120464374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5 prime UTR variant
orthologous variants: 51250888-C-T

120464388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5 prime UTR variant
orthologous variants: 51250902-G-A

120464388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5 prime UTR variant
orthologous variants: 51250902-G-C

http://identifiers.org/hco/5/GRCh38#120464407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51250921-C-A

http://identifiers.org/hco/5/GRCh38#120464430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51250944-C-A

120464430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5 prime UTR variant
orthologous variants: 51250944-C-T

120464482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5 prime UTR variant
orthologous variants: 51250998-A-T

120464600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 51251116-A-G

120464600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 51251116-A-T

120464653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 51251169-G-A

120464711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51251229-T-C

http://identifiers.org/hco/5/GRCh38#120464727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51251245-C-A

120464727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51251245-C-T

120464729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51251247-A-G

120464755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51251271-A-T

120464768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51251284-G-A

120464774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51251290-G-A

120464774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51251290-G-C

120464774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51251290-G-T

120464879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51251396-G-C

120465052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51251573-C-G

120465093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51251612-G-A

120465093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51251612-G-C

120465102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51251621-G-A

120465312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51251845-C-T

120465393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51251935-G-A

120465478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51252027-G-A

120465487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51252038-C-T

120465495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51252046-G-A

120465495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51252046-G-C

120465495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51252046-G-T

120465546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51252091-A-G

120465546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51252091-A-T

120465552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51252097-G-T

120465594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51252145-G-A

120465594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51252145-G-T

120465615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51252166-T-C

120465627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51252176-G-T

120465720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51252265-G-A

120465720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51252265-G-T

120465741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51252287-G-T

120465919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51252460-A-G

120466533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51253071-C-T

120466534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51253072-A-G

120466598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51253149-T-C

http://identifiers.org/hco/5/GRCh38#120466602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51253153-C-A

120466699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51253246-A-T

120467078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51253625-C-T

120467243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51253823-T-C

120467640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51254429-T-G

http://identifiers.org/hco/5/GRCh38#120467745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51254529-A-C

120468043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51254801-A-G

120468158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51254914-C-T

120468571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51255292-T-C

120468622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51255340-C-G

http://identifiers.org/hco/5/GRCh38#120468980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51255653-A-C

120469103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51255772-T-C

120469186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51255860-G-T

120470155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51256757-T-G

120470532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51257122-G-A

120470538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51257128-A-G

120470640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51257218-T-G

120470688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51257267-T-G

120470706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51257285-T-A

http://identifiers.org/hco/5/GRCh38#120471275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51257906-A-C

120471464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51258237-A-T

120471548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51258324-T-C

120471549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51258325-G-A

120471574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51258350-C-T

120471615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51258446-C-T

http://identifiers.org/hco/5/GRCh38#120471676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51258515-C-A

120471862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51258700-A-G

http://identifiers.org/hco/5/GRCh38#120471878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51258716-A-C

120471878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51258716-A-G

120472003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51258853-G-A

120472054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51258903-C-G

120472058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51258907-T-G

120472224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51259076-C-G

120472459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51259307-G-A

120472820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51260147-A-G

120472887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51260213-A-G

120473034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51260358-A-T

120473035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51260359-T-C

120473076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51260399-A-T

120473112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51260435-C-T

120478192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51263665-G-A

120478574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51264005-T-C

120478582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51264013-A-G

120479117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51264525-A-G

120479117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51264525-A-T

120479149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51264554-T-A

120479149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51264554-T-C

120479281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51264672-G-A

120479283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51264674-T-C

120479309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51264702-A-G

120479469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51264829-A-G

120479540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51264902-A-G

120479630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51264989-C-T

120479658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51265012-A-T

120479741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51265085-G-T

120479834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51265172-C-G

120479834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51265172-C-T

http://identifiers.org/hco/5/GRCh38#120479986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51265751-A-C

120480216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51265899-A-G

http://identifiers.org/hco/5/GRCh38#120480307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51265972-A-C

http://identifiers.org/hco/5/GRCh38#120480338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51265997-C-A

120480338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51265997-C-T

120480408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51266055-A-G

120480436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51266076-G-A

http://identifiers.org/hco/5/GRCh38#120480579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51266215-C-A

120480670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51266318-A-G

120480773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51266360-T-C

http://identifiers.org/hco/5/GRCh38#120481229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51266594-C-A

120481229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, missense_variant
orthologous variants: 51266594-C-G

120481229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, missense_variant
orthologous variants: 51266594-C-T

http://identifiers.org/hco/5/GRCh38#120481420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51266778-C-A

120481420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51266778-C-T

120481590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51266952-A-T

120481591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51266953-T-C

120481929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51267311-T-C

http://identifiers.org/hco/5/GRCh38#120483070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51268339-A-C

