55427365-A-G

http://identifiers.org/hco/13/GRCh38#35790362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55427248-A-C

35790397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55427217-C-G

35790459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55427145-C-T

35790508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55427102-T-G

35790551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55427063-A-G

35790574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55427034-G-A

35790633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55426980-T-C

35790692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55426921-C-G

35791482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55426143-G-A

35791491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55426129-T-C

35791547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55426090-T-C

35792268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55425411-G-A

35792614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55425100-T-C

http://identifiers.org/hco/13/GRCh38#35792878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55424840-A-C

35792909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55424807-G-A

35792929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55424788-G-T

35793021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55424695-T-C

35793085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55424649-G-C

http://identifiers.org/hco/13/GRCh38#35793224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55424526-C-A

35793227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55424523-C-T

35793347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55424424-G-A

35793541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55424224-G-A

35793541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55424224-G-T

http://identifiers.org/hco/13/GRCh38#35793543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55424222-C-A

35793692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55424068-T-C

35793717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55424043-C-G

35793717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55424043-C-T

35793828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55423944-T-C

35793829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55423943-T-G

35793928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55423864-C-T

35793996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55423795-A-T

35794188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55423647-G-A

35794195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55423640-C-T

35794301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55423533-C-T

35794703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55423097-G-A

35794703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55423097-G-T

35794716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55423084-C-T

35794747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55423055-A-T

35795112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55422433-A-G

http://identifiers.org/hco/13/GRCh38#35795116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55422429-C-A

35796066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55421636-G-A

35796220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55421467-G-T

35796259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55421426-G-A

35796263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55421422-T-C

35796371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55421345-G-C

35796477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55421250-A-G

35796538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55421183-G-A

35796551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55421170-G-T

35796834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55420887-G-A

35796943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55420777-A-G

35796974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55420746-A-G

35796976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55420739-T-C

35796977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55420738-G-A

35797070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55420644-T-G

35797438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55420330-T-G

35797745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55419674-G-A

35797756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55419663-C-T

35798281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55419154-T-C

35798418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55419018-A-T

35798491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55418945-T-C

35799032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55418458-A-G

35799227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55418283-G-A

35799241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55418269-G-A

35799812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55418005-A-T

35799944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55417881-T-G

35799948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55417877-G-A

35799961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55417864-G-C

35800162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55417699-C-T

35800166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55417695-T-C

35800326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55417553-T-G

http://identifiers.org/hco/13/GRCh38#35800501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55417385-C-A

35800501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55417385-C-T

35800546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55417352-A-G

http://identifiers.org/hco/13/GRCh38#35800612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55417280-A-C

35800631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55417260-C-T

http://identifiers.org/hco/13/GRCh38#35801417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55416812-C-A

35801417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55416812-C-T

35802010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55416263-T-C

http://identifiers.org/hco/13/GRCh38#35802121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55416184-C-A

35802901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55415953-A-G

35802926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55415928-G-A

35803124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55415736-G-A

http://identifiers.org/hco/13/GRCh38#35803128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55415732-A-C

35803347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55415495-G-A

35803485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55415365-T-G

35803486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55415364-G-T

35803505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55415345-T-C

35803528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55415322-T-A

35803652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55415199-T-C

35803710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55415144-T-C

35803710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55415144-T-G

35804869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55414663-A-T

35804929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55414606-G-C

35804973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55414574-T-G

35805600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55414295-A-G

35805600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55414295-A-T

35805794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55414106-G-A

35805794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55414106-G-C

35805800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55414100-G-T

35805869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55414018-A-G

35805876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55414011-T-C

35805876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55414011-T-G

http://identifiers.org/hco/13/GRCh38#35805885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55414002-C-A

35805885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55414002-C-T

http://identifiers.org/hco/13/GRCh38#35805887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55414000-C-A

35805888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55413999-T-C

35805905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55413983-A-G

http://identifiers.org/hco/13/GRCh38#35805907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55413981-C-A

35805907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55413981-C-T

35805913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55413975-T-C

35805913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55413975-T-G

35805918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55413970-T-A

35805918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55413970-T-C

35805976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55413902-A-G

35805994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55413875-A-G

35806007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55413847-T-C

35806142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55412862-T-C

35806200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55412810-T-C

35806243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55412767-G-T

http://identifiers.org/hco/13/GRCh38#35806539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55412649-A-C

35806539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55412649-A-G

35806761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55412417-C-T

35806920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55412135-A-G

35807210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55411513-T-G

35807372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55411354-C-T

35807476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55411258-G-A

35807730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55410839-T-G

35807917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55410586-T-C

http://identifiers.org/hco/13/GRCh38#35808103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55410445-C-A

35808103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55410445-C-T

35808110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55410439-G-A

35808110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55410439-G-T

35808146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55410406-T-G

35808197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55410351-G-T

http://identifiers.org/hco/13/GRCh38#35808349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55410206-A-C

35808349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55410206-A-G

35808361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55410195-T-C

35808361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55410195-T-G

35808401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55410157-G-A

35808401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55410157-G-T

35808410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55410150-T-C

http://identifiers.org/hco/13/GRCh38#35808412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55410148-C-A

35808412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55410148-C-T

http://identifiers.org/hco/13/GRCh38#35808422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55410138-A-C

35808427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55410133-T-A

35808716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55410066-G-A

35808934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55409953-T-C

http://identifiers.org/hco/13/GRCh38#35808935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55409952-C-A

35808935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55409952-C-T

http://identifiers.org/hco/13/GRCh38#35809240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55409656-C-A

35810390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55408010-C-T

35810628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55407766-T-G

35810650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55407751-T-C

35810661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55407740-G-C

35810675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55407731-C-G

35810727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55407675-T-C

35810728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55407674-G-T

35810730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55407672-T-G

http://identifiers.org/hco/13/GRCh38#35811009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55407412-A-C

35811094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55407366-G-A

35811094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55407366-G-T

35811096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55407364-A-G

35811098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55407362-G-A

35811098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55407362-G-T

35811106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55407354-A-G

35811106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55407354-A-T

35811265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55407296-T-A

35811370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55407210-T-C

35812353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55406626-T-A

35812357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55406622-A-G

35812663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55406346-G-C

35812752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55406237-A-T

35812999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55406034-G-A

35813027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55406019-T-C

http://identifiers.org/hco/13/GRCh38#35813251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55405794-A-C

35813545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55405509-T-A

http://identifiers.org/hco/13/GRCh38#35813553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55405482-A-C

35813604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55405425-G-A

35813604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55405425-G-T

35813605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55405424-A-G

35813607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55405422-T-C

35813733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55405303-T-A

35813756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55405286-A-T

http://identifiers.org/hco/13/GRCh38#35813782-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55405260-A-C

http://identifiers.org/hco/13/GRCh38#35813783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55405259-C-A

