78179276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24669938-G-A

78179317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24669974-G-T

78179343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24669998-G-A

78179343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24669998-G-T

78179384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24670027-G-T

78179694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24670262-A-G

78180027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24670561-G-T

78180204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24670710-A-G

78180395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24670916-C-T

78180557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24671061-G-A

78180743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24671241-A-G

78180764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24671259-T-C

78181539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24672169-A-G

http://identifiers.org/hco/10/GRCh38#78181702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24672321-C-A

78181711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24672330-A-G

78181724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24672339-A-T

78182079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24672500-G-A

78182238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24672665-C-T

78182269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24672696-G-T

78182440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24672821-C-T

78182552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24672937-G-A

78182586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24672971-G-T

78182885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24673265-G-A

78183021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24673376-G-A

78183021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24673376-G-C

78183021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24673376-G-T

78183134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24673482-G-C

78183330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24673692-G-A

78183436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24673797-A-G

78183455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24673809-A-G

78183884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674001-A-G

78184007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674061-A-G

78184046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674103-C-T

78184187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674207-G-A

78184205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674225-A-T

78184235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674252-C-T

78184515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674355-G-A

78184695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674516-C-T

78184796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674602-C-G

78184859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674665-C-G

78184968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674768-G-A

78184976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674776-G-A

78185102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674892-C-G

78185102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674892-C-T

78185135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24675023-C-T

http://identifiers.org/hco/10/GRCh38#78185138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24675026-A-C

78185158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24675046-A-G

78185254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24675128-C-T

78185318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24675215-A-G

78185394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24675288-C-T

http://identifiers.org/hco/10/GRCh38#78185739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24675576-C-A

78185739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24675576-C-G

78186445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24676112-C-T

78186941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24676681-G-A

78186941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24676681-G-T

78187063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24676778-A-T

78187162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24676862-A-G

78187206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24676914-A-T

78187286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24677084-T-C

78189683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24680070-A-G

78189711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24680102-A-G

78189793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24680163-G-A

78189977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24680312-G-T

78189978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24680313-G-A

78190253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24680580-G-A

78190846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24681370-C-T

78197202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24684011-G-A

78197287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24684102-T-C

78197509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24684348-C-T

78197546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24684503-G-A

78197615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24684562-C-T

78197834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24684733-A-G

78197887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24684775-A-G

78198195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24685045-G-A

78198284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24685135-T-G

78198318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24685163-C-T

78198482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24685224-C-T

78198489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24685231-G-A

78198497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24685239-A-G

78198784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24685440-C-T

78198795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24685451-G-A

78199138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24685786-T-G

http://identifiers.org/hco/10/GRCh38#78199239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24685875-C-A

78199239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24685875-C-T

78199260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24685896-A-G

78199276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24685912-G-T

78199369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24686006-A-G

78199540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24686175-G-A

78199670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24686305-T-C

78199953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24686545-G-T

78200159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24686743-A-G

78200247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24686831-G-A

78207221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24690927-C-G

78207221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24690927-C-T

78207250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24690956-T-C

78207437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24691139-G-A

78208005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24692045-A-T

78208214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24692233-C-T

78208663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24692673-A-G

78208799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24692843-C-G

78208921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24692970-G-A

78209174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24693222-T-G

78209254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24693300-C-T

78209904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24694151-G-A

78209904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24694151-G-C

78209904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24694151-G-T

78210058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24694277-T-C

78210300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24694506-T-A

78211080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24695938-C-T

78211091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24695949-T-C

78211124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24695975-G-T

78211150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24696000-C-T

78211547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24696377-G-A

78211601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24696431-G-T

78216160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24697280-A-G

http://identifiers.org/hco/10/GRCh38#78216170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24697290-A-C

78216207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24697318-A-G

78216267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24697379-G-T

http://identifiers.org/hco/10/GRCh38#78216543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24697641-C-A

http://identifiers.org/hco/10/GRCh38#78216896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24698768-A-C

78216918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24698790-A-T

78217171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24698996-G-T

78217286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24699081-C-T

78217289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24699084-C-T

78217290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24699085-G-A

http://identifiers.org/hco/10/GRCh38#78217520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24699304-C-A

78217520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24699304-C-T

78217530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24699314-C-T

78217539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24699315-T-G

78217611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24699381-G-C

78218183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24700220-G-A

78218800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24700804-C-T

78218882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24700873-G-A

http://identifiers.org/hco/10/GRCh38#78219029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24701019-C-A

78219029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24701019-C-T

http://identifiers.org/hco/10/GRCh38#78219088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24701078-A-C

http://identifiers.org/hco/10/GRCh38#78219094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24701084-C-A

78219094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24701084-C-T

78219143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24701133-A-G

78220193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24701464-T-G

78220238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24701493-G-A

78220245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24701500-A-G

78220393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24701642-G-A

78220444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24701691-G-A

78220660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24701852-C-T

http://identifiers.org/hco/10/GRCh38#78220679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24701871-C-A

78220812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24702109-G-C

http://identifiers.org/hco/10/GRCh38#78220819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24702116-A-C

http://identifiers.org/hco/10/GRCh38#78220977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24702264-C-A

78220977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24702264-C-T

78221135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24702404-G-A

78221233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24702458-C-G

78221361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24702559-A-G

78221415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24702606-G-A

78221441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24702632-C-T

78221525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24702760-A-G

78223378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24706406-T-A

78223900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24707776-G-A

http://identifiers.org/hco/10/GRCh38#78223945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24707821-A-C