120483100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51268371-T-A

120483117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51268388-G-A

120483258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51268508-C-T

120483270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51268522-G-C

120483347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51268821-T-C

120483364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51268837-G-A

120483371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51268844-C-T

120483702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51269424-T-C

120484788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51270065-G-A

http://identifiers.org/hco/5/GRCh38#120484877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51270157-A-C

120484886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51270166-C-T

120485125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51270325-T-A

120485125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51270325-T-G

120485150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51270343-C-T

http://identifiers.org/hco/5/GRCh38#120485250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51270424-A-C

http://identifiers.org/hco/5/GRCh38#120485544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51270731-A-C

120485544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51270731-A-G

120485668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51270829-C-T

120501406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51277060-A-G

120502002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51277367-A-G

120502008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51277373-T-A

120502059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51277424-T-G

120502092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51277459-G-A

120502165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51277531-A-T

120502458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51278182-G-T

120502521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51278240-T-G

120502571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51278287-A-G

120502626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51278341-G-A

120502740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51278441-G-A

120502767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51278468-C-G

120502986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51278677-T-C

120502992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51278683-T-C

120503106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51278783-T-G

120503124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51278801-G-A

120503213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51278853-G-A

120503215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51278855-G-A

http://identifiers.org/hco/5/GRCh38#120503288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51278930-C-A

120503564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51279171-T-C

http://identifiers.org/hco/5/GRCh38#120503626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51279237-C-A

120504314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51279388-C-T

120504448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51279508-G-C

120504448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51279508-G-T

http://identifiers.org/hco/5/GRCh38#120504468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51279522-C-A

120504607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51279679-T-C

120504746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51279817-C-T

http://identifiers.org/hco/5/GRCh38#120504858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51279927-C-A

120504858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51279927-C-T

120504990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51280043-C-T

120504996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51280051-T-G

http://identifiers.org/hco/5/GRCh38#120505082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51280149-A-C

120505144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51280211-C-G

120505144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51280211-C-T

120505154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51280221-A-G

120507448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51282691-T-C

120507591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51282843-G-C

120507911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51283694-T-G

http://identifiers.org/hco/5/GRCh38#120507912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51283695-A-C

http://identifiers.org/hco/5/GRCh38#120507940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51283711-C-A

120507940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51283711-C-T

http://identifiers.org/hco/5/GRCh38#120508014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51283768-A-C

120508014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51283768-A-G

120508028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51283781-C-T

120508108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51283864-T-C

120508131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51283882-C-T

120508132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51283883-A-G

120508343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51284090-C-G

120508343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51284090-C-T

120508651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51284702-C-T

120508789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51284840-G-A

120509028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51285028-A-G

120509134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51285132-G-A

120509134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51285132-G-T

120509136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51285134-A-T

120509459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51285457-C-T

120509515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51285516-C-T

120509790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51285831-C-T

120509824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51286007-C-T

120509918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51286233-A-G

120510071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51286383-C-T

120510201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51286513-G-A

120510308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51286614-C-T

120510518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51286828-A-G

120510728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51287036-A-G

120510728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51287036-A-T

120510749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51287057-A-G

120510778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51287077-A-G

120510841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51287142-A-G

120510862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51287164-C-T

120510962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51287270-A-T

120510966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51287274-T-C

120511046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51287352-G-A

120511069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51287375-A-G

120511100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51287410-T-C

120511179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51287497-A-T

120511241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51287557-A-G

120511384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51287685-T-C

http://identifiers.org/hco/5/GRCh38#120511453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51287754-A-C

120511581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51287887-G-A

120511612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51287918-A-G

http://identifiers.org/hco/5/GRCh38#120511815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51288169-A-C

120511893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51288360-C-T

http://identifiers.org/hco/5/GRCh38#120511993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#51288447-A-C

120512070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51288527-G-C

120512133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51288587-A-G

120512182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51288659-C-T

http://identifiers.org/hco/5/GRCh38#120512356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51288822-C-A

120512376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51288843-A-G

http://identifiers.org/hco/5/GRCh38#120512458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51288924-C-A

120512458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51288924-C-G

http://identifiers.org/hco/5/GRCh38#120512552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51289054-C-A

120515550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51290081-T-A

120515624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51290145-C-T

120515673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51290186-G-C

120515721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51290227-T-A

120515721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51290227-T-C

120516735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51291697-T-C

http://identifiers.org/hco/5/GRCh38#120516794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51291756-A-C

120516868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51291831-A-G

120517171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51292142-A-G

http://identifiers.org/hco/5/GRCh38#120517490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51292428-A-C

120517522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51292489-A-G

120517617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51292580-T-G

120517829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51292786-G-T

120517924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51292876-A-T

http://identifiers.org/hco/5/GRCh38#120518000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51292951-A-C

120518000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51292951-A-G

120518050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51293001-C-G

120518542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51293936-G-A

http://identifiers.org/hco/5/GRCh38#120518553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51293947-C-A