35813875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55405163-T-A

35813875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55405163-T-C

35813999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55405038-C-T

35814408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55404663-C-T

35814456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55404530-T-A

35814470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55404516-G-T

35814551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55404322-G-A

35814767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55404108-T-C

35814953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55403922-T-C

35815217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55403720-G-C

35815473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55403469-T-G

35815651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55403292-T-G

35815985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55402936-T-C

35816285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55402652-A-G

35818949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55401376-G-A

35819222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55401143-A-G

35819288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55401091-T-G

35819420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55400961-G-A

http://identifiers.org/hco/13/GRCh38#35819529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55400850-A-C

35819591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55400788-C-T

35819600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55400780-A-G

35819745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55400632-A-G

35820216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55400226-T-C

35820411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55400014-C-T

35820446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55399983-G-C

35820767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55399667-T-G

35821098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55399371-C-T

35821247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55399215-C-T

35821771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55398721-C-T

35821868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55398631-G-T

http://identifiers.org/hco/13/GRCh38#35821964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55398315-A-C

35822051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55398235-T-C

35822708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55397336-T-C

35822916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55397129-G-A

35822916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55397129-G-T

35822939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55397107-G-A

35822940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55397106-G-A

35822940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55397106-G-T

http://identifiers.org/hco/13/GRCh38#35822983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55397064-C-A

35823349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55396713-T-C

35823360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55396695-C-T

http://identifiers.org/hco/13/GRCh38#35823854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55396184-C-A

35823854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55396184-C-T

35823937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55396110-C-T

35823950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55396097-T-A

35825607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55395662-A-T

35825633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55395635-C-T

35827663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: missense variant
orthologous variants: 55395302-T-C

35827663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: missense variant
orthologous variants: 55395302-T-G

35827705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: missense variant
orthologous variants: 55395260-G-A

35827763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55395202-A-G

35827821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55395148-A-G

35827845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55395130-G-A

35827845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55395130-G-T

35827883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55395102-A-G

35828010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55395015-C-T

35828100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55394926-T-C

35828113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55394911-A-G

35828123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55394901-G-T

http://identifiers.org/hco/13/GRCh38#35828165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55394860-A-C

35828199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55394832-C-T

http://identifiers.org/hco/13/GRCh38#35828324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55394709-C-A

35828324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55394709-C-T

35828325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55394708-A-G

35828369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55394647-T-C

35828428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55394596-A-G

35828445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55394580-T-C

35828858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55394211-T-C

35828870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55394198-C-T

35828959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55394121-C-G

35829169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55393930-G-A

35829171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55393928-C-T

35829244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55393870-T-A

http://identifiers.org/hco/13/GRCh38#35829275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55393839-A-C

35829472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55393651-T-C

35829530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55393633-C-T

35829587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55393571-G-A

35829587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55393571-G-C

35829775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55393396-G-A

35829779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55393392-T-C

35829808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55393362-C-T

35829860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55393310-G-A

35830048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55393137-G-A

35830405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55393058-T-G

35830697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55392847-A-T

35830888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55392703-C-T

35830964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55392634-G-A

35831036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55392574-G-T

35831060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55392550-C-T

http://identifiers.org/hco/13/GRCh38#35831162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55392451-C-A

35831591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55392198-G-A

35833642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55391115-G-A

35833756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55391002-G-A

35833756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55391002-G-T

http://identifiers.org/hco/13/GRCh38#35834250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55389587-C-A

35834639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55389203-G-A

35834661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55389180-T-G

35834662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55389179-G-A

35834700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55389139-G-C

35835215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55388681-G-A

35835279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55388629-T-G

35835468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55388467-T-C

35835500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55388435-A-G

35835826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55388044-T-C

35836010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55387884-G-C

http://identifiers.org/hco/13/GRCh38#35836152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55387742-C-A

35836152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55387742-C-T

35836237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55387656-G-T

35836279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55387636-G-A

35836279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55387636-G-T

35836526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55387393-C-T

35837235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55386712-G-A

35837235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55386712-G-C

35837291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55386670-C-T

35837318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55386643-C-T

35837555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55386392-A-G

http://identifiers.org/hco/13/GRCh38#35838285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55386054-A-C

35838293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55386046-C-T

35838452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55385894-T-C

35838452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55385894-T-G

35838453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55385893-A-G

35838527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55385821-A-T

35838566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55385783-A-G

35838689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55385650-T-C

http://identifiers.org/hco/13/GRCh38#35838945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55385460-C-A

35838991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55385413-G-T

35839019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55385386-G-A

35839019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55385386-G-T

http://identifiers.org/hco/13/GRCh38#35839103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55385297-C-A

35839118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: missense variant
orthologous variants: 55385282-A-G

35839121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: missense variant
orthologous variants: 55385279-G-A

35839121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: missense variant
orthologous variants: 55385279-G-C

35839121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: stop gained
orthologous variants: 55385279-G-T

http://identifiers.org/hco/13/GRCh38#35839127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55385273-C-A

35839127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: missense variant
orthologous variants: 55385273-C-T

35839134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: stop gained
orthologous variants: 55385266-T-A

35839145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: missense variant
orthologous variants: 55385255-A-G

35839463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55384952-G-A

35839577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55384852-C-G

35839749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55384675-T-C

35840490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55383969-G-A

35840547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55383915-G-C

35840547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55383915-G-T

35840602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55383860-T-A

35840811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55383636-C-T

35841009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55383441-A-G

35841058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55383391-A-T

35841155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55383263-G-A

35841326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55382997-C-T

35841741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55382596-A-G

35841773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55382564-A-T

35841845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55382487-G-A

http://identifiers.org/hco/13/GRCh38#35843878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55380250-A-C

35843886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55380242-T-C

35844074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55380051-G-C

35844074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55380051-G-T

http://identifiers.org/hco/13/GRCh38#35844244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55379923-A-C

35844246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55379921-T-G

35844660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55379553-A-G

35844688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55379525-C-T

35844721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55379499-A-G

35844721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55379499-A-T

35844736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55379484-C-T

35845494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55379112-C-T

35845593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55379015-C-T

35845731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55378884-C-T

35845808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55378813-G-A

35845808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55378813-G-T

http://identifiers.org/hco/13/GRCh38#35845824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55378797-C-A

35845824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55378797-C-T

35845921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55378716-T-A

35845921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55378716-T-C

35845921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55378716-T-G

35846201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55378430-T-C

35846240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55378399-T-C

35846467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55378172-T-C

http://identifiers.org/hco/13/GRCh38#35846489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55378150-C-A

35846593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55378040-A-G

http://identifiers.org/hco/13/GRCh38#35846686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55377947-C-A

35846686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55377947-C-T

35846738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55377895-G-T

35846809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55377825-A-G

35846809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55377825-A-T

35846834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55377800-A-G

35846839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55377795-G-A

35847043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55377594-A-G

35847098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55377549-T-C

35847105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55377542-C-T

35847109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55377538-C-T

http://identifiers.org/hco/13/GRCh38#35847201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55377406-C-A