78223945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24707821-A-G

78223946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24707822-T-C

78224187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708058-C-T

78224191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708062-C-G

78224378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708079-G-C

78224439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708139-G-A

78224474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708176-C-T

78224556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708258-C-G

78224695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708504-A-G

78224839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708639-T-C

78224884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708684-C-G

78225026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708816-C-T

78225710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24709434-T-C

78225769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24709492-C-T

78225782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24709506-C-T

78226099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24709824-C-T

78226276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24710001-C-G

78226735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24710413-A-G

78228555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24713763-G-A

78228701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24713891-C-G

78228767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24713962-A-G

78228799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24713991-C-G

78228799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24713991-C-T

http://identifiers.org/hco/10/GRCh38#78229054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24714201-A-C

78229232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24714328-A-G

78229258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24714354-C-T

78229585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24714675-C-T

78229646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24714736-C-T

78230535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24715561-C-T

78230563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24715597-A-G

http://identifiers.org/hco/10/GRCh38#78230621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24715652-C-A

78230994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -G-A

78231408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24716851-G-T

78231491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24716903-C-T

78231834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24717195-C-G

78231936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24717481-A-G

78232054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24717598-G-A

78232356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24718236-G-A

http://identifiers.org/hco/10/GRCh38#78232453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24718329-C-A

78232453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24718329-C-G

78232528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24718409-T-A

http://identifiers.org/hco/10/GRCh38#78232556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24718436-A-C

78232625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24718489-G-C

78232653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24718513-A-G

78232814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24718673-G-A

78232815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24718674-T-A

78233146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24718907-G-A

78233146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24718907-G-C

78233224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24718989-G-A

78233264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24719040-C-G

78233267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24719043-G-A

78233268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24719044-C-T

78233419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24719195-C-T

78233466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24719244-T-C

78233466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24719244-T-G

78233566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24719343-C-G

78234763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24722105-A-G

78234846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24722181-A-T

http://identifiers.org/hco/10/GRCh38#78234915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24722243-C-A

78234915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24722243-C-T

78235327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24722583-A-G

78235327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24722583-A-T

78235521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24722747-C-T

http://identifiers.org/hco/10/GRCh38#78235577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24722815-C-A

http://identifiers.org/hco/10/GRCh38#78235744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24722900-C-A

78235778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24722934-C-T

78236752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24723450-G-A

78236813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24723498-T-C

78237036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24723707-C-G

78237079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24723750-C-T

78237155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24723809-G-A

78237300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24723954-G-T

78237356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24724032-C-T

78237713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24724295-G-A

78237730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24724312-A-G

78237730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24724312-A-T

78238598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24724605-G-A

78238910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24724906-G-T

78238958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24724953-C-T

78244915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24728232-G-T

78244938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24728255-C-T

78244994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24728294-C-T

78245020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24728320-C-G

78245064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24728330-C-T

78245101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24728360-C-T

78245153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24728412-C-T

78245466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24729049-A-T

78245864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24729263-G-C

78245944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24729403-T-C

78246016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24729481-A-T

78247387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24730836-C-G

78247400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24730849-G-T

78247440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24730889-G-T

http://identifiers.org/hco/10/GRCh38#78247466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24730913-C-A

78247466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24730913-C-T

78247488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24730934-T-G

78247950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24731568-C-G

78247950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24731568-C-T

78248069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24731657-C-G

78248261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24731855-G-A

78248274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24731868-G-A

78248389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24731973-T-C

78248424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24731977-G-A

http://identifiers.org/hco/10/GRCh38#78248587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24732106-C-A

78248587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24732106-C-T

78248646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24732157-G-T

78248771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24732291-G-A

78248775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24732295-G-T

78248829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24732350-C-T

78248936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24732453-G-A

78248973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24732490-G-T

http://identifiers.org/hco/10/GRCh38#78249040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24732558-C-A

78249040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24732558-C-T

78249380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24732924-G-A

78249488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24733028-T-C

78249508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24733041-G-A

78249570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24733107-G-A

78249676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24733207-G-A

78250052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24733521-G-T

78250134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24733638-C-G

78250134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24733638-C-T

http://identifiers.org/hco/10/GRCh38#78250203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24733799-C-A

78250203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24733799-C-G

http://identifiers.org/hco/10/GRCh38#78250344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24733970-C-A

78250344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24733970-C-T

78250447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24734062-C-T

78250496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24734106-T-A

78250633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24734202-T-C

78250648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24734217-T-C

78250709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24734273-G-T

78250879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24734437-A-G

http://identifiers.org/hco/10/GRCh38#78250964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24734522-C-A

78251207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24734749-A-G

78251210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24734752-G-A

78251210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24734752-G-T

78251265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24734807-C-T

http://identifiers.org/hco/10/GRCh38#78251383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24734913-C-A

78251383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24734913-C-G

78251383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24734913-C-T

78251448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24734993-A-T

http://identifiers.org/hco/10/GRCh38#78251605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24735475-C-A

http://identifiers.org/hco/10/GRCh38#78251771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24735634-C-A

78251771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24735634-C-T

78251848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24735707-C-T

78251885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24735743-A-T

78251980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24735835-G-A

78251982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24735837-G-A

78251982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24735837-G-T

http://identifiers.org/hco/10/GRCh38#78251983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24735838-C-A

78251996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24735851-A-T

http://identifiers.org/hco/10/GRCh38#78252032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24735891-C-A

78252104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24735965-A-G

78252145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24736013-T-C

78252267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24736120-T-C

78252286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24736137-A-G

78252302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24736153-G-T

78252365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24736201-G-A

78252365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24736201-G-T

78252375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24736211-C-T

78252377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24736213-G-A

78252377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24736213-G-T

78252397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24736232-T-C

http://identifiers.org/hco/10/GRCh38#78252420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24736256-C-A

