11483365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 16850524-T-G

11483440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16850450-G-C

11483649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, undefined
orthologous variants: 16850255-C-T

11483709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16850197-T-C

11483711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16850195-T-C

11483724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16850182-G-A

11483726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16850180-G-C

11483732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16850174-G-A

11483735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16850138-G-T

11483738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16850135-C-T

11484089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16849786-G-A

http://identifiers.org/hco/2/GRCh38#11485720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16849292-C-A

11485854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16849193-A-G

11486017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16849046-G-A

11486041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16849022-A-G

11486045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16849018-C-T

11486086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16848983-G-A

11486515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16848758-A-G

11486639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16848673-G-A

11486971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16848313-T-C

11487080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16848208-A-T

11487268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16848017-A-T

11487379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16847911-C-T

11487383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16847899-G-A

http://identifiers.org/hco/2/GRCh38#11487617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16847699-C-A

11487971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16847299-A-G

11487975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16847295-C-T

11487976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16847294-G-A

11488160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16847120-A-G

11488184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16847094-T-C

11488528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16846732-T-A

11488528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16846732-T-C

11489084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16846310-T-A

11489084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16846310-T-C

11489165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16846253-T-C

11493068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16844460-C-T

11498228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16841173-T-C

11498349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16841074-C-T

11499853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16839005-G-C

11507018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16834260-T-G

11507448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16833447-T-A

11507481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16833406-G-A

11507494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16833395-G-C

11507538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16833359-C-T

11507792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16833219-A-T

11508002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16832985-T-C

11508226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16832557-A-G

11508348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16832435-G-T

11508736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16832053-T-A

11511300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16828715-A-T

11511525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16828492-T-C

11511544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16828473-T-C

11513889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16824742-T-C

11513890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16824741-T-C

11514105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16824598-T-A

11514350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16823632-A-G

11514407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16823574-C-T

11514424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16823560-T-C

11514430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16823554-A-G

11514432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16823552-C-T

11514846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16823187-A-T

http://identifiers.org/hco/2/GRCh38#11515120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16822963-A-C

11515160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16822931-T-C

11515301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16822811-A-G

11515424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16822683-T-C

11515714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16822409-A-G

http://identifiers.org/hco/2/GRCh38#11515874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16822254-C-A

11515903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16822224-G-C

11516309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16821962-C-T

11516348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16821923-G-A

11516416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16821829-C-T

11516428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16821817-A-G

11516463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16821781-C-T

11518233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16817467-G-A

11518429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16816888-C-T

http://identifiers.org/hco/2/GRCh38#11518521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16816823-A-C

11518521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16816823-A-G

11518521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16816823-A-T

http://identifiers.org/hco/2/GRCh38#11518611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16816785-A-C

11518745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16816699-T-A

11518745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16816699-T-G

11518755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16816689-A-G

11524468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16815039-C-T

11524764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16814752-C-G

11524821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16814707-A-G

11525002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16814565-C-G

11527808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16814055-T-C

11527931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16813948-T-A

11528044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16813850-A-G

11528056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16813838-C-T

11528752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16813350-G-A

11530444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16811757-T-A

11532033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16811078-G-A

11532050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16811061-A-T

11532160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16810947-T-A

11532222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16810887-A-G

11532516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, undefined
orthologous variants: 16810560-A-G

11532633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16810449-G-T

11532872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, undefined
orthologous variants: 16810222-A-T

11533206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16809916-G-A

11533227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16809900-A-G

11535569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16807174-G-A

11536007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, undefined
orthologous variants: 16806671-G-A

11536163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16806514-G-A

11536271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16806384-C-G

11538103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16804552-C-T

11538139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16804519-C-T

http://identifiers.org/hco/2/GRCh38#11538485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16804230-C-A

11539832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16803448-C-G

11539832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16803448-C-T

11540055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 16803218-A-G

11540113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16803154-G-A

11540113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16803154-G-T

11540159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16803128-G-A

http://identifiers.org/hco/2/GRCh38#11540462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16802810-C-A

11540566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16802713-T-C

11540609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16802663-C-T

11540630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16802641-G-T

http://identifiers.org/hco/2/GRCh38#11540652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#16802619-C-A