35847201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55377406-C-T

35847325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55377281-A-G

35847597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55376999-G-A

35847597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55376999-G-C

35847676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55376954-T-C

35847716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55376915-A-G

35847723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55376908-G-A

35847723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55376908-G-T

35847767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55376870-G-C

35847777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55376860-T-C

http://identifiers.org/hco/13/GRCh38#35847821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55376815-A-C

35847821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55376815-A-T

35847824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55376812-T-C

35848011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55376652-C-T

35848058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55376608-T-A

35848058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55376608-T-C

http://identifiers.org/hco/13/GRCh38#35848142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55376533-A-C

35848247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55376425-A-G

35848315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55376367-A-G

35848344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55376336-T-C

35848616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55376075-T-C

35848634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55376057-T-A

35848864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55375859-A-G

http://identifiers.org/hco/13/GRCh38#35848878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55375842-C-A

http://identifiers.org/hco/13/GRCh38#35848980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55375740-C-A

35848980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55375740-C-G

35848980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55375740-C-T

http://identifiers.org/hco/13/GRCh38#35849535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55375192-A-C

35849535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55375192-A-G

http://identifiers.org/hco/13/GRCh38#35849658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55375080-A-C

http://identifiers.org/hco/13/GRCh38#35849825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55374924-C-A

35849936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55374822-T-A

35849956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55374802-C-T

35850188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55374598-A-T

http://identifiers.org/hco/13/GRCh38#35850386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55374382-C-A

35850460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55374307-G-A

35850460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55374307-G-T

http://identifiers.org/hco/13/GRCh38#35850500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55374256-C-A

35850526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55374229-T-G

http://identifiers.org/hco/13/GRCh38#35850574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55374181-C-A

35850574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55374181-C-T

http://identifiers.org/hco/13/GRCh38#35850579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55374176-A-C

35850579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55374176-A-G

35850579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55374176-A-T

35850580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55374175-T-C

35850580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55374175-T-G

35851044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55373743-C-T

35851321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55373490-T-C

35851363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55373454-A-G

35851993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55372847-G-A

http://identifiers.org/hco/13/GRCh38#35852988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55371881-A-C

35853011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55371856-G-A

35853023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55371847-G-A

35853023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55371847-G-C

35853530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55371475-T-C

http://identifiers.org/hco/13/GRCh38#35853699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55371306-C-A

35853717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55371287-G-A

http://identifiers.org/hco/13/GRCh38#35853734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55371270-C-A

35853734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55371270-C-G

35853734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55371270-C-T

35853742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55371262-G-A

http://identifiers.org/hco/13/GRCh38#35854630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55370383-C-A

35854630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55370383-C-T

35854655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55370358-T-C

35854725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55370296-T-C

35854725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55370296-T-G

http://identifiers.org/hco/13/GRCh38#35854728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55370293-A-C

35854728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55370293-A-G

35854841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55370175-T-C

35855479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55369535-A-G

35855560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55369448-A-G

35855630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55369367-G-C

35855630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55369367-G-T

35855775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55369221-T-A

35855775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55369221-T-C

35855872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55369107-G-A

35855872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55369107-G-T

35856346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55368637-G-T

35860005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55365148-T-C

35860133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55365024-A-G

35860331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55364850-A-G

http://identifiers.org/hco/13/GRCh38#35860636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55364167-C-A

35860636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55364167-C-T

35862209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55363566-G-A

35862215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55363561-G-A

http://identifiers.org/hco/13/GRCh38#35862572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55363232-C-A

35862572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55363232-C-T

35863477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55362595-G-T

35864949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55361483-G-A

35865108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55361314-C-T

35869202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55360451-G-T

35869209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55360444-T-C

35869238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55360415-T-C

35869644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55360168-C-T

35869983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55359847-T-C

http://identifiers.org/hco/13/GRCh38#35870041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55359797-C-A

35870260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55359542-G-C

35870311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55359515-G-C

http://identifiers.org/hco/13/GRCh38#35870541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55359317-C-A

35870564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55359292-A-T

35870750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55358972-G-A

35870969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55358756-A-G

35871004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55358722-C-G

35871024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55358703-A-G

35871111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55358615-T-C

35871214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55358512-G-A

35871214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55358512-G-T

http://identifiers.org/hco/13/GRCh38#35871427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55358367-A-C

35871660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55358223-T-G

35871667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55358216-A-G

35871691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55358192-T-A

35871710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55358176-A-T

35871935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55357971-C-T

35872023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55357889-T-C

35872257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55357676-A-T

35873929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55356340-T-G

35873986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55356266-T-C

35874077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55356060-T-C

35874340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55355869-A-G

35875107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55355355-T-A

35875259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55355226-A-G

35875426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55355064-T-C

35875525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55354951-C-G

35875723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55354815-C-T

http://identifiers.org/hco/13/GRCh38#35875757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55354781-A-C

35876000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55354540-G-A

35876492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55354095-A-G

35876666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55353912-A-G

35876965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55353652-C-T

35877499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55351158-C-G

35877519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55351138-C-T

35877560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55351097-A-G

35877782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55350894-G-T

35877868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55350806-T-C

35877971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55350695-G-A

35878118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55350571-C-T

35879213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55350050-T-C

35879397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55349881-G-A

35879397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55349881-G-C

35879435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55349845-A-G

35879828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55349484-G-A

35879860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55349452-A-T

35879937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55349381-T-C

35880089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55349233-G-A

35880270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55349123-G-A

http://identifiers.org/hco/13/GRCh38#35880460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55348929-A-C

35880534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55348863-G-A

35880573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55348824-T-C

35880649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55348767-G-A

35880649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55348767-G-C

35880661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55348755-C-T

35881029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55348376-T-C

35881305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55348108-G-A

35881305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55348108-G-C

35881327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55348086-T-A

35881386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55348024-C-G

35881400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55348010-C-T

35881473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55347938-G-A

35881629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55347788-C-T

35882445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55347579-A-G

http://identifiers.org/hco/13/GRCh38#35882529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55347513-C-A

35882701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55347361-C-T

35882706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55347356-C-G

35882706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55347356-C-T

35882811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55347277-A-G

35883768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55346798-G-A

35883821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55346748-A-G

35883836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55346720-A-T

35883998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55346563-T-A

35884039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55346522-G-A

http://identifiers.org/hco/13/GRCh38#35884074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55346494-C-A

35884074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55346494-C-T

35884089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55346479-G-C

35884298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55346274-T-A

35884451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55346145-T-A

http://identifiers.org/hco/13/GRCh38#35884496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55346098-A-C

http://identifiers.org/hco/13/GRCh38#35884519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55346075-A-C

http://identifiers.org/hco/13/GRCh38#35884621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55345979-A-C