78252420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24736256-C-T

http://identifiers.org/hco/10/GRCh38#78252429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24736265-C-A

http://identifiers.org/hco/10/GRCh38#78252437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24736273-C-A

http://identifiers.org/hco/10/GRCh38#78252439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24736275-C-A

78252439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24736275-C-G

http://identifiers.org/hco/10/GRCh38#78252472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24736303-C-A

78252472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24736303-C-T

78252473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24736304-A-G

http://identifiers.org/hco/10/GRCh38#78252482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24736311-C-A

78252482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24736311-C-T

http://identifiers.org/hco/10/GRCh38#78252592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24736419-C-A

78252705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24736574-G-A

78252705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24736574-G-T

78252718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24736587-G-A

78252765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24736636-G-C

78252803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24736685-T-A

78252884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24736756-G-A

78252884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24736756-G-C

78252903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24736775-A-G

78252909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24736781-A-G

78253106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24736958-T-C

78253250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24739196-G-T

78253594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24739522-G-C

78253681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24739609-C-T

78253808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24739709-G-A

78253951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24739848-A-G

78253963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24739860-G-A

78253981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24739878-C-T

78254032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24739929-G-A

78254032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24739929-G-T

78254199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24740084-G-A

78254200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24740085-G-C

78254204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24740089-T-C

78254348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24740189-C-T

78254515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24740337-G-A

78254572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24740391-C-T

78254587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24740403-A-G

78254694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24740518-G-C

78254694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24740518-G-T

78254700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24740524-G-A

78254782-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24740591-A-T

78254806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24740614-A-G

78254807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24740615-C-G

78254862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24740669-G-A

78254862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24740669-G-C

78254880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24740687-C-T

78254910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24740718-C-T

78255094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24740909-G-A

78255402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24741144-C-T

http://identifiers.org/hco/10/GRCh38#78255672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24741883-A-C

78255672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24741883-A-T

78255736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24741937-C-T

78255832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24742014-C-T

78255847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24742032-A-G

78256229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24742363-C-G

78256229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24742363-C-T

http://identifiers.org/hco/10/GRCh38#78256289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#24742417-C-A

78256334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24742431-C-T

78256355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24742450-G-A

78256375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24742469-C-T

78256424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24742514-C-G

78256666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24742745-C-G

78256692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24742772-C-T

78256938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24743742-A-G

78257034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24743826-A-G

78257065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24743860-T-A

78257114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24743902-G-T

http://identifiers.org/hco/10/GRCh38#78257140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24743928-C-A

78257264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24744048-G-A

78257491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24744260-T-C

78257641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24744567-C-G

78257641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24744567-C-T

78257684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24744661-C-T

78257780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24744775-A-G

78259477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24745362-T-C

78259640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24745520-C-T

http://identifiers.org/hco/10/GRCh38#78259675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24745555-C-A

78259727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24745605-G-C

78260004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24745875-A-G

78260370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24746239-G-T

78260657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24746527-G-A

78260984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24747516-T-C

78261268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24747747-C-T

78261388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24747862-A-G

78261526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24747992-C-T

78261609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24748066-C-T

78262299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24748668-A-G

http://identifiers.org/hco/10/GRCh38#78262311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24748680-C-A

78262311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24748680-C-T

78262456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24749576-T-A

78262503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24749614-G-C

78262503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24749614-G-T

78262527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24749631-C-T

78262822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24749860-G-A

78263025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24750062-G-T

78263120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24750156-G-A

78263190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24750222-C-T

78263350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24750362-G-A

78263350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24750362-G-T

78267484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24750558-T-C

78267546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24750602-T-C

78267760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24750816-C-T

78269184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24752217-T-C

78269628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24752653-T-G

78269656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24752680-G-A

78269664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24752688-G-A

78269682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24752706-C-T

78269846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24752858-G-A

http://identifiers.org/hco/10/GRCh38#78269887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24752925-C-A

78269887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24752925-C-T

http://identifiers.org/hco/10/GRCh38#78269921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24753091-C-A

78269921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753091-C-G

78269921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753091-C-T

78269923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753093-T-C

http://identifiers.org/hco/10/GRCh38#78269930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24753107-C-A

78269930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753107-C-T

78269932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753109-A-G

78269938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753115-G-T

78269986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753181-T-A

78269986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753181-T-C

78269997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753191-T-A

78269997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753191-T-C

78270148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753322-C-T

http://identifiers.org/hco/10/GRCh38#78270171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24753347-C-A

http://identifiers.org/hco/10/GRCh38#78270248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24753433-C-A

78270324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753506-A-G

78270333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753515-T-C

78270351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753533-C-T

78270635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753755-T-C

http://identifiers.org/hco/10/GRCh38#78270645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24753765-A-C

78270676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753796-G-A

78270676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753796-G-T

http://identifiers.org/hco/10/GRCh38#78270702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24753821-C-A

78270702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753821-C-G

78270702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753821-C-T

78270782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753875-T-C

78270895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753984-A-G

78271095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24754141-G-A

78271112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24754156-A-G

78271121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24754165-G-A

78271124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24754167-C-G

http://identifiers.org/hco/10/GRCh38#78273121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24755812-C-A

78273121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24755812-C-G

78273121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24755812-C-T

78274101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24756800-T-G

78274172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24756864-A-T

78274443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24757126-C-G

78274711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24757323-A-G

78275172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24757721-G-T

78275678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24758207-A-G

http://identifiers.org/hco/10/GRCh38#78275875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24758338-C-A