120518667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51294059-T-C

120518668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51294060-C-T

120519127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51294341-T-C

120519575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51294710-C-T

120519650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51294782-T-C

120519941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51295065-A-G

120519941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51295065-A-T

120519965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51295100-C-T

120523629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51296021-A-G

120523656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51296043-A-G

120523656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51296043-A-T

120523773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51296209-G-A

120523841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51296303-G-A

http://identifiers.org/hco/5/GRCh38#120523868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51296332-C-A

120523885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51296349-A-G

http://identifiers.org/hco/5/GRCh38#120525207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51296431-C-A

120525207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51296431-C-T

120525219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51296443-T-C

120525246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51296470-A-G

120525282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51296503-T-C

120525486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51296645-A-G

120525535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51296695-C-T

120525642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51296790-G-A

http://identifiers.org/hco/5/GRCh38#120525645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51296793-A-C

120525741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51296874-A-T

120525813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51296915-G-C

120525862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51296967-A-G

120526012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51297110-G-C

120526087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51297187-C-T

120526102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51297202-G-T

120526286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51297355-G-T

120526325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51297380-A-G

http://identifiers.org/hco/5/GRCh38#120526350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51297392-C-A

120526350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51297392-C-G

120526363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51297408-G-A

120526571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51297573-A-G

120526600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51297603-T-G

120526673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51297681-T-A

120527227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51299540-A-T

120527242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51299555-G-A

120527251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51299564-T-G

120527323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51299654-T-C

120527417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51299738-G-T

http://identifiers.org/hco/5/GRCh38#120527437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51299758-A-C

120527539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51299835-C-T

120527643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51299915-G-A

120527799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51300060-G-T

120527807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51300068-A-G

120527808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51300069-C-T

120527887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51300143-A-G

120527906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51300162-G-A

120528055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51300303-G-A

120528136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51300384-G-A

120528136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51300384-G-T

120528140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51300388-G-A

http://identifiers.org/hco/5/GRCh38#120528246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51300768-C-A

http://identifiers.org/hco/5/GRCh38#120528299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51300832-A-C

120528413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51300939-T-C

120528414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51300940-A-G

120528465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51300990-G-T

120528704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51301196-C-T

http://identifiers.org/hco/5/GRCh38#120528708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#51301200-C-A

120528718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51301210-T-G

120528819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51301323-C-T

120528859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51301363-G-A

120528859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51301363-G-T

120528887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51301390-T-C

http://identifiers.org/hco/5/GRCh38#120529252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51301726-C-A

120529337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51301815-T-C

120529370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51301847-A-G

http://identifiers.org/hco/5/GRCh38#120529389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51301862-A-C

120529389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51301862-A-G

120529393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51301866-A-T

120529411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51301888-G-A

http://identifiers.org/hco/5/GRCh38#120529447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51301921-A-C

120529651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51302123-G-A

120529651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51302123-G-T

120529977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51302448-G-A

120538521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51304001-A-G

120538561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51304041-G-A

120538575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51304055-T-G

120538743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51304210-C-T

http://identifiers.org/hco/5/GRCh38#120538760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51304227-A-C

120538782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51304249-G-A

120538813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51304280-C-T

120539116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51304615-A-G

http://identifiers.org/hco/5/GRCh38#120539508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51304944-A-C

120539508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51304944-A-G

120539562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51304995-T-C

120539833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51305180-G-T

120539854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51305201-G-T

120539859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51305206-G-A

120540042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51305319-G-A

120540085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51305362-G-C

http://identifiers.org/hco/5/GRCh38#120540114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51305392-A-C

120540118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51305396-A-G

120540121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51305397-G-A

120540121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51305397-G-T

120540192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51305447-T-C

http://identifiers.org/hco/5/GRCh38#120541607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51307370-A-C

120541682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51307449-A-G

120541739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51307503-G-A

120541739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51307503-G-T

120541951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51307685-C-T

120543322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51313213-C-T

120543353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51313248-G-A

120543353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51313248-G-C

120543623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51313504-G-C

120543838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51313685-T-C

120543879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51313726-G-A

120543941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51313801-C-T

120543944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51313804-A-G

120544160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51314005-G-A

120544281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51314105-G-A

120544298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51314122-C-T

120544314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51314137-G-A

http://identifiers.org/hco/5/GRCh38#120544434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51314239-A-C

http://identifiers.org/hco/5/GRCh38#120544557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51314317-A-C

120544560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51314320-C-T

120545904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51318192-A-G

120545996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51318299-C-G

120546026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51318328-G-A

120546070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51318369-T-C

120546103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51318403-G-A

http://identifiers.org/hco/5/GRCh38#120546125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51318425-C-A