35884847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55345767-T-G

35884961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55345644-C-G

35885424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55344681-T-C

35885629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55344535-G-C

35886400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55344236-C-T

35886443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55344193-G-A

35886445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55344190-G-A

35886477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55344144-G-A

35886495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55344126-C-T

35886606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55344033-T-C

35886622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55344018-A-G

35887203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55343584-G-A

35887347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55343450-T-C

35887532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55343315-T-C

35887962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55342484-C-T

35888066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55342396-T-C

35888167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55342294-T-C

35888484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341980-C-T

35888581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341883-G-A

35888619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341846-G-A

35888645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341821-G-T

35889016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341463-A-G

35889139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341353-T-G

35889275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341224-T-C

35889500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341025-T-A

35889836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55340894-G-A

35889987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55340763-A-T

http://identifiers.org/hco/13/GRCh38#35889992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55340758-C-A

35889992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55340758-C-T

35890098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55340645-A-G

35890178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55340580-T-C

35890298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55340486-G-A

35890502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55340352-T-C

35890549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55340305-A-T

35890653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55340194-T-C

35890715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55340135-C-T

35890749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55340102-G-A

35890863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55339988-C-T

35890870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55339981-T-C

35891180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55339701-C-T

35891211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55339670-T-C

35891499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55339334-T-C

35891750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55339101-C-T

35891789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55339077-T-A

http://identifiers.org/hco/13/GRCh38#35891882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55338986-A-C

http://identifiers.org/hco/13/GRCh38#35892287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55338615-A-C

http://identifiers.org/hco/13/GRCh38#35892306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55338596-C-A

35892814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55338111-C-T

35892961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55337956-A-G

35893267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55337249-A-G

35893357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55337164-C-T

35894254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55337025-A-G

35894265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55337017-G-A

35894326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55336964-G-A

35894522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55336800-A-G

35894647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55336727-C-T

35894738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55336559-C-T

35895303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55336332-T-A

35895484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55335911-T-C

35895510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55335881-A-G

35895529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55335862-C-G

35895538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55335851-A-G

35895551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55335838-A-G

35895593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55335797-T-C

http://identifiers.org/hco/13/GRCh38#35895872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55335523-A-C

35895872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55335523-A-T

35895961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55335432-A-T

35896159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55335253-C-T

35896181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55335233-G-C

35896988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55334279-A-T

35897326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55334027-C-G

35897388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55333963-G-T

35897472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55333891-G-T

35897522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55333842-C-T

35897987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55333387-A-G

http://identifiers.org/hco/13/GRCh38#35898351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55333048-C-A

35898364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55333035-G-A

35898470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55332935-T-C

35899253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55331826-A-G

http://identifiers.org/hco/13/GRCh38#35899259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55331820-C-A

http://identifiers.org/hco/13/GRCh38#35899327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55331760-C-A

35899327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55331760-C-T

35899368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55331751-T-A

35899372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55331747-A-T

35899433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55331686-C-G

35899503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55331621-C-G

35899535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55331589-G-C

35899797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55331157-A-G

35899955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55330928-T-C

35899973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55330915-G-T

35900104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55330768-G-A

35900104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55330768-G-T

35900699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55330512-G-A

35900835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55330394-T-C

35900870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55330364-A-G

http://identifiers.org/hco/13/GRCh38#35900962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55330278-C-A

35900962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55330278-C-T

35901034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55330212-G-C

35901129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55330131-C-T

35901146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55330114-T-C

35902443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55328989-A-G

35902486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55328955-A-G

35902754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55328763-G-A

35903080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55328440-T-C

35903255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55328320-T-C

35903344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55328227-C-T

http://identifiers.org/hco/13/GRCh38#35903654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55327543-C-A

35903815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55327390-C-T

35907784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55325674-G-A

35907820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55325628-T-A

35907859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55325589-G-A

35908005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55325448-T-A

http://identifiers.org/hco/13/GRCh38#35908009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55325444-C-A

35908009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55325444-C-T

35908082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55325400-T-C

35908210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55325279-T-C

http://identifiers.org/hco/13/GRCh38#35909152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55324499-C-A

35909152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55324499-C-T

http://identifiers.org/hco/13/GRCh38#35909663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55323571-A-C

35909663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55323571-A-G

http://identifiers.org/hco/13/GRCh38#35909665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55323569-A-C

35909665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55323569-A-G

35909706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55323534-G-A

35909891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55323385-C-T

35909965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55323304-C-T

35910014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55323237-G-T

35910061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55323193-G-A

35910284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55322977-T-C

35910412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55322860-G-T

35910654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55322680-C-T

35910676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55322660-C-T

35910697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55322637-G-T

35910790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55322543-T-A

35910790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55322543-T-C

35910851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55322496-T-C

http://identifiers.org/hco/13/GRCh38#35910912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55322433-C-A

35911370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55322303-C-T

35917435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55321164-G-A

35917435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55321164-G-C

35917502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55321125-T-A

35917889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55320743-A-G

35918139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55320517-C-T

35918318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55320203-T-C

35919367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55318945-A-G

35919494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55318818-C-T

35920138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55318399-C-T

35920293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55317563-G-C

35920425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55317441-T-G

35920773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55317140-C-T

35920785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55317128-C-T

35920980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55316914-C-T

http://identifiers.org/hco/13/GRCh38#35920983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55316911-C-A

35920983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55316911-C-T

35921071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55316838-C-G

35921105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55316802-T-A

35921348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55316584-T-A

35921366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55316566-C-T

35921388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55316548-T-C

35921399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55316534-A-T

35921454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55316476-T-A

http://identifiers.org/hco/13/GRCh38#35921455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55316475-C-A

35921455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55316475-C-T

35921621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55316319-A-G

35921935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55315605-G-A

35921976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55315577-C-T

35922243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55315320-G-A

35922402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55315182-G-A

35922523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55315062-C-G

35922595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55314993-A-G

35922934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55309305-C-G

35923387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55309023-T-C

35923909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55308181-C-T

35924817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55305942-T-A

35924817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55305942-T-C

35925017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55305785-A-T

35925400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55305383-T-A

35925400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55305383-T-C

35925410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55305373-G-A

35925410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55305373-G-C

35925709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55305065-T-C

35925804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55304994-T-C

35926026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55304790-G-A

http://identifiers.org/hco/13/GRCh38#35926090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55304768-A-C

http://identifiers.org/hco/13/GRCh38#35926604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55304210-C-A

35926694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55304131-T-G

35926748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55304077-A-G

35926832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55303997-G-T

35926904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55303949-G-T

http://identifiers.org/hco/13/GRCh38#35927059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55303824-A-C

35927059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55303824-A-T

35927177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55303713-C-G

35927395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55303510-G-C

35927412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55303493-G-A

35927694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55303179-C-T

http://identifiers.org/hco/13/GRCh38#35927846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#55302636-C-A