78275875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24758338-C-T

78276136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24758566-G-A

78276223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24758654-G-A

78276361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24758912-T-C

78276368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24758919-T-G

78276376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24758927-T-C

78276376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24758927-T-G

78276392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24758942-C-G

78276392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24758942-C-T

78277194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24759138-G-T

78277337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24759266-C-G

78277873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24759790-A-T

78277963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24759877-G-A

78277963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24759877-G-T

http://identifiers.org/hco/10/GRCh38#78277977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#24759891-C-A

78278168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24760042-T-C

78278469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24760248-G-A

78278514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24760288-G-A

78278841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24760812-C-T

78278876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24760847-C-T

http://identifiers.org/hco/10/GRCh38#78279065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24761035-A-C

78279560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24761247-G-A

78279560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24761247-G-T

78279796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24761370-A-G

http://identifiers.org/hco/10/GRCh38#78279831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24761397-C-A

http://identifiers.org/hco/10/GRCh38#78279922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24761492-C-A

78279922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24761492-C-T

http://identifiers.org/hco/10/GRCh38#78280258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24761814-C-A

78280258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24761814-C-G

78280258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24761814-C-T

78280282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24761838-T-C

78280317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24761865-A-G

78280458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24761985-G-A

78280606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24762093-C-T

78280980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24762372-G-A

78281031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24762423-G-A

78281052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24762444-T-A

http://identifiers.org/hco/10/GRCh38#78284277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24763353-C-A

78284299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24763375-C-T

78284519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24763627-C-T

78284787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24763894-G-A

78284934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24764022-C-T

http://identifiers.org/hco/10/GRCh38#78285573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24764597-C-A

78285611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24764640-A-G

78285733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24764765-T-A

78285733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24764765-T-G

78285794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24764839-G-A

78286325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24765504-G-A

78286448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24765621-G-C

78286463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24765636-C-T

78286484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24765656-T-A

78286780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24765938-C-T

78286792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24765950-G-A

78287054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24766212-C-T

78287456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24766605-T-G

78287531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24766668-A-G

78291071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24768463-T-C

http://identifiers.org/hco/10/GRCh38#78291245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24768638-C-A

78292431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24769989-C-T

78292536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24770118-C-G

78292536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24770118-C-T

http://identifiers.org/hco/10/GRCh38#78292545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24770127-C-A

78292545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24770127-C-T

78292677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24770251-T-C

78292985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24770522-T-C

78293265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24770796-C-T

78293371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24770902-G-A

78293371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24770902-G-C

78293699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24771210-T-C

78293708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24771219-T-C

http://identifiers.org/hco/10/GRCh38#78293813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24771326-C-A

78293813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24771326-C-T

http://identifiers.org/hco/10/GRCh38#78293866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24771379-C-A

78293914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24771426-G-T

78293950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24771462-A-G

78293987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24771487-G-A

78293987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24771487-G-T

78294071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24771548-G-A

78294071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24771548-G-T

http://identifiers.org/hco/10/GRCh38#78294216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24771682-C-A

78294220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24771686-C-T

http://identifiers.org/hco/10/GRCh38#78294749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24771912-C-A

78294749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24771912-C-G

78294788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24771951-G-T

78294932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24772054-A-G

78295066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24772176-G-A

78295296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24772369-T-G

78295341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24772407-G-T

78295380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24772445-G-A

78295478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24772542-A-G

78295628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24772688-C-G

78295664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24772705-T-C

78295709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24772750-C-T

http://identifiers.org/hco/10/GRCh38#78295879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24772868-C-A

78296082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24773010-A-G

78296120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24773038-G-A

78296131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24773048-T-A

78300757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24775574-T-C

78300765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24775582-G-T

78300796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24775641-G-T

78300827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24775672-G-A

78300827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24775672-G-T

http://identifiers.org/hco/10/GRCh38#78301405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24776119-A-C

http://identifiers.org/hco/10/GRCh38#78301544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24776242-C-A

78301544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24776242-C-T

http://identifiers.org/hco/10/GRCh38#78301578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24776275-A-C

78301578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24776275-A-G

78301590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24776287-G-A

78301590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24776287-G-T

78301591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24776288-A-G

78301591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24776288-A-T

78301642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24776333-A-G

http://identifiers.org/hco/10/GRCh38#78301870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24778411-C-A

78301878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24778420-G-A

78301878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24778420-G-T

78302037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24778577-A-G

78302067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24778609-A-G

78302146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24778677-T-C

78302149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24778680-C-T

78302161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24778692-G-A

78302161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24778692-G-T

78302276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24778793-T-C

78302307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24778830-G-A

78302307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24778830-G-C

78302308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24778831-T-C

78302339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24778854-G-A

78302357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24778872-C-T

78302467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24778978-G-A

78303220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24779643-C-T

78303320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24779742-G-T

78303455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24779872-C-T

78303485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24779918-C-T

78303487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24779920-G-A

78303487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24779920-G-C

78303487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24779920-G-T

78303779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24780212-A-G

78304212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24780850-A-G

http://identifiers.org/hco/10/GRCh38#78304249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24780903-C-A

http://identifiers.org/hco/10/GRCh38#78304345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24781038-A-C

78304350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24781043-A-G

78304351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24781044-T-C

78304355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24781048-G-T

78304411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24781094-C-G

78304411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24781094-C-T

78304412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24781095-C-T

78304512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24781168-G-T

78304604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24781274-G-C

78304843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24781644-C-G

78305157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24781918-C-G

78306642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784206-G-A

78307634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785185-C-T

78307910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785697-C-T

78307964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785749-C-T

78307976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785759-G-A

78308060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785823-A-G

78308264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786050-T-A

78308264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786050-T-C

http://identifiers.org/hco/10/GRCh38#78308274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24786059-C-A