120546266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51318560-G-A

120546272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51318568-T-C

120546410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51318704-C-T

120546482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51318754-C-T

120546543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51318814-T-A

120546559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51318830-A-G

120546702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51318936-G-A

http://identifiers.org/hco/5/GRCh38#120546710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51318944-A-C

120546993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51319195-G-A

120547101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51319340-G-A

120547383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51319598-G-C

120547445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51319670-C-G

120547445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51319670-C-T

120547472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51319698-G-A

http://identifiers.org/hco/5/GRCh38#120547611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51319898-C-A

120547611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51319898-C-T

120547743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51320024-A-G

120547747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51320028-T-G

120547783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51320068-C-G

120547828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51320112-T-G

120547904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51320206-T-C

120547951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51320243-A-G

120547989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51320280-C-G

120548184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51322640-A-G

120548500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51322912-A-G

120548526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51322938-G-A

120548634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51323050-G-C

120548756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51323177-C-G

120548813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51323233-C-G

120548836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51323256-T-A

120548836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51323256-T-G

120548941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51323471-G-A

120549001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51323579-C-T

120549010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51323588-T-C

120549676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51324240-C-T

120549800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51324330-C-G

120549800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51324330-C-T

120550203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51324728-T-A

120550211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51324736-C-G

120550211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51324736-C-T

120550311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51324835-G-A

120550325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51324849-T-C

120550329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51324856-T-C

120550600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51325123-C-G

120550649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51325173-T-A

120550649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51325173-T-C

120550668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51325191-A-T

120550688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51325211-G-A

120550734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51325257-G-A

120550735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51325258-T-C

120550852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51325372-A-T

120550868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51325387-T-C

120550878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51325402-G-A

120550902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51325436-T-C

120550929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51325554-G-A

120550938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51325563-C-G

120550942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51325567-G-A

120550967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51325592-T-C

120551008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51325633-C-T

120551425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51326142-G-T

120551517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51326237-G-A

120551593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51326312-T-G

120551690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51326389-G-C

120551690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51326389-G-T

120551703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51326402-A-T

120552840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51327776-C-T

http://identifiers.org/hco/5/GRCh38#120552872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51327808-C-A

120552947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51327887-T-C

120552966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51327906-T-G

http://identifiers.org/hco/5/GRCh38#120553002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51327941-C-A

120553082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51328173-T-A

120553085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51328176-A-G

120553108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51328201-T-G

120553139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51328234-G-A

120553229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51328323-C-G

120553229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51328323-C-T

120553258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51328344-C-T

120553337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51328431-G-C

120553722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51329219-G-A

120553973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51329428-T-G

120554095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51329550-A-G

http://identifiers.org/hco/5/GRCh38#120554229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51329687-C-A

120554229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51329687-C-T

120557347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51330643-T-C

120557361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51330629-T-C

120557404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51330569-C-T

120557431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51330542-G-C

120557619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51330348-T-C

120557639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51330328-C-T

120557710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51330279-A-G

120557828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51330164-G-T

120557876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51330097-A-T

120565356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51331100-A-G

120565371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51331114-G-C

120565442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51331180-A-G

120565542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51331273-A-G

120565640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: -C-T

120566680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51332926-C-G

http://identifiers.org/hco/5/GRCh38#120566727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51332973-C-A

120566808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51333044-A-G

http://identifiers.org/hco/5/GRCh38#120566867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51333102-C-A

http://identifiers.org/hco/5/GRCh38#120567125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51333364-C-A

120567236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51333477-A-G

120567915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51333748-C-T

120567983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51333816-A-G

120568030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51333896-G-A

120568152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51334008-C-T

120568352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51334206-C-G

120568374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51334228-T-C

120568433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51334287-G-A

120568627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51334473-T-C

http://identifiers.org/hco/5/GRCh38#120568848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51334665-A-C

120568932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51334743-C-T

120568979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51334786-C-G

120569442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51335355-C-T

120569479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51335393-G-A

120569517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51335429-G-T

120569600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51335518-C-G

120569700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51335594-G-T

120569805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51335665-T-A

http://identifiers.org/hco/5/GRCh38#120569883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51335753-A-C

120569988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51335901-C-T

120570131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51336035-A-T

120570144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51336048-A-G

120572304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51339822-A-G

120572410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51339923-T-C

120572533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51340046-G-A

120572536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51340049-A-G

120572590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51340102-A-G

120572705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51340208-G-A

120572822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51340321-G-A

120572924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51340412-T-C

http://identifiers.org/hco/5/GRCh38#120573097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51340575-A-C

120573097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51340575-A-G

120573249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51340716-T-C

120573353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51340806-G-A

120573404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51340855-C-G

120573432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51340883-T-C

120573458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51340906-G-A

120573473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51340921-G-A

120573486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51340933-C-T

120573547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51340990-T-G

120573569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51341012-G-A

120576949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51350139-T-C

120577364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51350640-A-T

120577588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51351346-C-G

120577974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51351673-C-G

120577978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51351677-C-T

120578117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51351829-C-T

http://identifiers.org/hco/5/GRCh38#120578153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51351850-C-A