11540652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 16802619-C-T

http://identifiers.org/hco/2/GRCh38#11540657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#16802613-C-A

11540741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16802522-G-T

11541003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16802054-A-G

11541163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16801900-T-C

11541277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16801807-G-A

11541326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16801774-A-G

11541563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16801555-A-G

11541716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16801464-C-G

11541828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16801426-G-A

11542314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16801065-G-C

11542362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16801020-G-A

11542542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16800879-G-T

http://identifiers.org/hco/2/GRCh38#11542593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16800830-C-A

11542593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16800830-C-T

http://identifiers.org/hco/2/GRCh38#11542615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16800808-C-A

11542615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16800808-C-G

11542702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16800739-C-T

11542722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16800715-G-A

11542722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16800715-G-T

11542724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16800713-A-G

11542839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16800621-G-T

11543004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16800496-G-C

11543041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16800479-C-T

11546526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16799950-G-A

11546551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16799927-T-C

11546669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16799810-C-G

11546673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16799806-A-G

11548708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16797941-C-T

11548748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16797892-C-G

http://identifiers.org/hco/2/GRCh38#11549259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16797351-C-A

11549363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16797038-G-A

11549632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16796777-C-T

http://identifiers.org/hco/2/GRCh38#11549676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16796736-A-C

11552454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16795837-A-G

11553548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16794084-T-A

11554156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16793469-G-T

11554191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16793437-G-A

11554666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16792766-T-C

11554778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16792602-A-G

11554967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16792164-C-T

11555019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16792105-A-G

11555180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16791939-G-A

11555180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16791939-G-C

11555270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16791844-T-C

http://identifiers.org/hco/2/GRCh38#11555661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16791193-C-A

11555813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16791067-G-A

11555836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16791044-C-T

11556154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16790562-G-A

11556154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16790562-G-C

11556154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16790562-G-T

http://identifiers.org/hco/2/GRCh38#11556215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16790453-C-A

11556215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16790453-C-T

11556393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16790313-C-G

11556393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16790313-C-T

11556678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16789981-A-G

11557571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16789150-A-G

http://identifiers.org/hco/2/GRCh38#11557751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16789031-C-A

11557821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16788961-G-T

11558009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16788777-C-T

11558076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16788702-A-G

11558256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16788609-G-A

11558370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16788451-C-G

11558403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16788418-G-A

11558418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16788388-A-G

11558558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16788242-G-T

11558617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16788188-C-T

11559006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16787791-G-A

11559067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16787729-C-T

11559517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16787333-G-T

11559546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16787310-G-A

11559662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16787199-C-G

11559804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16787073-G-A

11560756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16786376-G-A

http://identifiers.org/hco/2/GRCh38#11561817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16785862-C-A

http://identifiers.org/hco/2/GRCh38#11561900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16785822-C-A

11561900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16785822-C-T

11561914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16785808-G-A

11561914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16785808-G-T

11561976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16785754-A-G

11562232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16785502-A-G

11562322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16785424-G-T

11562336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16785401-A-G

11562342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16785395-G-A

11562342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16785395-G-T

11562378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16785357-G-T

11562382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16785353-G-A

http://identifiers.org/hco/2/GRCh38#11562400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16785334-C-A

11562400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16785334-C-G

http://identifiers.org/hco/2/GRCh38#11562440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16785291-A-C

11562570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16785157-T-C

11562576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16785151-A-G

11562596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16785133-A-G

http://identifiers.org/hco/2/GRCh38#11562672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16785104-C-A

11562714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16785082-G-A

11562714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16785082-G-C

11562714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16785082-G-T

http://identifiers.org/hco/2/GRCh38#11562727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16785069-C-A

11562727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16785069-C-T

11562740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16785056-G-A

11562740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16785056-G-C

11562740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16785056-G-T

11562769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16785051-A-T

11562802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16785021-T-C

11562829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16785009-G-T

11562843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16784995-T-A

11562843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16784995-T-C

11562843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16784995-T-G

11562849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16784989-T-A

11562849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16784989-T-G

http://identifiers.org/hco/2/GRCh38#11562976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16784878-C-A

11566468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16783465-C-T

11566661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16783272-G-A

http://identifiers.org/hco/2/GRCh38#11566685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16783252-C-A