78308274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786059-C-T

78308686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786345-A-G

78308935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786818-A-G

78309080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786945-G-C

http://identifiers.org/hco/10/GRCh38#78309333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24787228-C-A

78309379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787276-G-C

78309536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787684-A-G

78309675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787811-C-T

78309676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787812-T-C

78309827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787932-G-A

78310015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24788109-T-G

78314855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24792061-G-A

78315102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24792284-A-G

http://identifiers.org/hco/10/GRCh38#78315318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24792521-C-A

78315823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24792940-T-C

78316432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24793990-G-C

78316727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24794266-C-G

78316727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24794266-C-T

78317008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24794506-G-A

78317137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24794616-G-A

78317137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24794616-G-T

78317292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24794702-A-G

78317295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24794705-G-A

78317295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24794705-G-T

78317300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24794710-T-G

78317436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24794854-C-T

78318039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24795392-C-G

78318039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24795392-C-T

78318218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24795595-T-A

78318218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24795595-T-C

78319048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796023-A-G

78319133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796111-G-A

78319341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798034-G-A

78319421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798110-A-G

78319504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798192-G-T

78319654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798332-C-T

78319704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798378-G-A

78319969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798631-A-T

78321625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800560-G-A

78321692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800632-G-T

78321759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800699-T-C

78321770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800710-G-A

78321854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800810-G-A

78321916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800859-A-T

78329931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24801224-G-A

78329962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24801258-G-A

http://identifiers.org/hco/10/GRCh38#78330155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24801429-C-A

http://identifiers.org/hco/10/GRCh38#78330240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24801512-A-C

78330240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24801512-A-G

78330254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24801526-G-A

http://identifiers.org/hco/10/GRCh38#78330265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24801537-C-A

78330265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24801537-C-T

78330280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24801555-A-T

78330281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24801556-G-T

http://identifiers.org/hco/10/GRCh38#78330315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24801588-C-A

78330315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24801588-C-G

http://identifiers.org/hco/10/GRCh38#78330420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24801683-C-A

78330477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24801734-A-G

78330592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24801845-G-A

78330632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24801894-G-T

78330633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24801895-C-T

http://identifiers.org/hco/10/GRCh38#78330907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24803004-C-A

78330907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24803004-C-T

http://identifiers.org/hco/10/GRCh38#78330915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24803012-C-A

78330915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24803012-C-T

78331065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24803131-A-G

78331091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24803157-G-A

78331114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24803178-T-C

78331269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24803323-T-C

78331284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24803338-T-G

http://identifiers.org/hco/10/GRCh38#78331290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24803344-A-C

78331388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24803427-T-A

78331388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24803427-T-C

78331411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24803447-T-C

78331542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24803541-G-A

78331547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24803547-C-T

78331984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24803960-A-G

78334359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24806200-G-A

78334359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24806200-G-T

78334389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24806230-T-C

78334522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24806347-C-G

78334522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24806347-C-T

78335019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24807079-G-T

78335501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24807483-A-G

http://identifiers.org/hco/10/GRCh38#78336057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24807942-A-C

78336083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24807970-G-A

78336336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24808161-G-A

78336336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24808161-G-T

78336337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24808162-C-T

78336426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24808249-C-T

78336439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24808262-C-T

http://identifiers.org/hco/10/GRCh38#78336468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24808291-C-A

78336468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24808291-C-G

78336599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24808429-T-G

78336657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24808484-T-G

78336757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24808531-G-A

78336757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24808531-G-T

http://identifiers.org/hco/10/GRCh38#78337042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24808797-C-A

78337130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24808891-G-T

78337266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24809034-C-T

78337393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24809154-C-G

78341195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24810903-C-T

78341359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24811072-T-A

78341359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24811072-T-C

78341488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24811224-G-A

78341682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24811418-G-A

78341833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24811547-C-T

78341864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24811578-G-C

78341977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24811680-G-C

78342318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24812037-C-G

78342338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24812085-G-A

78342370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24812116-G-A

78342376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24812122-G-C

78342455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24812209-G-C

78342595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24812318-C-T

http://identifiers.org/hco/10/GRCh38#78342644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24812369-C-A

78342844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24812540-G-T

78343027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24812712-G-A

http://identifiers.org/hco/10/GRCh38#78343356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24812936-C-A

78343356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24812936-C-G

78343373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24812954-G-T

78343490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24813068-A-T

78343677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24813234-A-G

78343854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24813395-G-C

http://identifiers.org/hco/10/GRCh38#78347823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24817973-A-C

78347945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24818096-G-T

78347974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24818125-C-T

78348096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24818178-C-T

78348162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24818236-G-A

78348464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24818538-G-A

http://identifiers.org/hco/10/GRCh38#78348541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24818610-C-A

78348952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24818999-G-T

78348971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24819016-C-T

http://identifiers.org/hco/10/GRCh38#78348986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24819039-C-A

http://identifiers.org/hco/10/GRCh38#78349300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24819434-C-A

78349364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24819494-C-T

78349492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24819585-A-G

78349545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24819646-G-A

78349603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24819691-G-A

78350074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24820207-C-T

78350092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24820227-C-T

http://identifiers.org/hco/10/GRCh38#78350179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24820563-C-A

78350213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24820595-G-C

78350521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24820855-G-T

78351004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24821311-G-T

78351150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24821450-G-A

78352961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24821890-T-C

78353255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24822145-T-A

78353255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24822145-T-C

78353280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24822164-C-T

78353340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24822236-T-G

http://identifiers.org/hco/10/GRCh38#78353458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24822357-C-A