35927851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55302631-G-A

35927992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55302500-T-G

35928006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55302486-C-T

35928263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55302278-G-A

35928263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55302278-G-C

35928567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55302035-G-A

35928567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55302035-G-C

http://identifiers.org/hco/13/GRCh38#35929849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55301120-C-A

35930300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55300761-C-T

35930349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55300714-C-T

35930421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55300636-T-C

35931085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55299638-T-C

35931148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55299572-T-C

35931197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55299524-C-T

35931271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55299445-G-T

35931418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55299301-G-C

35931487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55299242-A-T

35931529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55299201-C-T

35931624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55299120-A-G

35931694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55299060-G-A

35932009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55298598-C-T

35932056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55298565-G-C

35932056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55298565-G-T

35932058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55298563-A-T

35932090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55298531-T-C

35932257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55298394-A-G

35932257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55298394-A-T

35934781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55298168-T-C

35934804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55298149-C-T

35934805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55298148-A-G

http://identifiers.org/hco/13/GRCh38#35934955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55298003-C-A

http://identifiers.org/hco/13/GRCh38#35935128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55297859-C-A

http://identifiers.org/hco/13/GRCh38#35935207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55297781-A-C

35935451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55297594-G-A

35935451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55297594-G-C

35935482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55297562-A-G

35935515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55297518-A-G

35935515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55297518-A-T

35935755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55297269-G-A

35936054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55296968-G-T

http://identifiers.org/hco/13/GRCh38#35936170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55296847-A-C

35936393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55296323-C-T

35936525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55296103-G-C

35936536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55296092-T-C

35936604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55296025-T-G

http://identifiers.org/hco/13/GRCh38#35936797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55295788-A-C

35937448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55295489-G-A

35937999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55295045-A-G

35938202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55294889-C-T

35938242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55294850-G-A

35939098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55294333-T-C

35939677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55293933-T-C

35939812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55293815-G-A

35940327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55293604-C-T

35941023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55292941-A-G

35941023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55292941-A-T

35941072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55292893-G-C

35941076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55292889-C-T

35941382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55292686-A-G

http://identifiers.org/hco/13/GRCh38#35941413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55292655-C-A

35941413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55292655-C-T

35941465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55292599-T-C

35941543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55292524-C-T

35943795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55291753-G-A

35943964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55291591-T-A

35944004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55291551-G-A

35944085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55291474-C-T

35944099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55291456-T-C

35944178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55291377-C-T

35944181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55291374-C-G

35944279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55291279-C-T

35944344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55291214-G-A

35944814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55290738-G-A

35945433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55290145-G-C

35945449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55290129-G-T

35945513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55290079-G-T

35945539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55290054-A-G

35945668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55289926-C-T

35945692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55289901-C-T

35945703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55289889-C-G

35945783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55289808-T-C

35946227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55289272-C-T

35946443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55289136-T-A

35946700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55288963-T-C

35946792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55288872-A-G

35946802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55288855-C-T

35947482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55288175-A-G

35947512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55288143-A-G

http://identifiers.org/hco/13/GRCh38#35947523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55288129-C-A

35947523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55288129-C-G

35947523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55288129-C-T

35947854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55287790-A-G

35948158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55287155-T-C

35949637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55286381-T-C

35949637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55286381-T-G

35949703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55286324-T-C

35950299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55285760-A-G

35951081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55285065-A-G

35951108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55285039-C-G

35951187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55284961-T-C

35951605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55284667-G-A

35951942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55284357-C-G

35952307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55283969-A-G

35952415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55283750-A-G

35952481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55283684-A-G

35952481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55283684-A-T

35952604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55283555-T-C

35952698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55283466-T-G

35952742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55283422-A-T

35952888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55283309-G-A

35953291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55281741-G-A

http://identifiers.org/hco/13/GRCh38#35954029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#55281015-C-A

35954035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55281009-A-T

35954172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55280859-T-C

35954301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55280674-T-C

35954327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55280648-G-A

35954346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55280629-G-A

35954347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55280628-T-C

35954377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55280600-C-G

35954377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55280600-C-T

35954537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55280464-T-G

35955397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55278372-G-C

35955403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55278366-C-T

35955944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55277709-G-T

35955951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55277702-G-A

http://identifiers.org/hco/13/GRCh38#35957105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55276802-A-C

35957132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55276775-G-T

35957297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55276611-T-C

35957671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55275891-C-T

35957701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55275861-A-G

35957977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55275555-G-A

35957986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55275546-A-G

35958007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55275525-A-G

http://identifiers.org/hco/13/GRCh38#35958018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#55275514-C-A

35958018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55275514-C-T

http://identifiers.org/hco/13/GRCh38#35958032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55275498-A-C

http://identifiers.org/hco/13/GRCh38#35958037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55275493-C-A

35958037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55275493-C-G

35958037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55275493-C-T

http://identifiers.org/hco/13/GRCh38#35958051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#55275479-C-A

35958051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55275479-C-T

35958064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55275466-T-A

35958064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55275466-T-C

35958078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55275452-C-G

35958078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55275452-C-T

http://identifiers.org/hco/13/GRCh38#35958086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55275444-A-C

35958091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55275439-C-T

http://identifiers.org/hco/13/GRCh38#35958136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55275346-A-C

35958142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55275340-C-T

35958144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55275338-C-T

35958151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55275331-C-G

35958151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55275331-C-T

35958152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55275330-A-G

35958176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55275306-A-G

http://identifiers.org/hco/13/GRCh38#35958196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#55275267-C-A

35958196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55275267-C-T

http://identifiers.org/hco/13/GRCh38#35958198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#55275265-C-A

35958198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55275265-C-T

http://identifiers.org/hco/13/GRCh38#35958222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55275239-C-A

35958222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55275239-C-T

35958230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55275231-A-T

35958270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55275190-T-C

35958340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55275117-C-T

35958526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55274918-G-T

35958539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55274905-T-C

http://identifiers.org/hco/13/GRCh38#35958544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55274900-C-A

35958606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55274809-G-A

35958672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55274734-T-C

35958801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55274351-A-G

35958834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55274299-G-A

35959449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55273405-C-T

35959687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55272695-T-C

35959998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55272392-T-C

35960283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55272177-C-T

35960366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55272096-A-G

35960849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55271918-T-C

35960892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55271878-T-G

35961151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55271655-C-T

35961590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55270832-C-T

35961595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55270827-G-C

http://identifiers.org/hco/13/GRCh38#35961615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55270805-C-A

35961642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55270778-T-C

35961925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55270518-T-C

35962060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55270385-A-T

35962127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55270316-A-G

35962218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55270267-C-T

35963215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55269126-T-C

35963412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55268912-G-A

35963459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55268867-C-T

35963984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55268707-G-T

35964033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55268661-T-C

35964251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55268469-T-G

35964437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55268256-G-C

http://identifiers.org/hco/13/GRCh38#35964507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55268189-A-C