11566693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16783244-G-A

11566693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16783244-G-T

11566719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16783220-G-A

11566719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16783220-G-T

http://identifiers.org/hco/2/GRCh38#11566722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16783217-C-A

11566722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16783217-C-T

11566748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16783198-G-A

11566748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16783198-G-T

11566813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16783148-T-C

http://identifiers.org/hco/2/GRCh38#11567418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16782567-C-A

11567456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16782532-G-A

11567862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16782158-C-T

http://identifiers.org/hco/2/GRCh38#11567984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16782056-C-A

11568137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16781940-C-T

11568611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16781517-G-A

11568611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16781517-G-C

11568947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16781145-C-T

11568962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16781130-C-T

11569305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16780781-T-C

11569417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16780632-G-A

11569417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16780632-G-T

11569466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16780600-A-G

11569497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16780571-G-A

11569580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16780474-T-G

11569832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16780273-G-T

http://identifiers.org/hco/2/GRCh38#11572663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16778735-A-C

11572765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16778643-G-A

11572765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16778643-G-T

11572906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16778536-C-G

11573008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16778424-G-A

11573044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16778389-C-T

11573113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16778330-C-G

11573113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16778330-C-T

11573146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16778297-T-C

11573207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16778250-C-T

11573319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16778140-G-C

11573319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16778140-G-T

11573390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16778082-C-T

11573392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16778080-C-G

11573487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16777998-T-C

11573573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16777892-G-A

11573590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16777869-G-A

http://identifiers.org/hco/2/GRCh38#11573633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16777837-A-C

11573633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16777837-A-G

11574022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16777535-C-T

http://identifiers.org/hco/2/GRCh38#11574026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16777531-C-A

11574106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16777457-G-C

11574192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16777398-G-T

11574198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16777392-C-T

http://identifiers.org/hco/2/GRCh38#11574283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16777324-A-C

11574355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16777257-G-T

11574659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16777006-C-T

11574937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16776762-G-C

11575313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16776399-G-C

11575352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16776358-A-T

11575365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16776345-C-T

11575502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16776215-G-T

11575988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16775089-G-A

http://identifiers.org/hco/2/GRCh38#11576344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16774950-C-A

11576344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16774950-C-G

11576614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16774752-G-C

11576614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16774752-G-T

http://identifiers.org/hco/2/GRCh38#11576636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16774741-C-A

11576636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16774741-C-G

11577282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16774425-G-A

11577305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16774402-G-A

11577310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16774397-C-T

11577355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16774352-A-G

11577554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16774191-G-A

11577554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16774191-G-T

11577613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16774109-G-C

11577665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16774065-C-G

11577665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16774065-C-T

11577759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16773962-G-T

11577843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16773878-T-C

11577982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16773755-C-T

11578035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16773696-G-A

11578044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16773683-T-C

11578082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16773646-T-G

11578169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16773560-G-A

11578169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16773560-G-T

11578171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16773558-G-T

11578226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16773505-C-T

11578227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16773504-T-C

11578345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16773385-T-A

11578362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16773368-A-G

11578473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16773248-G-A

11578473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16773248-G-C

11578473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16773248-G-T

11578476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16773245-G-A

11578477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16773244-G-A

11578477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16773244-G-T

11578618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16773098-T-C

11578756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16772977-G-C

11579641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16772115-G-A

11579876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16771896-G-A

11579876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16771896-G-T

11580492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16771149-G-A

http://identifiers.org/hco/2/GRCh38#11580561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16771087-C-A

11580561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16771087-C-G

11580561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16771087-C-T

11580599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16771047-G-A

11580599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16771047-G-T

11580861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 16770817-G-A

http://identifiers.org/hco/2/GRCh38#11580887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16770792-C-A

11580942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, missense_variant
orthologous variants: 16770738-T-A

http://identifiers.org/hco/2/GRCh38#11580971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16770717-C-A

11580971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, missense_variant
orthologous variants: 16770717-C-T

11580991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, missense_variant
orthologous variants: 16770699-G-A

11580991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, missense_variant
orthologous variants: 16770699-G-T

11581057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16770635-G-A

11581061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16770631-T-C

11581105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16770589-A-G

11581132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16770571-G-A

11581132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16770571-G-T

http://identifiers.org/hco/2/GRCh38#11581133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16770570-C-A