78353458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24822357-C-T

78353484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24822383-G-T

78353752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24823294-C-T

78353805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24823343-G-A

78353906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24823441-T-C

78354137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24823675-C-G

78354240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24823783-T-C

78354317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24823860-T-C

78354322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24823865-C-T

78354732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24824313-A-T

http://identifiers.org/hco/10/GRCh38#78354906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24824471-A-C

78354991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24824562-T-C

78354991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24824562-T-G

78355177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24824750-G-A

78355233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24824851-C-T

78355758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24825437-C-G

78355821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24825518-A-G

http://identifiers.org/hco/10/GRCh38#78355883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24825578-C-A

78355890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24825585-A-G

78355926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24825621-G-T

78355989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24825705-G-A

78356180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24825887-C-T

78356202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24825909-G-A

78356337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24826163-G-A

78356440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24826273-G-A

78356867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24826716-G-A

78357000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24826851-G-A

78357037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24826889-C-T

78357094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24826943-C-T

78357996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24827857-G-A

http://identifiers.org/hco/10/GRCh38#78358119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24827986-A-C

78358184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24828050-T-C

78358630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24828429-T-C

78358951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24828728-T-A

http://identifiers.org/hco/10/GRCh38#78359103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24828879-A-C

78359151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24828927-G-A

78359163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24828935-G-A

78359185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24828957-G-A

78359203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24828967-G-A

78359203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24828967-G-T

78359266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24829031-T-C

78359301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24829066-G-A

78359451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24829212-A-G

78359451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24829212-A-T

78359483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24829238-G-T

http://identifiers.org/hco/10/GRCh38#78359521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24829288-C-A

78359555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24829359-G-A

78359560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24829374-G-A

78359572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24829387-C-T

78359772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24829623-G-A

http://identifiers.org/hco/10/GRCh38#78360150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24830002-C-A

78360485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24830320-G-C

78360579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24830416-G-A

http://identifiers.org/hco/10/GRCh38#78360742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24830570-C-A

78360742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24830570-C-T

78360912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24830735-C-T

78363282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24830949-G-A

78364804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24831372-C-T

78364876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24831438-G-A

78364878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24831440-C-T

http://identifiers.org/hco/10/GRCh38#78365049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24831538-C-A

http://identifiers.org/hco/10/GRCh38#78365260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24831647-C-A

78365408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24831778-T-C

78365634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24831989-A-G

http://identifiers.org/hco/10/GRCh38#78365699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24832053-C-A

78365880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24832230-T-C

78365880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24832230-T-G

78366013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24832394-G-T

78366072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24832467-C-T

78366107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24832502-C-G

78366623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24832938-A-G

78366880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24833158-T-G

78367009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24833277-A-G

78367018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24833286-A-G

78367029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24833298-C-T

78367498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24833712-A-G

http://identifiers.org/hco/10/GRCh38#78368357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24834204-C-A

78368401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24834842-C-T

78368431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24834868-A-G

78368529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24834943-C-T

78368601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24835007-C-G

78368699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24835102-A-G

78368702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24835105-A-G

78368872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24835655-G-T

78368913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24835695-G-A

78368922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24835704-T-C

78368960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24835740-G-A

78368960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24835740-G-C

78368965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24835745-T-C

78369167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24835905-T-A

78369167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24835905-T-G

http://identifiers.org/hco/10/GRCh38#78369173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24835911-A-C

78369289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24836019-T-A

78369366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24836092-G-A

78369379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24836104-G-C

78369413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24836138-T-C

78369430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24836169-C-T

http://identifiers.org/hco/10/GRCh38#78369465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24836204-C-A

78369513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24836234-G-T

78369757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24836273-T-A

78369769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24836285-G-A

78370201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24837094-T-A

http://identifiers.org/hco/10/GRCh38#78370225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24837119-C-A

78370225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24837119-C-T

78370245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24837139-C-T

78370757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24837550-G-A

http://identifiers.org/hco/10/GRCh38#78370927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24837659-C-A

78370927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24837659-C-G

78371383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24837992-G-A

78371990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24838586-C-G

78372452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24839028-C-T

78372491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24839065-G-A

78372921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24839434-G-A

78372964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24839475-G-A

78373008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24839522-G-A

78373015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24839529-C-T

78373052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24839555-C-T

78373270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24839737-G-A

78373442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24839844-A-G

78373834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24840183-C-T

78374135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24840492-G-T

78374282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24840742-T-G

78374359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24840805-G-T

78374563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24841023-C-T

78375266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24841741-T-G

78375663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24842128-G-A

78376026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24842502-C-G

78376026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24842502-C-T

78376201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24842677-C-T

78376298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24842771-G-T

78376638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843079-T-G

78376642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843089-G-A

78376743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843189-G-C

78377047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843441-T-C

78377106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843500-C-T

78377137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843531-G-A

78377160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843554-A-G

78377179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843577-G-A

78378048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843906-G-A

78378075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843932-T-C

78378318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24844161-C-T

78378319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24844162-C-T

78378444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24844292-A-T

78378502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24844344-A-G

78378688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24844535-G-A

78378688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24844535-G-T

78379176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24844982-G-C

78379176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24844982-G-T

78379179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24844985-C-G

78379482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24845227-T-C

78379585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24845340-A-T

78379739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24845498-T-C

78380145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24845712-G-A

78380145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24845712-G-T

78380146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24845713-G-C

78380305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24845855-G-A

78380305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24845855-G-T

78380343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24845893-A-G

http://identifiers.org/hco/10/GRCh38#78380361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24845912-C-A

78380361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24845912-C-T

78380471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24845984-G-T

78380696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24846236-G-T

78380923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24846462-T-C

78380934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24846473-T-A

78380960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24846498-C-T

http://identifiers.org/hco/10/GRCh38#78381631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24847193-C-A