35964507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55268189-A-G

35964639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55268059-T-G

http://identifiers.org/hco/13/GRCh38#35964724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55267980-C-A

http://identifiers.org/hco/13/GRCh38#35964749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55267955-C-A

http://identifiers.org/hco/13/GRCh38#35965354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55267567-C-A

35965354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55267567-C-T

http://identifiers.org/hco/13/GRCh38#35965378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55267547-A-C

35965378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55267547-A-G

35965477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55267446-T-C

http://identifiers.org/hco/13/GRCh38#35965561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55267364-C-A

35965598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55267331-T-A

35965632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55267298-G-C

35969426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55266262-A-G

35969518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55266172-T-C

35969846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55265874-C-G

35969846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55265874-C-T

35969937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55265773-A-T

35969992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55265721-G-A

35970249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55265498-G-A

35970804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55265153-C-T

35970880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55265050-T-C

35970912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55265019-G-A

35970912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55265019-G-T

35970943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55264992-C-T

35970975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55264960-C-T

35971832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55264606-G-A

35971933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55264523-T-C

35971933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55264523-T-G

35972031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55264441-A-G

35972099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55264370-G-A

35972161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55264293-C-T

35972171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55264283-C-T

35976899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55263804-C-G

35976998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55263711-T-C

http://identifiers.org/hco/13/GRCh38#35977025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55263692-A-C

35977839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55263153-G-A

35977839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55263153-G-C

35977839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55263153-G-T

35977895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55263085-G-A

35977912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55263069-G-A

35978047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55262950-A-G

http://identifiers.org/hco/13/GRCh38#35978549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55262548-C-A

35978549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55262548-C-G

35978549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55262548-C-T

35978598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55262494-A-G

35978791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55262291-G-A

35979238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55261907-C-T

35979858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55261403-G-A

35980082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55261210-A-G

35984345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55260020-T-A

35984492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55259848-G-A

35984783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55259610-C-G

35984954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55259405-T-C

35985085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55259276-C-T

35985243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55259125-C-T

35985403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55258959-A-G

35985691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55258718-C-G

35986161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55258119-A-G

35986232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55258058-T-A

35986232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55258058-T-G

http://identifiers.org/hco/13/GRCh38#35986313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55257976-A-C

35986346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55257931-T-C

35986523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55257723-T-C

35986767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55257529-A-T

35987899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55255910-C-T

http://identifiers.org/hco/13/GRCh38#35988285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55255676-C-A

35988504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55255463-C-T

35988935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55255028-C-T

35988936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55255027-G-A

35988990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55254970-G-C

35989007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55254953-G-C

35989016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55254944-C-T

35989155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55254811-A-G

35989911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55253824-T-G

35990003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55253750-A-T

35990006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55253747-C-T

http://identifiers.org/hco/13/GRCh38#35990018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55253735-C-A

35990018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55253735-C-T

35990392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55252885-T-A

35990474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55252809-T-G

35990512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55252793-T-C

35990692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55252628-C-T

35991758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55250471-A-G

35991838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55250399-G-C

35991863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55250376-A-G

35992180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55250065-C-T

35992212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55250027-T-C

35992265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55249974-G-A

35992382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55249866-T-C

35992444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55249808-T-C

35992545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55249723-T-C

http://identifiers.org/hco/13/GRCh38#35992626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55249667-C-A

35992666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55249630-A-G

35992678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55249618-T-A

35992783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55249534-T-C

35992815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55249513-A-G

35992852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55249476-A-G

35992874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55249454-A-G

35992896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55249428-T-C

http://identifiers.org/hco/13/GRCh38#35993285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55249089-C-A

35994014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55248130-T-C

35994023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55248121-T-C

35994106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55248039-T-A

35994180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55247967-T-C

35994205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55247942-G-A

http://identifiers.org/hco/13/GRCh38#35994206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#55247941-A-C

35994209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55247938-T-A

35994304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55247893-A-T

35994377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55247822-A-G

35994507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55247723-T-C

35994612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55247617-C-T

35994634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55247602-T-A

35994722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55247513-C-T

35994950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55247282-A-T

35995159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55247095-A-G

35995176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55247078-A-G

35995361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55246923-T-A

35995361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55246923-T-C

35995493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55246812-C-T

35995639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55246665-C-G

35995725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55246573-A-G

http://identifiers.org/hco/13/GRCh38#35996279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55246139-A-C

35996279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55246139-A-G

35996487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55245929-G-A

35996494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55245922-A-G

35996494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55245922-A-T

35996500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55245916-C-T

35996513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55245903-A-T

35996516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55245900-T-C

35996600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55245810-G-A

35996716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55245704-T-C

35997046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55245433-A-G

35997298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55245206-C-T

http://identifiers.org/hco/13/GRCh38#35997299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55245205-C-A

http://identifiers.org/hco/13/GRCh38#35997467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55245044-C-A

35997517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55244995-C-G

35997657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55244842-G-T

35998130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55244408-A-T

35998218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55244321-G-A

35999378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55243238-G-C

35999730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55242914-A-G

35999741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55242903-T-C

35999788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55242853-T-C

35999913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55242739-A-T

http://identifiers.org/hco/13/GRCh38#36000000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55242654-C-A

36000123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55242568-T-C

36000188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55242523-T-C

36000259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55242448-C-T

36000332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55242388-G-A

36000332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55242388-G-T

36000338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55242382-A-T

36000572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55241877-T-A

36000626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55241823-T-C

http://identifiers.org/hco/13/GRCh38#36000687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55241780-C-A

36000687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55241780-C-T

36001426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55241436-C-T

36001574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55241297-T-G

http://identifiers.org/hco/13/GRCh38#36001652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55241219-C-A

36002166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55240709-A-T

36002472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55240168-G-A

36002480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55240160-T-G

36002590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55240050-T-G

36002615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55240025-T-C

36003060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55239642-T-C

36003060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55239642-T-G

36003071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55239631-C-T

36003117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55239585-G-C

36003223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55239513-C-T

http://identifiers.org/hco/13/GRCh38#36005329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55237540-A-C

36005331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55237539-G-A

36005442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55237436-T-G

36005699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55237169-C-G

36005699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55237169-C-T

http://identifiers.org/hco/13/GRCh38#36006503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#55236445-C-A

36006503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55236445-C-T

36018386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55235696-C-G

36018386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55235696-C-T

36018584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55235504-C-T

36018682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55235405-T-C

36018758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55235331-C-G

36018854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55235235-A-T

http://identifiers.org/hco/13/GRCh38#36019131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55234975-C-A

36019148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55234958-T-C

36019158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55234948-T-C

36019536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55234575-T-C

36019702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55234420-G-T

36019705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55234417-T-G

36019848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55234263-A-G

36020557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55233725-C-G

36020723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55233615-A-G

http://identifiers.org/hco/13/GRCh38#36020950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55233354-A-C