11581133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16770570-C-G

11581133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16770570-C-T

http://identifiers.org/hco/2/GRCh38#11581249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16770491-A-C

11581278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16770464-G-T

http://identifiers.org/hco/2/GRCh38#11581279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16770463-C-A

11581279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16770463-C-T

11581280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16770462-T-C

http://identifiers.org/hco/2/GRCh38#11581391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16770353-C-A

11581391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16770353-C-G

11581391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16770353-C-T

11581413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16770334-T-C

11581413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16770334-T-G

11581672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16770154-C-T

11581708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16770102-T-C

11581710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16770100-G-T

11581797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16769969-C-T

11581877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16769930-C-T

11582171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16769676-C-G

11582247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16769575-C-G

11582247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16769575-C-T

11582454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16769399-C-G

11582454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16769399-C-T

11582878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, undefined
orthologous variants: 16769116-A-G

11582947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16769067-G-C

11583279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16768855-G-A

11583282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16768852-G-A

11583340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16768796-T-G

11583555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16768589-G-T

11583606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, undefined
orthologous variants: 16768573-T-A

11584181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16768100-G-T

11584195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, undefined
orthologous variants: 16768087-G-A

11584211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16768071-C-T

11584608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16767735-G-A

11584632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, undefined
orthologous variants: 16767710-G-A

11584646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, undefined
orthologous variants: 16767696-T-C

11584698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16767636-T-C

11584739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16767604-G-A

11584739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16767604-G-T

11585077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16767371-G-A

11585077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16767371-G-C

11585077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16767371-G-T

11585121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16767329-T-A

11585121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16767329-T-C

11585121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16767329-T-G

http://identifiers.org/hco/2/GRCh38#11585123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16767327-C-A

11585382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16767073-G-A

11585382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16767073-G-T

11585406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16767061-T-C

11585412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16767055-G-T

11585936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16766596-A-G

11585937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16766595-T-G

11585951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16766581-G-A

11586026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16766515-A-G

11586091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16766465-T-G

11586213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16766358-T-C

11586213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16766358-T-G

11587067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16766055-G-A

11587093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16766028-G-C

11587189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16765991-G-A

11587261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16765937-T-A

11587261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16765937-T-C

11587261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16765937-T-G

11587326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16765896-A-G

11587430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, missense_variant
orthologous variants: 16765816-C-T

http://identifiers.org/hco/2/GRCh38#11587465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16765774-C-A

http://identifiers.org/hco/2/GRCh38#11588463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16765253-C-A

11588466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16765250-T-C

11588473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16765235-A-G

11588505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16765205-G-T

http://identifiers.org/hco/2/GRCh38#11588517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16765193-C-A

11588535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16765178-C-T

http://identifiers.org/hco/2/GRCh38#11588554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16765159-C-A

http://identifiers.org/hco/2/GRCh38#11588561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16765150-C-A

http://identifiers.org/hco/2/GRCh38#11588562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16765149-A-C

http://identifiers.org/hco/2/GRCh38#11588593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16765117-C-A

11588593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16765117-C-T

http://identifiers.org/hco/2/GRCh38#11588595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16765115-C-A

11588595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16765115-C-T

http://identifiers.org/hco/2/GRCh38#11588640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16765057-C-A

11588642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16765055-G-A

11588642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16765055-G-T

11588976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16764737-A-G

http://identifiers.org/hco/2/GRCh38#11589953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16764191-C-A

11589979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16764166-T-C

11590232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16763929-C-T

11592695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16762135-G-A

11592695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16762135-G-C

11592695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16762135-G-T

11592710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16762128-T-A

11592711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16762127-G-A

11592711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16762127-G-T

http://identifiers.org/hco/2/GRCh38#11592760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16762038-C-A

11592760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16762038-C-T

11592830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16761968-G-T

11592835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16761963-G-A

11592835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: stop gained
orthologous variants: 16761963-G-T

http://identifiers.org/hco/2/GRCh38#11592841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16761957-C-A

11592841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16761957-C-T

http://identifiers.org/hco/2/GRCh38#11592888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16761910-C-A

11592888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16761910-C-G

11592888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: synonymous variant
orthologous variants: 16761910-C-T

http://identifiers.org/hco/2/GRCh38#11592893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16761905-C-A