78381631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24847193-C-T

78381914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24847483-G-A

78382090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24847661-G-A

78382127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24847727-C-T

78382841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24848945-C-T

78382916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24849002-G-A

78383133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24849238-T-C

http://identifiers.org/hco/10/GRCh38#78383173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24849310-C-A

78383173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24849310-C-G

http://identifiers.org/hco/10/GRCh38#78383464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24849677-C-A

78383603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24849815-T-A

78388021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24851635-T-C

78388032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24851644-C-T

78388259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24851847-G-A

78388279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24851867-G-A

78388401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24852003-T-C

78388438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24852033-C-T

78388914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24852455-C-T

78391100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24854524-C-G

78391100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24854524-C-T

78391674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24855067-G-A

78391674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24855067-G-T

78391676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24855069-C-T

78391683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24855076-A-G

78391705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24855091-G-C

78392073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24855270-T-G

http://identifiers.org/hco/10/GRCh38#78392505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24855538-C-A

78392611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24855640-C-T

78392639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24855661-C-G

78392639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24855661-C-T

78392670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24855685-G-A

78392672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24855687-G-A

78392730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24855753-G-T

78392837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24855831-G-T

78392880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24855873-A-G

78393003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24855998-G-A

78393025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24856018-G-A

78393025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24856018-G-C

http://identifiers.org/hco/10/GRCh38#78393111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24856096-C-A

78393139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24856122-T-C

78393139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24856122-T-G

78393320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24856265-G-A

78393378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24856286-G-T

78393382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24856290-C-T

78393925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24856886-T-C

78394243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24857152-C-T

78394246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24857155-G-A

78394439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24857301-A-G

78394439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24857301-A-T

78394771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24857573-C-G

http://identifiers.org/hco/10/GRCh38#78394889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24857670-C-A

http://identifiers.org/hco/10/GRCh38#78394891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24857672-A-C

78394891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24857672-A-T

78394895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24857676-T-G

78394949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24857730-A-G

78394949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24857730-A-T

78401677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24860104-G-A

http://identifiers.org/hco/10/GRCh38#78401698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24860117-C-A

78401893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24860288-G-A

78402021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24860414-T-G

78402069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24860456-C-T

78402070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24860457-C-T

78402135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24860512-C-T

78402140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24860517-C-T

78402245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24860608-C-T

http://identifiers.org/hco/10/GRCh38#78402319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24860690-C-A

78402319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24860690-C-G

78405188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24863225-G-A

78405531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24863418-T-C

http://identifiers.org/hco/10/GRCh38#78405702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24863509-A-C

78405767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24863561-C-G

78405862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24863680-G-C

78405874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24863692-G-C

78406053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24863886-T-C

78406053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24863886-T-G

78406106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24863939-G-A

78406215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24864049-G-A

78406259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24864091-C-T

78406493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24864272-T-G

http://identifiers.org/hco/10/GRCh38#78406545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24864304-C-A

78406545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24864304-C-T

78406570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24864329-T-C

78406628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24864388-A-G

78406916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24864694-G-A

78406916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24864694-G-C

78407103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24864889-C-T

78407107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24864893-C-T

78407297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24864981-G-C

78407389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24865077-G-A

78407638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24865269-T-C

78407644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24865275-C-T

78407653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24865284-G-A

78407689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24865320-G-T

http://identifiers.org/hco/10/GRCh38#78407729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24865359-A-C

78407729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24865359-A-G

78407778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24865407-G-T

78408147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24865546-A-G

78408222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24865618-T-G

78408312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24865738-C-T

78408329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24865755-G-A

78408546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24865981-C-T

78408910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24866328-C-T

78408955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24866374-C-T

78409920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24866836-G-C

78409920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24866836-G-T

78409988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24866899-G-T

78410083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867000-C-T

78410168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867080-C-G

78410175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867085-C-G

78410175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867085-C-T

78410267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867176-C-T

78410309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867218-T-A

http://identifiers.org/hco/10/GRCh38#78410314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24867222-C-A

78410346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867250-C-G

http://identifiers.org/hco/10/GRCh38#78410417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24867314-A-C

78410502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867401-T-A

78410502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867401-T-C

78410502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867401-T-G

78410525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867424-G-C

78410565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867452-C-G

http://identifiers.org/hco/10/GRCh38#78410597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24867484-A-C

78410597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867484-A-T

http://identifiers.org/hco/10/GRCh38#78410626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24867516-C-A

http://identifiers.org/hco/10/GRCh38#78410755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24867663-C-A

78410755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867663-C-T

78410761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867669-C-T

78411077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24868300-T-G

78411121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24868330-G-A

78412619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24868574-G-A

78412862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24869122-G-A

78413018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24869271-G-A

78413025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24869277-C-G

78413255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24869499-A-G

78413421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24869652-C-T

78413541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24869765-C-T

78416183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24870213-T-C

78416241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24870267-T-C

http://identifiers.org/hco/10/GRCh38#78416633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24870623-A-C

78416905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24870899-A-T

78416957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24870951-T-C

78417424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24871388-G-A

78417812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24871801-C-T

78417813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24871802-G-A

78418004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24871990-C-G

78418004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24871990-C-T

http://identifiers.org/hco/10/GRCh38#78418056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24872042-C-A

78418073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24872060-G-A

78418111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24872099-G-A

http://identifiers.org/hco/10/GRCh38#78418128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24872116-C-A