36020950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55233354-A-G

36021215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55233121-T-C

36021220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55233116-C-G

36021220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55233116-C-T

36021273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55233064-G-A

36025771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55231834-C-T

36026066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55231484-C-T

http://identifiers.org/hco/13/GRCh38#36026372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55230871-C-A

36026439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55230804-T-G

36026471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55230772-C-T

36026632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55230630-T-C

36026650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55230613-G-A

36026800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55230466-A-G

36026800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55230466-A-T

36026920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55230343-T-C

36027093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55230180-T-C

36027664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55229966-A-G

36028002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55229695-T-C

36028036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55229667-C-T

36028090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55229644-G-T

36028228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55229502-G-A

36028228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55229502-G-T

36028293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55229438-A-G

36028388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55229336-C-G

36028463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55229256-T-A

36029310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55229045-G-A

36029374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55229031-C-T

36029404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55229014-T-G

36029456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55228961-A-G

36029465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55228952-C-T

36029731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55228678-A-G

36029902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55228499-G-A

36031886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55227248-C-T

36032741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55226678-G-A

36032778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55226642-T-G

36032841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55226579-T-C

36032863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55226557-T-C

http://identifiers.org/hco/13/GRCh38#36033029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55226413-C-A

36033363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55225830-T-C

36033383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55225809-A-T

36033438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55225756-G-A

36034047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55225442-A-G

36034092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55225393-C-G

36034092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55225393-C-T

36034107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55225374-G-T

36034209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55225253-A-G

36034432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55225066-C-T

36034546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55224982-G-C

36034709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55224829-A-G

36034719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55224819-C-T

36034774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55224764-C-T

36035002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55224570-C-T

36039028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55223769-T-G

36039039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55223757-C-T

36039133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55223665-A-T

36039206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55223594-C-T

36039675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55223114-T-A

36040047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55221204-G-C

36040170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55221122-T-C

36040223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55221062-A-G

36040716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55220604-T-C

36041053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55220272-C-T

36041295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55220004-C-T

36041398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55219913-T-C

36041406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55219905-T-C

36041437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55219876-A-G

36041480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55219833-C-T

36042005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55219328-T-C

36042112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55219221-G-C

36047664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55219019-A-G

36047664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55219019-A-T

36047715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55218966-A-T

36048219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55218447-T-C

36048466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55218201-T-C

36048595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55218072-C-T

36048979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55217706-T-C

36049042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55217658-T-G

36049308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55217199-T-A

36050316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55215644-A-G

36050448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55215542-A-G

36050559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55215400-T-C

36050582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55215377-C-T

36050583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55215376-A-T

36050615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55215344-T-C

36050746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55215214-C-T

36050893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55215070-C-G

http://identifiers.org/hco/13/GRCh38#36051077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55214912-A-C

http://identifiers.org/hco/13/GRCh38#36051155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55214842-A-C

36051308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55214698-A-G

http://identifiers.org/hco/13/GRCh38#36051482-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55214535-A-C

36051482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55214535-A-G

36051506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55214510-G-T

36051535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55214484-T-C

36051545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55214474-T-C

36051592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55214429-T-C

36051674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55214354-A-G

36051847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55214215-T-G

36051852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55214210-T-A

36053186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55213217-A-T

36053248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55213155-A-G

36053640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55212570-T-A

36054631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55208265-T-C

36054651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55208247-T-C

36054772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55208145-G-A

36054787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55208130-G-A

36054911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55208069-C-T

http://identifiers.org/hco/13/GRCh38#36055077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55207945-C-A

36055388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55207652-G-A

36055519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55207510-A-T

36055530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55207499-G-C

36055530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55207499-G-T

36055569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55207459-C-T

36055581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55207447-G-A

36055716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55207318-T-C

36059821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55206601-A-G

36059829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55206593-A-G

36059834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55206588-G-T

36060311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55206424-T-A

36060311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55206424-T-C

http://identifiers.org/hco/13/GRCh38#36060401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55206327-A-C

36060438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55206292-G-A

http://identifiers.org/hco/13/GRCh38#36060491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55206243-C-A

36060732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55205657-T-C

36060758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55205593-A-T

http://identifiers.org/hco/13/GRCh38#36060784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55205567-A-C

36060847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55205515-G-A

36060861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55205499-C-T

36060892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55205463-G-A

36060935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55205422-A-G

36061009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55205353-T-A

36061089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55205282-A-T

http://identifiers.org/hco/13/GRCh38#36061166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55205196-A-C

36061199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55205166-C-G

36061199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55205166-C-T

36061224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55205148-C-T

36061264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55205106-A-G

36061323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55205047-T-C

36061367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55205001-T-C

36061488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55204883-C-T

36061681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55204711-G-A

36061975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55204457-A-G

36062243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55204235-T-G

36062514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55203887-C-T

36062531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55203870-T-C

36062834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55203110-T-C

36062923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55203023-A-T

36062953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55202990-A-G

36062954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55202989-T-C

36063260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55202695-A-T

http://identifiers.org/hco/13/GRCh38#36063318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55202640-C-A

36063318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55202640-C-T

36063486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55202484-T-C

36063574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55202409-T-C

36063584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55202400-C-T

36063737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55202243-T-G

36063848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55202144-G-A

36063921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55202079-T-G

36067715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55200387-G-A

http://identifiers.org/hco/13/GRCh38#36067722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55200380-A-C

36067722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55200380-A-G

36067861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55200251-G-A

36067861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55200251-G-C

36067918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55200185-A-G

http://identifiers.org/hco/13/GRCh38#36068244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55199642-C-A

http://identifiers.org/hco/13/GRCh38#36068375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55199515-C-A

36068500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55199411-T-A

36068840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55198875-C-T

36069054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55198661-T-G

36069484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55198297-T-G

36069529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55198258-G-A

36069552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55198232-T-C

36069570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55198214-T-C

36069847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55197929-T-A

36069847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55197929-T-C

36070053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55196797-T-A

36070966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55196251-A-G

36071433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55195546-A-G

36071572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55195424-G-A

36071674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55195311-T-A

36071979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55194823-T-C

http://identifiers.org/hco/13/GRCh38#36072885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55193560-A-C

http://identifiers.org/hco/13/GRCh38#36073174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55193065-C-A

36073329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55192946-G-A

36073345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55192936-G-T

36073819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55192540-A-G

36073831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55192528-G-A

36073863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55192498-A-G

36074019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55192344-C-T

http://identifiers.org/hco/13/GRCh38#36074547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#55192082-C-A

36074547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, undefined
orthologous variants: 55192082-C-G