120582621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51353765-A-G

120582634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51353778-A-G

120582854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51354693-T-C

120582870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51354709-G-A

120582906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51354746-C-T

120582938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51354779-G-C

120583074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51354905-G-T

120583177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51354998-T-A

120583199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51355020-T-C

120583262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51355090-C-T

120583297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51355125-T-A

http://identifiers.org/hco/5/GRCh38#120583312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51355140-A-C

120583505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51355341-A-G

120583531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51355371-G-A

120583531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51355371-G-T

120583660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51355418-A-T

120583760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51355496-A-T

120583804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51355539-G-C

120583804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51355539-G-T

120584201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51356935-G-A

120584243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51356982-C-G

120584498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51357230-C-G

120584540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51357270-A-G

120584572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51357299-C-G

120584573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51357300-C-G

120584776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51357494-T-A

120585113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51360248-C-G

120585122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51360257-G-A

120585858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51360619-C-T

120608226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51367386-G-A

120608313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51367453-T-C

120608313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51367453-T-G

120608515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51367656-G-T

120608537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51367673-A-G

120608616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51367742-G-T

120608959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51368028-G-A

120609000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51368069-C-T

120609026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51368094-A-G

120609094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51368156-T-C

120609691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51370551-G-A

120609708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51370569-C-T

120609760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51370623-T-C

120609772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51370635-C-G

120609874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51370723-A-G

120609900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51370752-T-G

120609961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51370806-C-T

120609986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51370831-A-T

120610027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51370868-T-G

120610038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51370879-C-T

120610068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51370906-G-A

http://identifiers.org/hco/5/GRCh38#120610172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51371018-C-A

120613124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51371517-C-G

120613205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51371606-A-G

120613515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51371914-A-T

120613576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51371970-A-G

120613702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51372080-C-T

120613823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51372178-A-G

120613833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51372188-C-T

120613836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51372191-C-T

120613962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51372317-G-A

120614210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51372560-T-C

120614218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51372568-A-G

120614234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51372585-C-T

120614467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51372824-A-G

120614623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51372935-G-C

120614670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51372982-A-G

120614678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51372990-A-G

120614931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51373232-A-G

120614957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51373259-T-C

120615116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51373399-A-G

120615124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51373406-T-C

120615144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51373426-C-T

120615506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51374665-C-T

120615518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51374677-T-G

120615621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51375012-G-T

120615647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51375038-T-A

120615832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51375208-C-T

120615874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51375243-C-G

120616040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51375407-C-G

120616059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51375426-C-G

120616139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51375669-C-G

120616317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51375834-A-G

120616386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51375905-T-G

120616463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51375977-A-G

120616506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51375997-C-G

120616523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376014-C-T

120616591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376094-G-T

120616642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376140-T-C

120616905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376369-C-G

120616947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376414-T-C

120616948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376415-G-A

120616948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376415-G-T

120616959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376492-A-G

120616961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376494-C-G

120616961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376494-C-T

120616965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376498-A-G

120616965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376498-A-T

120616972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376528-A-G

http://identifiers.org/hco/5/GRCh38#120616995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51376562-C-A

120616995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376562-C-T

120616998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376565-T-C

http://identifiers.org/hco/5/GRCh38#120617004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51376576-C-A

120617004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376576-C-T

120617042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376609-G-A

120617042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376609-G-T

120617071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376639-A-G

120617102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51376668-A-G

http://identifiers.org/hco/5/GRCh38#120617120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51376691-C-A

120617126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51376697-T-G

120617153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51376724-G-A

120617153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51376724-G-C

120617153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51376724-G-T

120617166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51376737-A-G

120617166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51376737-A-T

http://identifiers.org/hco/5/GRCh38#120617201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51376772-C-A

http://identifiers.org/hco/5/GRCh38#120617237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51376806-C-A

120617237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376806-C-T

http://identifiers.org/hco/5/GRCh38#120617262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51376830-C-A

120617294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376861-A-G

http://identifiers.org/hco/5/GRCh38#120617306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51376873-C-A

120617306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376873-C-G

120617403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376960-G-A

120617414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51376972-C-T

http://identifiers.org/hco/5/GRCh38#120617448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51377003-A-C

120617499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51377055-C-T

120617561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51377119-A-G

http://identifiers.org/hco/5/GRCh38#120617566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51377124-A-C

120617590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51377147-T-G

120617635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51377187-T-A

120617670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51377220-G-C

120617699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51377240-A-T

120617844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51377365-C-G

120617844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51377365-C-T

120617882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51377396-C-T

120618132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51377605-G-C

120618187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51377655-A-G

120618234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51377701-T-A

120618298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51377755-G-A

120618298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51377755-G-C

120618298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51377755-G-T

120618338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51377825-G-A

http://identifiers.org/hco/5/GRCh38#120618339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51377826-C-A