11593096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16761702-G-A

11593149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16761646-G-A

11593178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16761618-G-A

11593238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16761564-G-A

11593238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16761564-G-T

11593389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16761365-T-C

11593399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16761355-G-C

11593415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16761330-C-G

11595265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16760385-C-T

11595407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16760254-T-C

11595420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16760241-A-T

11595445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16760214-G-A

11595548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16760121-T-A

11595599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16760072-T-A

11595962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16759693-G-A

11595962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16759693-G-T

http://identifiers.org/hco/2/GRCh38#11595986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16759670-C-A

11595986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16759670-C-T

11596016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16759645-A-G

http://identifiers.org/hco/2/GRCh38#11596197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16759473-A-C

11596224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16759446-A-G

11596346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16759392-T-G

11596347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16759391-G-A

11596347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16759391-G-T

11596365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16759381-G-T

11596385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16759361-G-T

11596420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16759321-G-A

11596420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16759321-G-T

11597406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16759009-A-T

11597407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16759008-C-G

11597408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16759007-T-C

11597427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16758988-T-C

11597645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16758858-A-T

http://identifiers.org/hco/2/GRCh38#11597701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16758811-C-A

11597807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16758723-C-T

11597825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16758705-G-A

11597986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 16758541-G-A

11597986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 16758541-G-T

11598017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16758519-C-T

11598052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16758481-A-G

11598569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16758070-T-C

11598570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16758069-G-A

11598570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16758069-G-T

11598613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16758033-G-A

11598613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16758033-G-C

11598881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16757782-G-T

11598958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16757739-T-A

11598958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16757739-T-C

http://identifiers.org/hco/2/GRCh38#11599029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16757666-A-C

11599029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16757666-A-G

11600217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16757115-C-T

11600235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16757097-T-C

http://identifiers.org/hco/2/GRCh38#11600334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16757002-C-A

http://identifiers.org/hco/2/GRCh38#11600383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16756953-A-C

11600383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16756953-A-G

11600391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16756946-A-G

11600454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16756752-T-C

11600503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16756662-C-T

11600734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16756360-T-G

http://identifiers.org/hco/2/GRCh38#11600736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16756358-C-A

11600736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16756358-C-T

http://identifiers.org/hco/2/GRCh38#11601019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16756079-C-A

http://identifiers.org/hco/2/GRCh38#11601101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16756001-C-A

11601101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16756001-C-T

http://identifiers.org/hco/2/GRCh38#11601123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16755979-C-A

11601317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16755809-G-A

11601324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16755801-G-A

11601759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16755298-G-A

11602298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16754669-G-A

11602298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16754669-G-T

11602352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16754615-T-C

11602365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16754602-G-A

11602365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16754602-G-T

11602463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 16754508-T-A

11602463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 16754508-T-G

11602585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16754395-T-A

11610030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16753825-C-T

11610131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16753735-A-T

11610505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16753029-G-A

http://identifiers.org/hco/2/GRCh38#11610673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16752678-C-A

11610673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16752678-C-T

http://identifiers.org/hco/2/GRCh38#11610932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16752419-C-A

11610932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 16752419-C-T

11610989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 16752362-G-T

11611084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16752276-G-T

http://identifiers.org/hco/2/GRCh38#11611162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16752222-C-A

11611162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16752222-C-T

11611194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16752189-C-T

11611215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16752167-C-T

11611217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16752165-C-T

11611278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16752116-G-T

11611871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16751819-C-T

11611897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16751787-A-G

11611907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16751777-C-T

http://identifiers.org/hco/2/GRCh38#11612311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16751694-C-A

11612311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16751694-C-T

11612388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16751627-T-A

11612388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16751627-T-C

11612516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16751254-G-A

11612634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16751137-G-A

11612634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16751137-G-C

11612634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16751137-G-T

11612635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16751136-G-T

11612636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16751135-G-T

11614838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16749941-C-T

http://identifiers.org/hco/2/GRCh38#11614896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16749868-C-A

http://identifiers.org/hco/2/GRCh38#11615012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16749763-C-A

11615012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16749763-C-T

11615049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16749729-G-A

11615049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16749729-G-C

11615049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16749729-G-T

http://identifiers.org/hco/2/GRCh38#11615057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16749721-C-A