78418229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24872245-C-T

78418235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24872251-G-A

78418254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24872270-C-T

78418644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24872604-G-T

78419502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24872848-G-C

78420021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24874071-G-A

78420104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24874157-G-T

78420158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24874233-A-T

78420338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24874400-T-C

78420630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24874866-T-C

78420632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24874868-T-C

78420703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24874958-C-T

78420778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24875026-T-A

http://identifiers.org/hco/10/GRCh38#78421180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24875349-C-A

78421180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24875349-C-T

78421214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24875383-G-A

http://identifiers.org/hco/10/GRCh38#78421294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24875476-C-A

78421294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24875476-C-T

78421295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24875477-G-A

78421295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24875477-G-C

http://identifiers.org/hco/10/GRCh38#78421361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24875544-A-C

78421361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24875544-A-G

78421659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24875843-C-T

78421735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24875919-T-C

78421861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24876033-T-G

78421883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24876064-C-G

78422204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24876425-C-T

78422283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24876503-C-G

78422524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24876708-G-C

78422551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24876735-A-G

78422990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24876905-A-G

78432478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24889429-C-T

78432631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24889557-T-C

78432771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24889667-A-G

http://identifiers.org/hco/10/GRCh38#78432780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24889676-C-A

78432781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24889677-A-G

78432883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24889797-A-T

78432920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24889956-C-T

78432945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24889981-G-A

78433053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24890071-G-A

78433094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24890108-C-T

78433098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24890112-C-T

78433122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24890136-C-T

78433272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24890237-C-T

78433306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24890262-A-G

78433444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24890337-C-T

78433691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24890428-A-G

78433721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24890459-C-T

78433795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24890547-C-T

http://identifiers.org/hco/10/GRCh38#78434303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#24891359-A-C

78434322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24891378-G-C

78434464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24891513-G-C

78435399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24895101-C-T

78435458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24895160-T-C

78435471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24895173-G-T

78435509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24895213-C-T

78435648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24895354-C-T

78435729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24895421-T-C

78435995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24895693-G-A

78436004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24895705-G-T

78436042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24895743-G-A

78436211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24895894-G-A

78439294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24896658-G-A

78439327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24896695-G-A

78439360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24896727-G-A

78439434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24896781-G-A

78439530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24896843-G-A

78439670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24896996-T-G

78440607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24899516-G-A

78440607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24899516-G-C

78441951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24900704-G-A

78441951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24900704-G-C

78442066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24900802-C-T

78442090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24900813-A-G

http://identifiers.org/hco/10/GRCh38#78442934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24901329-C-A

78442934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24901329-C-T

78443155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24901497-C-T

78443649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24901776-T-A

78443649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24901776-T-G

78444151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24902250-A-G

78444174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24902273-C-G

78444174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24902273-C-T

http://identifiers.org/hco/10/GRCh38#78444679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24902778-C-A

78444892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24902966-A-T

http://identifiers.org/hco/10/GRCh38#78445289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24903185-C-A

78445357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24903260-T-C

http://identifiers.org/hco/10/GRCh38#78445371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24903288-C-A

78445506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24903418-G-A

http://identifiers.org/hco/10/GRCh38#78445751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24903643-C-A

78445770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24903662-G-T

78446086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24903979-G-A

http://identifiers.org/hco/10/GRCh38#78446656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24904633-C-A

78446656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24904633-C-G

78446995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24904931-T-C

78447922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24905935-A-T

78447931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24905944-T-A

78447931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24905944-T-G

78448133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24906139-G-T

78448144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24906150-A-G

78448165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24906171-C-T

78448173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24906179-T-C

78448275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24906348-C-T

78448276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24906349-G-A

78448355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24906424-T-C

78448702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24906888-A-G

78448856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24907047-T-C

78448915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24907091-A-G

78448915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24907091-A-T

78448923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24907099-T-C

78448923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24907099-T-G

78448967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24907120-A-G

78450832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24908285-G-A

http://identifiers.org/hco/10/GRCh38#78451164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24908525-C-A

78451177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24908538-G-C

78451359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24908712-G-A

78451362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24908714-C-T

78451759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24909062-G-A

78451759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24909062-G-C

78451878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24909176-G-T

78452052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24909291-C-T

78453171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24909852-C-T

78453476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24910160-G-A

78453910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24910495-C-T

78453960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24910538-T-G

78453967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24910544-G-A

78453967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24910544-G-T

78454127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24910668-G-A

78454282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24910816-G-A

78454500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24911010-G-A

78454500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24911010-G-C

http://identifiers.org/hco/10/GRCh38#78454525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24911028-C-A

78454764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24911269-A-T

78454817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24911455-C-G

78454817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24911455-C-T

78455876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24912745-G-C

78456130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24912973-G-A

78456832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24913361-T-C

78457310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24913772-T-G

78457403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24913842-C-T

78457429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24913868-A-G

78457455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24913894-A-G

78457460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24913899-C-T

78457507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24913920-A-T

78457759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24914170-C-T

78457911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24914294-G-C

78458112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24914476-C-G

78458186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24914551-T-G

78458359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24914711-A-G

http://identifiers.org/hco/10/GRCh38#78458371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#24914722-C-A

78458469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24914817-A-G

http://identifiers.org/hco/10/GRCh38#78458912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -C-A

78458912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -C-T

78460458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24916715-C-T

78461412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24917658-T-C

78461425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24917671-G-A

78461473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24917718-T-C

78461751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24918369-C-T

78461925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24918559-C-T

78462154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24918828-A-G

78462442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24919072-G-A

78462523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24919169-G-A

78462554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24919199-C-T

78463484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24919840-T-C

78463850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24920071-C-T

78463911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24920130-G-A

78463985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24920172-G-A

78463993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24920180-A-G

78464030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24920208-C-T