120618339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51377826-C-T

120618344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51377837-A-T

120618436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 51378087-T-C

120618440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, splice_acceptor_variant
orthologous variants: 51378091-A-G

120618456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51378107-T-C

http://identifiers.org/hco/5/GRCh38#120618555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51378194-C-A

http://identifiers.org/hco/5/GRCh38#120618593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51378253-C-A

120618593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51378253-C-G

120618593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51378253-C-T

120618602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51378262-T-A

120618626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51378309-G-A

120618626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51378309-G-T

http://identifiers.org/hco/5/GRCh38#120618684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51378375-C-A

120618739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51378532-T-A

120618930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51378892-C-G

120618932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51378894-A-G

120618932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51378894-A-T

120619023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51378995-T-G

120619287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51379248-T-G

120619372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51379335-G-A

http://identifiers.org/hco/5/GRCh38#120619412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51379385-C-A

120619412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51379385-C-T

120619426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51379399-A-G

120619566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51379539-T-A

120619677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51379624-A-G

120619677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51379624-A-T

120619777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51379727-A-T

120619785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51379735-T-C

120619830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51379787-A-G

120619847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51379804-A-G

120620204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51380100-A-G

120620394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51380287-T-C

120620410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51380303-T-C

120620410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51380303-T-G

120620502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51380393-T-A

120622253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51380821-G-A

120622948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51381167-T-C

120622965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51381183-A-G

120623304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51381522-T-G

120623663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51381838-A-G

120623670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51381845-T-G

120625250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51382490-T-C

120625263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51382501-G-T

120625299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51382533-C-T

120625844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51382760-G-A

120625933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51382838-G-A

http://identifiers.org/hco/5/GRCh38#120625943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51382849-A-C

120625943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51382849-A-T

120626220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51383631-A-G

120626294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51383702-C-T

120626298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51383706-C-T

120626493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51383891-C-T

120626578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51383968-T-G

120626619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51384009-G-A

120626846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51384185-T-C

120627031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51384326-A-T

http://identifiers.org/hco/5/GRCh38#120627144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51384433-C-A

120627144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51384433-C-T

120627606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51384868-T-G

120627676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51384939-T-C

120627691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51384954-G-C

120627739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51385003-A-G

120627808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51385064-G-C

120627825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51385081-T-C

120627845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51385098-A-G

120627926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51385182-G-A

120628009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51385251-T-C

120628010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51385252-G-A

120628048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51385287-C-T

120628160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51385405-A-G

120628414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51385667-C-T

120628577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51385829-C-T

http://identifiers.org/hco/5/GRCh38#120630123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51387843-C-A

120630330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51388046-C-T

120630502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51388226-G-A

120630878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51388461-T-C

120630948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51388531-G-A

120631187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51388755-A-G

120638431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51389883-A-G

120638522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51389939-A-G

120638581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51390002-C-T

120638594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51390015-A-T

120638666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51390134-T-C

120638736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51390210-C-T

120638881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51390360-T-C

http://identifiers.org/hco/5/GRCh38#120638960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51390451-C-A

120638962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51390453-G-A

120639046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51390537-G-A

120639149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51390646-T-C

120639298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51390812-T-C

120640320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51391025-T-A

120640443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51391134-C-T

120640531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51391206-G-A

120640531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51391206-G-C

120641002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51391468-G-A

120641002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51391468-G-T

120641127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51391572-G-A

120641192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51391643-T-A

120641239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51391686-G-A

120641340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51391772-A-G

120641500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51391926-T-C

120641846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51392302-A-G

120641863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51392322-T-G

120641870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51392329-G-C

120641900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51392357-T-C

120641918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51392373-G-C

120641918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51392373-G-T

120641945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51392397-C-T

120642048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51392507-A-G

120642094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51392546-C-T

120642193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51392650-G-C

120642257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51392713-G-A

120642257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51392713-G-T

120643073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51394815-T-C

120643139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51394876-C-T

120646130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51395228-G-A

http://identifiers.org/hco/5/GRCh38#120646253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51395331-C-A

120646445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51395545-G-A

120646489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51395587-G-C

120646608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51395696-T-C

120646740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51395798-G-A

120646740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51395798-G-C

120646846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51395972-A-G

120646870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51395996-A-G

120646882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51396008-A-G

120646882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51396008-A-T

http://identifiers.org/hco/5/GRCh38#120646925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51396048-A-C

120646925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51396048-A-G

120646938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51396060-T-G

http://identifiers.org/hco/5/GRCh38#120647156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51396315-A-C