11615057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16749721-C-T

11615194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16749588-G-A

11615194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16749588-G-T

11615257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16749525-A-G

11615269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16749516-G-A

11615269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16749516-G-C

http://identifiers.org/hco/2/GRCh38#11615339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16749473-C-A

11615638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16749283-C-T

11615902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16749057-T-C

11615939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16749033-G-T

11615981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16749017-G-A

11616485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16748773-T-G

11616487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16748771-G-A

11616487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16748771-G-C

11616544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16748711-G-T

11616636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16748625-A-G

11616654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16748607-C-G

http://identifiers.org/hco/2/GRCh38#11616758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16748508-C-A

11616771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16748498-T-G

11616808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16748467-G-T

http://identifiers.org/hco/2/GRCh38#11616815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16748460-C-A

11616815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16748460-C-G

http://identifiers.org/hco/2/GRCh38#11616861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16748426-C-A

11616861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16748426-C-G

11616898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16748380-G-A

11617001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16748285-C-T

11617084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16748207-A-G

11617569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16747274-G-A

11617569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16747274-G-T

11617758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16747134-G-A

11617759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16747133-A-G

11617759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16747133-A-T

11617762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16747130-G-A

11618256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16746866-G-A

11618260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16746862-G-A

11618313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: synonymous variant
orthologous variants: 16746808-G-A

11618313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: synonymous variant
orthologous variants: 16746808-G-T

11618360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16746761-A-G

11618398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16746723-G-A

11618398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16746723-G-C

11618457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: synonymous variant
orthologous variants: 16746667-C-T

11618524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16746600-T-C

11618570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16746557-C-T

http://identifiers.org/hco/2/GRCh38#11618887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16746240-C-A

11618887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16746240-C-T

http://identifiers.org/hco/2/GRCh38#11618972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16746151-C-A

11618972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16746151-C-T

11620806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16742879-A-T

http://identifiers.org/hco/2/GRCh38#11620832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16742859-C-A

http://identifiers.org/hco/2/GRCh38#11620855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16742835-A-C

11620879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16742812-G-A

11621014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 16742677-T-C

11621128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16742558-A-G

11621389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16742307-G-A

http://identifiers.org/hco/2/GRCh38#11621482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16742210-C-A

11621616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16742077-G-T

11621824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16741886-C-T

11622430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16741614-A-G

11622463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16741552-C-T

11622634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16741376-A-G

11622704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16741318-G-C

11622716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16741307-G-C

http://identifiers.org/hco/2/GRCh38#11623040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16740996-A-C

11625661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16739328-G-A

11625661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16739328-G-C

11625661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16739328-G-T

11626684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16738902-A-G

11626810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16738795-T-G

11627063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16738537-G-A

11627143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16738430-G-A

11627304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16738276-G-C

11627333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16738255-C-T

11627467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16738138-T-C

11627532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16738090-T-C

11627623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16738003-T-A

11627627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16737999-T-C

11627753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16737897-C-G

11628027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16737463-G-A

11628094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16737434-G-C

11628366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16737197-G-A

11628459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16737094-C-T

11628681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16736412-T-C

11629064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16735974-A-G

11629129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16735867-A-G

11629331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16735671-C-T

11629615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16734806-A-G

11629761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16734685-G-A

11629829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16734643-T-C

11629855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16734617-A-G

11629855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16734617-A-T

http://identifiers.org/hco/2/GRCh38#11629868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16734604-C-A

11629892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16734579-T-C

11629894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16734577-T-A

11629914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16734557-G-A

11629936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16734535-C-G

11629936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16734535-C-T

11630050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 16734420-G-A

11630246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16734218-G-A

11630246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16734218-G-C

11630246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16734218-G-T

11630254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16734210-T-C

11630254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16734210-T-G

11630378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16734097-G-T

11630473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16733788-C-T

http://identifiers.org/hco/2/GRCh38#11630566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16733693-A-C

11630638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16733629-G-T

11630732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16733419-C-T

11630827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16733324-G-A

11631069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16733095-C-T

http://identifiers.org/hco/2/GRCh38#11631132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16733049-C-A