36074635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55191996-T-C

36074716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55191929-T-C

36074929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55191716-G-C

36075299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55191385-T-C

36080125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55190759-G-A

36080125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55190759-G-C

36080283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55190674-G-T

36080423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55190536-C-T

36080424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55190535-G-A

36080433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55190526-T-C

36080746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55190264-G-A

36080747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55190263-G-A

36080747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55190263-G-C

36080832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55190205-C-G

36081064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55190132-C-T

36081065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55190131-G-A

36081220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55189980-A-G

36081355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55189675-C-T

36081449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55189582-C-T

36081513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55189521-A-G

36082980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55187472-G-A

36083032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55187420-T-C

36083032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55187420-T-G

36083176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55187295-A-G

36083308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55187152-T-C

36083332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55187134-C-T

36083340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55187126-C-G

36083443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55186939-G-A

36083446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55186936-T-C

36083453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55186924-C-T

36084509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55185543-C-T

36084742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55185313-C-G

36084787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55185267-G-C

36093614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55184283-G-A

36093631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55184266-C-T

36093662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55184235-C-T

36093718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55184179-A-G

36096004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55181723-T-C

36096045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55181682-A-G

36096079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55181647-T-C

36096328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55181481-G-C

36096426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55181402-A-G

36096515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55181314-G-A

36096515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55181314-G-C

36096658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55181198-T-C

36097163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55180740-G-A

36097163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55180740-G-C

http://identifiers.org/hco/13/GRCh38#36097316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55179248-A-C

36097415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55179145-G-A

36097589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55178953-T-C

36097668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55178879-C-T

http://identifiers.org/hco/13/GRCh38#36097849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55178712-C-A

36097849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55178712-C-T

36097862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55178699-G-A

36097866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55178695-C-T

36098079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55178501-C-T

36098465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55177845-G-T

36098530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55177786-A-G

36098558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55177753-T-C

36099650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55176197-A-G

36099672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55176176-T-G

36099933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55175929-T-C

http://identifiers.org/hco/13/GRCh38#36099936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55175926-C-A

36099936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55175926-C-G

36099986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55175878-A-G

http://identifiers.org/hco/13/GRCh38#36100773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55175467-C-A

36100777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55175463-C-T

36101030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55175233-G-A

36101030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55175233-G-T

36101053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55175210-T-C

36101072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55175191-T-C

36103593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55174329-C-T

36103773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55174155-C-T

36103934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55174020-T-C

http://identifiers.org/hco/13/GRCh38#36104213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55173732-C-A

36104213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55173732-C-T

36104229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55173716-A-G

36104820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55172770-A-G

36106264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55170012-G-A

36106422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55169849-A-G

36106472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55169799-T-C

36106473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55169798-T-G

36107543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55168664-T-C

36107868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55168355-G-A

36107868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55168355-G-T

36108165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55168093-G-C

36108287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55168014-T-C

36108287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55168014-T-G

36108692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55167586-T-A

36108692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55167586-T-C

36108777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55167493-T-C

36108799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55167444-C-T

36108807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55167436-T-A

36108902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55166912-G-A

36109409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55166021-T-C

36109478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55165942-G-A

36109523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55165891-G-A

36109575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55165839-A-G

36109674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55165740-T-C

36109784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55165640-C-G

36109784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55165640-C-T

36109842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55165569-A-G

36109889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55165528-G-A

http://identifiers.org/hco/13/GRCh38#36109966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55165472-A-C

http://identifiers.org/hco/13/GRCh38#36110037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55165380-A-C

36110298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55164957-T-C

36110309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55164946-C-G

36110687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55164601-T-A

36111651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55163853-A-T

36111739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55163762-T-C

36111816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55163685-G-A

36111816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55163685-G-T

36111957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: missense variant
orthologous variants: 55163542-G-C

36112164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: missense variant
orthologous variants: 55163335-G-C

36112224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55163275-G-A

36112224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55163275-G-T

36112544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55162966-A-T

36112599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55162911-C-G

36112599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55162911-C-T

36112804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55162714-T-C

36113366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55162376-A-G

36113380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55162369-C-T

36113494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55162266-A-G

36118780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55160846-C-T

36118819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55160809-G-A

36119135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55160489-G-T

http://identifiers.org/hco/13/GRCh38#36119188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55160438-C-A

36119201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55160425-T-C

36119598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55160054-A-T

36119634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55160015-A-G

36119745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55159928-A-T

36119758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55159915-C-G

36119762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55159910-G-A

36119797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55159885-T-C

36120009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55159718-A-G

36120102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55159629-A-G

36120467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55159398-T-C

36120876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55159194-G-A

36120929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55159169-C-T

36121186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55158936-G-T

36121230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55158891-A-T

36122118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55158661-A-T

36122326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55158484-C-T

http://identifiers.org/hco/13/GRCh38#36122592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55158257-C-A

36123153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55157713-A-G

36123368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55157504-T-A

36123441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55157444-T-A

36123587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55156850-C-G

36123823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55156690-C-T

36124023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55156524-C-T

36124583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55155964-T-C

36124904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55155719-G-A

36125033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55155595-A-G

36125159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55155473-C-T

36125219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55155422-G-A

36125259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55155379-T-A

36125309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55155329-T-C

36125381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55155279-G-C

36125431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55155230-T-C

36125504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55155169-T-C

36125571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55155102-A-T

36125573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55155100-C-T

http://identifiers.org/hco/13/GRCh38#36125618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55155056-C-A

36126163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 55154543-G-A

36126163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 55154543-G-T

36126182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55154524-A-G

36126556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55154517-A-G

36126756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55154363-C-T

36126842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55154292-C-G

36127134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55154014-G-A

36127225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55153941-T-C

36127355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55153800-T-C

36127452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55153737-A-G

36127452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55153737-A-T

36127912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55153389-G-T

36128067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55153253-T-A

36128394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55152741-G-A

36128453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55152683-G-A

36128453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55152683-G-T

http://identifiers.org/hco/13/GRCh38#36128519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55152653-C-A

36128693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55152562-A-G

36128859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55152402-A-T

36128926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55152338-C-T

36129043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55152227-T-A

36129069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55152200-C-T

36129174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55152102-A-G

36129384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55151917-T-A

http://identifiers.org/hco/13/GRCh38#36129463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55151845-C-A

36129639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55151643-A-T

http://identifiers.org/hco/13/GRCh38#36129874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55151424-A-C

36130094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55151182-C-T

36130250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55151030-T-C

36130526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55150728-G-A

36130526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: 55150728-G-T

http://identifiers.org/hco/13/GRCh38#36130601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55150653-C-A

http://identifiers.org/hco/13/GRCh38#36131093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55150191-C-A

http://identifiers.org/hco/13/GRCh38#36131194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55150107-C-A

36131194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55150107-C-T

http://identifiers.org/hco/13/GRCh38#36131765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#55149592-C-A

36131773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 5 prime UTR variant
orthologous variants: 55149584-T-C

36131879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2700
most severe consequence: 5 prime UTR variant
orthologous variants: 55149489-A-G