120647164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51396323-G-A

120647170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51396329-G-A

120647206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51396354-G-C

120647258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51396403-A-G

120647313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51396459-C-T

120648157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51397646-G-A

120648158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51397647-T-C

120648187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51397676-G-A

120648187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51397676-G-T

120648193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51397682-A-G

120648451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51399780-C-T

120648500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51399829-C-T

120648755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51399940-T-C

120648777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51399970-C-G

120648777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51399970-C-T

120648803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51399996-T-A

120648831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51400023-T-A

120648831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51400023-T-G

120648847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51400039-C-G

120649009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51400423-A-G

120649405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51400816-C-T

120649461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51400873-A-G

120649570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51400981-G-A

120649615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51401012-A-G

120649758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51401150-A-G

120649765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51401157-T-C

120649778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51401170-T-C

120649830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51401226-A-G

http://identifiers.org/hco/5/GRCh38#120649836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51401232-C-A

120649836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51401232-C-G

120649898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51401291-A-G

120652089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51401462-A-G

http://identifiers.org/hco/5/GRCh38#120652151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51401524-C-A

120652352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51401680-G-A

120653863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51404306-G-C

120653873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51404316-C-T

http://identifiers.org/hco/5/GRCh38#120653949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51404387-C-A

120653998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51404422-A-G

120654012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51404427-C-T

120654092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51404499-G-T

120654175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51404562-G-T

120654244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51404632-C-T

120654434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51404814-T-G

120654981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51405230-A-G

120654986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51405235-C-T

120655038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51405282-C-T

120655140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51405377-G-T

120655192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51405426-G-T

120655263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51405489-A-G

120655279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51405505-G-T

120655880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51405789-C-T

120655914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51405823-A-G

120656024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51405971-A-T

120656375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51408534-C-T

120656642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51409781-T-C

120657128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51410243-G-A

120657161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51410276-C-T

120657302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51411597-G-A

120657302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51411597-G-T

120657314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51411617-C-T

120657800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51412074-T-C

120657829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51412108-T-C

120657831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51412110-C-G

120658175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51412374-A-T

120658201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51412400-G-A

120658201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51412400-G-T

http://identifiers.org/hco/5/GRCh38#120658255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#51412481-A-C

120658270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51412496-G-T

120658409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51412622-G-A

120658409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51412622-G-T

120658492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51412699-G-T

http://identifiers.org/hco/5/GRCh38#120658519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51412729-C-A

120658533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51412743-T-C

120658556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51412765-G-T

http://identifiers.org/hco/5/GRCh38#120658598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51412802-C-A

120658737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51412936-G-A

120658849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51413125-C-T

120658890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51413184-T-C

http://identifiers.org/hco/5/GRCh38#120658928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51413291-C-A

120659008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51413365-C-G

120659008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51413365-C-T

120659060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51413419-A-G

120659082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51413441-C-G

120659252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51413727-G-A

120659252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51413727-G-T

120659326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51413797-G-A

120659880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51415012-T-C

120659880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51415012-T-G

120659966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51415095-G-A

120660023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51415146-A-G

120660157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51415273-G-T

120660184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51415297-C-G

120660494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51415607-A-G

120660906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51415996-T-C

120660906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51415996-T-G

120660970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51416053-T-C

120661100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51416162-C-G

120661336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51416395-A-G

120661349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51416408-G-A

120661349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51416408-G-C

120661410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51416470-T-C

120661491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51416551-A-G

120661659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51416665-C-T

120661718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51416704-G-A

120661793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51416763-C-T

120661933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51417779-A-G

120662011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51417838-T-A

120662011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51417838-T-C

120662017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51417844-C-T

120662186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418006-T-A

120662193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418013-T-C

120662221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418041-T-C

http://identifiers.org/hco/5/GRCh38#120662326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51418143-C-A

120662326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418143-C-T

120662380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418220-C-T

120662382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418222-A-G

120662520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418361-A-G

120662542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418393-C-T

http://identifiers.org/hco/5/GRCh38#120662652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51418495-C-A

http://identifiers.org/hco/5/GRCh38#120662707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51418553-C-A

120662783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418618-G-T

120662805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418637-T-C

120662807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418639-C-T

120662837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418673-G-A

120662848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418676-G-T

120662849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418677-G-C

120662849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418677-G-T

120662900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418709-T-C

http://identifiers.org/hco/5/GRCh38#120663062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51418881-C-A

120663062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418881-C-T

120663105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418903-G-C

120663182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418972-G-A

120663182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418972-G-T

120663190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51418980-T-G

120663222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51419002-G-C

120663222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51419002-G-T

120663227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51419007-T-C

120663316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51419083-G-T

http://identifiers.org/hco/5/GRCh38#120663345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51419112-C-A