11631132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16733049-C-T

11631414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16732805-A-G

11631457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16732766-T-C

11631764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16732460-T-A

11631764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16732460-T-C

http://identifiers.org/hco/2/GRCh38#11631777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16732447-C-A

11631777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16732447-C-T

11631803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16732426-G-A

11631803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16732426-G-T

11631808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16732421-G-A

11631808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16732421-G-T

11631819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16732411-T-C

11631819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16732411-T-G

11631820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16732410-T-C

11631930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 16732310-C-T

11631945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 16732295-A-G

11632107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16732133-G-A

11632110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16732130-G-A

11632133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16732109-A-G

11632133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16732109-A-T

11632174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16732067-T-A

11632841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16731552-G-A

11632841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16731552-G-T

11632846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16731547-G-A

11632846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16731547-G-T

http://identifiers.org/hco/2/GRCh38#11632969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16731423-A-C

http://identifiers.org/hco/2/GRCh38#11633209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16731252-A-C

11633209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16731252-A-G

11633707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16730857-A-G

11633925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16730644-G-A

http://identifiers.org/hco/2/GRCh38#11633964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16730584-C-A

11633964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16730584-C-T

11633984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16730564-G-A

11633984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16730564-G-T

http://identifiers.org/hco/2/GRCh38#11634035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16730498-C-A

11634035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16730498-C-T

http://identifiers.org/hco/2/GRCh38#11634064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16730478-C-A

11634228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16730320-C-T

11634254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: synonymous variant
orthologous variants: 16730294-C-T

11634276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16730272-T-C

11634365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16730181-T-C

11634420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16730131-G-C

11634420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16730131-G-T

11635216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16727876-C-T

11635280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16727812-G-A

11635420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16727669-G-A

11635420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16727669-G-T

11635423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16727666-G-A

11635472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16727619-G-A

11635472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16727619-G-T

11635517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16727573-G-A

11635537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16727561-G-A

11635537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16727561-G-T

11635748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16727371-G-C

11636088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16727060-G-A

11636089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16727059-G-A

11636110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16727036-T-G

11636171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16726986-C-T

11636324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16726822-A-G

11636619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16726316-G-T

11637716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 16724809-G-A

11637716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 16724809-G-C

11637773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16724752-A-G

http://identifiers.org/hco/2/GRCh38#11637863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16724662-A-C

11637997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16724556-A-G

11637997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16724556-A-T

11638290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16724289-G-T

11638378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16724202-G-T

11638387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16724193-C-T

11638388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16724192-G-A

11638399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16724180-C-T

11638451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16724118-G-A

11638460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16724100-A-G

http://identifiers.org/hco/2/GRCh38#11638519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16724033-A-C

11638519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16724033-A-T

11638568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16723979-G-A

11638568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16723979-G-T

11638580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16723967-A-G

11638580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16723967-A-T

11638613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16723940-A-G

http://identifiers.org/hco/2/GRCh38#11638834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16723723-C-A

11638834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16723723-C-T

http://identifiers.org/hco/2/GRCh38#11638916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16723641-C-A

http://identifiers.org/hco/2/GRCh38#11638924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16723633-C-A

11639095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16723477-C-T

11639199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16723394-C-T

11639803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16722985-G-A

11639803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16722985-G-T

11640010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16722787-C-T

11640019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16722778-C-T

11640060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16722746-T-C

11640140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16722677-A-G

http://identifiers.org/hco/2/GRCh38#11640160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16722658-C-A

11640160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16722658-C-T

11640232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16722602-G-A

11640232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16722602-G-C

11640232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16722602-G-T

http://identifiers.org/hco/2/GRCh38#11640251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16722582-C-A

11640251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: intron variant
orthologous variants: 16722582-C-G

11640337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: missense variant
orthologous variants: 16722496-G-C

11640489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3 prime UTR variant
orthologous variants: 16722342-G-A

http://identifiers.org/hco/2/GRCh38#11640609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#16722218-C-A

11640609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3 prime UTR variant
orthologous variants: 16722218-C-T

11640707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3 prime UTR variant
orthologous variants: 16722135-G-A

11640707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3 prime UTR variant
orthologous variants: 16722135-G-T

11640906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24885
most severe consequence: 3 prime UTR variant
orthologous variants: 16721956-C-T