120663527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51419282-T-C

120663638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51419398-G-A

120663664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51419456-C-T

120663811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51419624-G-C

120663856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51419673-G-T

120668950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51420236-A-T

120669042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51420330-C-G

120669319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51420611-A-G

120669351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51420636-A-G

120669378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51420662-C-G

120669493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51420789-A-G

120669516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51420812-A-T

120669579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51420862-A-G

http://identifiers.org/hco/5/GRCh38#120669827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51421113-A-C

http://identifiers.org/hco/5/GRCh38#120669831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51421117-C-A

120669926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51421208-A-G

120669926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51421208-A-T

120669951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51421218-A-G

120670093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51421341-A-G

120670206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51421456-T-C

120670258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51421508-A-G

120670344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51421585-T-C

120670433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51421676-C-G

120670454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51421698-A-G

120670454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51421698-A-T

120670551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51421800-C-G

120670551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51421800-C-T

120670664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51421911-T-A

120670712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51421958-G-A

120670749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51421995-A-G

120670763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51422009-C-G

120670962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51422240-C-G

120670962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51422240-C-T

120671228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51422612-A-G

http://identifiers.org/hco/5/GRCh38#120671270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51422659-A-C

120671270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51422659-A-T

120671349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51422796-T-C

120671355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51422802-C-T

120671392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51422841-C-T

120671501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51422938-T-C

120676536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51425831-G-T

http://identifiers.org/hco/5/GRCh38#120676800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51426129-A-C

120676885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51426195-G-C

120676888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51426204-A-G

http://identifiers.org/hco/5/GRCh38#120677029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51426340-A-C

120677108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51426419-G-C

120677264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51426548-G-C

120677406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51426641-C-T

http://identifiers.org/hco/5/GRCh38#120677623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51426850-C-A

120677721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51426954-A-T

http://identifiers.org/hco/5/GRCh38#120678266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51427345-A-C

120678356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51427429-A-T

120678411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51427470-C-T

120678524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51427552-A-G

120680404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51430957-A-G

120680431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51430984-C-T

120680667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51431251-C-T

120680758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51431331-G-A

120680758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51431331-G-T

120680912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51431550-T-C

120680949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51431587-T-C

http://identifiers.org/hco/5/GRCh38#120681958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51432858-C-A

http://identifiers.org/hco/5/GRCh38#120682123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51432978-C-A

120682129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51432984-C-T

120682273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51433120-A-G

120682332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51433178-G-C

120682337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51433181-A-G

120682370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51433222-T-C

120682455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51433296-C-T

http://identifiers.org/hco/5/GRCh38#120682579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51433414-A-C

120682630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51433468-G-A

120682753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51433600-T-C

120682753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51433600-T-G

http://identifiers.org/hco/5/GRCh38#120682828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51433671-C-A

120682911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51433750-C-T

120685837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51435563-T-G

http://identifiers.org/hco/5/GRCh38#120685877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51435603-C-A

120685877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51435603-C-G

120685892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51435618-T-C

120685901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51435627-G-A

120685901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51435627-G-C

120685901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51435627-G-T

http://identifiers.org/hco/5/GRCh38#120685905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51435632-A-C

120685905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51435632-A-G

http://identifiers.org/hco/5/GRCh38#120685906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51435633-C-A

120685914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51435642-G-T

120685915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51435643-G-A

120685915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51435643-G-C

120685915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51435643-G-T

120685998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 51435726-G-A

120685998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 51435726-G-C

120686010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: synonymous variant
orthologous variants: 51435738-T-C

120686100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: synonymous variant
orthologous variants: 51435828-G-A

120686100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: synonymous variant
orthologous variants: 51435828-G-C

120686100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: synonymous variant
orthologous variants: 51435828-G-T

120686274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: synonymous variant
orthologous variants: 51436002-A-T

120686283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: synonymous variant
orthologous variants: 51436011-T-C

http://identifiers.org/hco/5/GRCh38#120686343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51436071-A-C

120686485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: missense variant
orthologous variants: 51436213-G-T

http://identifiers.org/hco/5/GRCh38#120686840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51436578-A-C

120686917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 51436655-A-G

120687002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 51436741-T-A

120687002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 51436741-T-G

120687114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 51436885-T-A

120687326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 51437088-A-G

120687450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51437213-T-A

120687592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51437341-T-A

120687768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51437509-G-A

120687869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51437601-T-A

120688002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51437737-G-C

120688104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51437834-T-A

120688755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51438429-G-A

http://identifiers.org/hco/5/GRCh38#120688762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51438436-C-A

120689169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51438799-T-C

120689169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51438799-T-G

120689348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51438966-T-C

120689811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51439450-T-G

120690751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51440625-G-T

120691449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51441029-T-C

120691559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51441134-A-G

120692126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51442093-A-G

120710871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51463009-G-T

http://identifiers.org/hco/5/GRCh38#120710980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#51463103-C-A

120781171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron variant
orthologous variants: 51525906-G-T

120781231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29654
most severe consequence: intron_variant, undefined
orthologous variants: 51525967-G-T